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"Ribavirin"

Review

Hepatitis E as a trigger for acute-on-chronic liver failure
Maria Buti, Juan Carlos Ruiz-Cobo, Rafael Esteban, Mar Riveiro-Barciela
Clin Mol Hepatol 2025;31(Suppl):S196-S204.
Published online November 11, 2024
DOI: https://doi.org/10.3350/cmh.2024.0758
Acute hepatitis E virus (HEV) infection is typically self-limiting and has a favourable prognosis. However, certain populations such as patients with pre-existing chronic liver disease may experience severe manifestations, including progression to acute-on-chronic liver failure (ACLF). Among viral hepatitis types, hepatitis A, E, and B are major causes of ACLF. Active screening and early diagnosis of HEV infection in patients with cirrhosis, especially those who develop ACLF, can improve management and enable timely antiviral therapy. Preventive measures, including HEV vaccination for high-risk groups, could reduce the morbidity and mortality associated with hepatitis E.

Citations

Citations to this article as recorded by  Crossref logo
  • Efficacy and safety of mesenchymal stem cell therapy in acute on chronic liver failure: a systematic review and meta-analysis of randomized controlled clinical trials
    Wenming Lu, Longxiang Yan, Lulu Peng, Xuesong Wang, Xingkun Tang, Jing Du, Jing Lin, Zhengwei Zou, Lincai Li, Junsong Ye, Lin Zhou
    Stem Cell Research & Therapy.2025;[Epub]     CrossRef
  • Hepatitis A and E Viruses Are Important Agents of Acute Severe Hepatitis in Asia: A Narrative Review
    Reina Sasaki-Tanaka, Tatsuo Kanda, Takeshi Yokoo, Hiroyuki Abe, Kazunao Hayashi, Akira Sakamaki, Hiroteru Kamimura, Shuji Terai
    Pathogens.2025; 14(5): 454.     CrossRef
  • The role of bacterial outer membrane vesicles in inflammatory response of acute-on-chronic liver failure
    Xiaojing Qin, Shuang Wang, Zhanyao Yan, Ninghui Zhao, Jia Yao
    Frontiers in Microbiology.2025;[Epub]     CrossRef
  • Ribavirina como tratamiento de hepatitis E aguda grave sobre hepatopatía crónica: experiencia clínica
    Alba Rabadán Mata, María Dolores Antón Conejero, José María Paredes Arquiola
    Medicina Clínica.2025; 165(6): 107187.     CrossRef
  • Ribavirin as a treatment for severe acute hepatitis E on chronic liver disease: Clinical experience
    Alba Rabadán Mata, María Dolores Antón Conejero, José María Paredes Arquiola
    Medicina Clínica (English Edition).2025; : 107187.     CrossRef
  • 5,577 View
  • 171 Download
  • 4 Web of Science
  • Crossref

Original Articles

Viral hepatitis

Sofosbuvir/velpatasvir plus ribavirin for Child-Pugh B and Child-Pugh C hepatitis C virus-related cirrhosis
Chen-Hua Liu, Chi-Yi Chen, Wei-Wen Su, Chun-Jen Liu, Ching-Chu Lo, Ke-Jhang Huang, Jyh-Jou Chen, Kuo-Chih Tseng, Chi-Yang Chang, Cheng-Yuan Peng, Yu-Lueng Shih, Chia-Sheng Huang, Wei-Yu Kao, Sheng-Shun Yang, Ming-Chang Tsai, Jo-Hsuan Wu, Po-Yueh Chen, Pei-Yuan Su, Jow-Jyh Hwang, Yu-Jen Fang, Pei-Lun Lee, Chi-Wei Tseng, Fu-Jen Lee, Hsueh-Chou Lai, Tsai-Yuan Hsieh, Chun-Chao Chang, Chung-Hsin Chang, Yi-Jie Huang, Jia-Horng Kao
Clin Mol Hepatol 2021;27(4):575-588.
Published online July 13, 2021
DOI: https://doi.org/10.3350/cmh.2021.0155
Background/Aims
Real-world studies assessing the effectiveness and safety of sofosbuvir/velpatasvir (SOF/VEL) plus ribavirin (RBV) for Child-Pugh B/C hepatitis C virus (HCV)-related cirrhosis are limited.
Methods
We included 107 patients with Child-Pugh B/C HCV-related cirrhosis receiving SOF/VEL plus RBV for 12 weeks in Taiwan. The sustained virologic response rates at off-treatment week 12 (SVR12) for the evaluable population (EP), modified EP, and per-protocol population (PP) were assessed. Thesafety profiles were reported.
Results
The SVR12 rates in the EP, modified EP and PP were 89.7% (95% confidence interval [CI], 82.5–94.2%), 94.1% (95% CI, 87.8–97.3%), and 100% (95% CI, 96.2–100%). Number of patients who failed to achieve SVR12 were attributed to virologic failures. The SVR12 rates were comparable regardless of patient characteristics. One patient discontinued treatment because of adverse events (AEs). Twenty-four patients had serious AEs and six died, but none were related to SOF/VEL or RBV. Among the 96 patients achieving SVR12, 84.4% and 64.6% had improved Child-Pugh and model for endstage liver disease (MELD) scores. Multivariate analysis revealed that a baseline MELD score ≥15 was associated with an improved MELD score of ≥3 (odds ratio, 4.13; 95% CI, 1.16–14.71; P=0.02). Patients with chronic kidney disease (CKD) stage 1 had more significant estimated glomerular filtration rate declines than patients with CKD stage 2 (-0.42 mL/min/1.73 m2/month; P=0.01) or stage 3 (-0.56 mL/min/1.73 m2/month; P<0.001).
Conclusions
SOF/VEL plus RBV for 12 weeks is efficacious and well-tolerated for Child-Pugh B/C HCV-related cirrhosis.

Citations

Citations to this article as recorded by  Crossref logo
  • Role of etiological therapy in achieving recompensation of decompensated liver cirrhosis
    Dmitry V Garbuzenko
    World Journal of Hepatology.2025;[Epub]     CrossRef
  • Effectiveness of etiotropic therapy in achieving recompensation of cirrhosis
    D.V. Garbuzenco
    Russian Journal of Evidence-Based Gastroenterology.2025; 14(2): 68.     CrossRef
  • Real-World Treatment Efficacy and Safety Profile of Sofosbuvir- and Velpatasvir-Based HCV Treatment in South Korea: Multicenter Prospective Study
    Jae Hyun Yoon, Chang Hun Lee, Hoon Gil Jo, Ju-Yeon Cho, Jin Dong Kim, Jin Won Kim, Ga Ram You, Sung Bum Cho, Sung Kyu Choi
    Viruses.2025; 17(7): 949.     CrossRef
  • Efficacy and Safety of Velpatasvir Plus Sofosbuvir With or Without Ribavirin in Hepatitis C Patients With Decompensated Cirrhosis: A Systematic Review and Meta‐Analysis
    Jing Xiao, Xinnian Zhang, Xiaozhou Mao, Shunhao Lai, Shuangli Li, Yunjian Sheng
    Journal of Viral Hepatitis.2025;[Epub]     CrossRef
  • Oral carbohydrate intake before selective laparoscopic liver resection reduces insulin resistance and enhances recovery
    Hongqiong Li
    American Journal of Translational Research.2025; 17(8): 6080.     CrossRef
  • Recent Advances in the Treatment of Chronic Hepatitis C
    Suk Bae Kim
    The Korean Journal of Gastroenterology.2025; 85(4): 475.     CrossRef
  • Five-year follow-up of sustained virological response with hepatitis C infection after direct-acting antiviral therapy: A single-center retrospective study
    Mengyue Li, Yiting Li, Ying Zhang, Xiangyang Wang, Chaoshuang Lin
    Medicine.2024; 103(7): e37212.     CrossRef
  • Cutting-edge pharmacotherapy for hepatitis C virus infection: a comprehensive review
    Chen-Hua Liu, Yu-Ping Chang, Jia-Horng Kao
    Expert Opinion on Pharmacotherapy.2024; 25(12): 1691.     CrossRef
  • Real-life study on the effectiveness and safety of sofosbuvir/velpatasvir-based antiviral agents for hepatitis C eradication in Chinese patients
    Jiayi Wang, Lingyao Du, Dongmei Zhang, Chen Zhou, Yilan Zeng, Miao Liu, Xing Cheng, Xiaona Song, Han Chen, Ning Han, Enqiang Chen, Hong Tang
    Journal of Virus Eradication.2024; 10(4): 100571.     CrossRef
  • Sofosbuvir/velpatasvir or glecaprevir/pibrentasvir for treating patients with hepatitis C virus reinfection following direct‐acting antiviral‐induced sustained virologic response
    Chen‐Hua Liu, Chun‐Jen Liu, Tung‐Hung Su, Tai‐Chung Tseng, Pei‐Jer Chen, Jia‐Horng Kao
    Advances in Digestive Medicine.2023; 10(1): 34.     CrossRef
  • Changes in renal function in patients with chronic hepatitis C treated with sofosbuvir‐velpatasvir
    Pei‐Kai Su, Te‐Sheng Chang, Shui‐Yi Tung, Kuo‐Liang Wei, Chien‐Heng Shen, Yung‐Yu Hsieh, Wei‐Ming Chen, Yi‐Hsing Chen, Chun‐Hsien Chen, Chih‐Wei Yen, Huang‐Wei Xu, Wei‐Ling Tung, Kao‐Chi Chang
    Advances in Digestive Medicine.2023; 10(3): 150.     CrossRef
  • Response to antiviral therapy for chronic hepatitis C and risk of hepatocellular carcinoma occurrence in Japan: a systematic review and meta-analysis of observational studies
    Yoko Yamagiwa, Keitaro Tanaka, Keitaro Matsuo, Keiko Wada, Yingsong Lin, Yumi Sugawara, Tetsuya Mizoue, Norie Sawada, Hidemi Takimoto, Hidemi Ito, Tetsuhisa Kitamura, Ritsu Sakata, Takashi Kimura, Shiori Tanaka, Manami Inoue, Sarah Krull Abe, Shuhei Nomur
    Scientific Reports.2023;[Epub]     CrossRef
  • Efficacy and safety of sofosbuvir–velpatasvir and sofosbuvir–velpatasvir–voxilaprevir for hepatitis C in Korea: a Phase 3b study
    Jeong Heo, Yoon Jun Kim, Sung Wook Lee, Youn-Jae Lee, Ki Tae Yoon, Kwan Soo Byun, Yong Jin Jung, Won Young Tak, Sook-Hyang Jeong, Kyung Min Kwon, Vithika Suri, Peiwen Wu, Byoung Kuk Jang, Byung Seok Lee, Ju-Yeon Cho, Jeong Won Jang, Soo Hyun Yang, Seung W
    The Korean Journal of Internal Medicine.2023; 38(4): 504.     CrossRef
  • Efficacy and Safety of Sofosbuvir/Velpatasvir Plus Ribavirin in Patients with Hepatitis C Virus-Related Decompensated Cirrhosis
    Steven Flamm, Eric Lawitz, Brian Borg, Michael Charlton, Charles Landis, K. Rajender Reddy, Mitchell Shiffman, Angel Alsina, Charissa Chang, Natarajan Ravendhran, Candido Hernandez, Christophe Hézode, Stacey Scherbakovsky, Renee-Claude Mercier, Didier Sam
    Viruses.2023; 15(10): 2026.     CrossRef
  • Sofosbuvir-based direct-acting antivirals for patients with decompensated hepatitis C virus–related cirrhosis
    Chen-Hua Liu, Chun-Jen Liu, Jia-Horng Kao
    Journal of the Chinese Medical Association.2022; 85(5): 647.     CrossRef
  • Real-life experience of ledipasvir and sofosbuvir for HCV infected Korean patients: a multicenter cohort study
    Soon Kyu Lee, Sung Won Lee, Hae Lim Lee, Hee Yeon Kim, Chang Wook Kim, Do Seon Song, U Im Chang, Jin Mo Yang, Sun Hong Yoo, Jung Hyun Kwon, Soon Woo Nam, Seok-Hwan Kim, Myeong Jun Song, Jaejun Lee, Hyun Yang, Si Hyun Bae, Ji Won Han, Heechul Nam, Pil Soo
    The Korean Journal of Internal Medicine.2022; 37(6): 1167.     CrossRef
  • HCV Infection and Liver Cirrhosis Are Associated with a Less-Favorable Serum Cholesteryl Ester Profile Which Improves through the Successful Treatment of HCV
    Kilian Weigand, Georg Peschel, Jonathan Grimm, Martina Müller, Marcus Höring, Sabrina Krautbauer, Gerhard Liebisch, Christa Buechler
    Biomedicines.2022; 10(12): 3152.     CrossRef
  • 13,553 View
  • 1,029 Download
  • 15 Web of Science
  • Crossref

Viral hepatitis

Influence of some methylated hepatocarcinogenesis-related genes on the response to antiviral therapy and development of fibrosis in chronic hepatitis C patients
Waleed Seif Eldin Mohamed Mostafa, Mohammed Hassan Saiem Al-Dahr, Dalia Abdel Hamid Omran, Zeinab Fathy Abdullah, Suzan Hamdy Elmasry, Mohamed Nabil Ibrahim
Clin Mol Hepatol 2020;26(1):60-69.
Published online October 22, 2019
DOI: https://doi.org/10.3350/cmh.2019.0051
Epigenetics involved in multiple normal cellular processes. Previous research have revealed the role of hepatitis C virus infection in accelerating methylation process and affecting response to treatment in chronic hepatitis patients. This work aimed to elucidate the role of promoter methylation (PM) in response to antiviral therapy, and its contribution to the development of fibrosis through hepatocarcinogenesis-related genes. A total of 159 chronic hepatitis Egyptian patients versus 100 healthy control group were included. The methylation profile of a panel 9 genes (SFRP1, p14, p73, APC, DAPK, RASSF1A, LINE1, O6MGMT, and p16) was detected in patients’ plasma using methylation-specific polymerase chain reaction (MSP). Clinical and laboratory findings were gathered for patients with combined pegylated interferon and ribavirin antiviral therapy. Regarding the patients’ response to antiviral therapy, the percentage of non-responders for APC, O6MGMT, RASSF1A, SFRP1, and p16 methylated genes were significantly higher versus responders (P<0.05). Of the 159 included patients, the most frequent methylated genes were SFRP1 (102/159), followed by p16 (100/159), RASSF1A (98/159), then LINE1 (81/159), P73 (81/159), APC (78/159), DAPK (66/159), O6MGMT (66/159), and p14 (54/159). A total of 67/98 (68.4%) cases of RASSF1A methylated gene (P=0.0.024), and 62/100 (62%) cases of P16 methylated gene (P=0.03) were associated with mild-degree fibrosis. To recapitulate, the PM of SFRP1, APC, RASSF1A, O6MGMT, and p16 genes increases in chronic hepatitis C patients, and can affect patients’ response to antiviral therapy. The RASSF1A and P16 genes might have a role in the distinction between mild and marked fibrosis.

Citations

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  • The COVID-19 legacy: consequences for the human DNA methylome and therapeutic perspectives
    Carlo Gaetano, Sandra Atlante, Michela Gottardi Zamperla, Veronica Barbi, Davide Gentilini, Barbara Illi, Marco Malavolta, Fabio Martelli, Antonella Farsetti
    GeroScience.2024; 47(1): 483.     CrossRef
  • Variability of the HCV core region and host genetic and epigenetic factors can predict the response to pegylated interferon/ribavirin therapy in genotype 1b hepatitis C patients from Serbia
    Nikola Kokanov, Snezana Jovanovic-Cupic, Marina Siljic, Valentina Cirkovic, Nina Petrovic, Bojana Kozik, Milena Krajnovic
    Archives of Biological Sciences.2023; 75(3): 251.     CrossRef
  • RASSF1A and p16 promoter methylation and treatment response in chronic hepatitis C genotype 1b patients treated with pegylated interferon/ribavirin
    Nikola Kokanov, Milena Krajnovic, Snezana Cupic-Jovanovic, Bojana Kozik, Nina Petrovic, Ana Bozovic, Vesna Mandusic
    Archives of Biological Sciences.2022; 74(1): 57.     CrossRef
  • Screening, confirmation, and treatment rates of hepatitis C virus infection in a tertiary academic medical center in South Korea
    Jae Seung Lee, Hong Jun Choi, Hye Won Lee, Beom Kyung Kim, Jun Yong Park, Do Young Kim, Sang Hoon Ahn, Seung Up Kim
    Journal of Gastroenterology and Hepatology.2021; 36(9): 2479.     CrossRef
  • A longitudinal sampling study of transcriptomic and epigenetic profiles in patients with thrombocytopenia syndrome
    Yafen Wang, Shaoqing Han, Ruoxi Ran, Anling Li, Huanyu Liu, Mingjun Liu, Yongwei Duan, Xiong Zhang, Zhigang Zhao, Shihui Song, Xiaocheng Weng, Song-Mei Liu, Xiang Zhou
    Nature Communications.2021;[Epub]     CrossRef
  • 8,674 View
  • 144 Download
  • 5 Web of Science
  • Crossref

Viral hepatitis

Efficacy of L-carnitine on ribavirin-induced hemolytic anemia in patients with hepatitis C virus infection
Shinya Sato, Kei Moriya, Masanori Furukawa, Soichiro Saikawa, Tadashi Namisaki, Mitsuteru Kitade, Hideto Kawaratani, Kosuke Kaji, Hiroaki Takaya, Naotaka Shimozato, Yasuhiko Sawada, Kenichiro Seki, Koh Kitagawa, Takemi Akahane, Akira Mitoro, Yasushi Okura, Junichi Yamao, Hitoshi Yoshiji
Clin Mol Hepatol 2019;25(1):65-73.
Published online February 25, 2019
DOI: https://doi.org/10.3350/cmh.2018.0070
Background/Aims
L-carnitine not only alleviates hyperammonemia and reduces muscle cramps in patients with liver cirrhosis, but also improves anemia in patients with chronic hepatitis and renal dysfunction. This study prospectively evaluated the preventative efficacy of L-carnitine supplementation against hemolytic anemia during antiviral treatment using ribavirin in patients with hepatitis C virus (HCV)-related chronic liver disease.
Methods
A total of 41 patients with chronic hepatitis were consecutively enrolled in this study. Group A (n=22) received sofosbuvir plus ribavirin for 3 months, whereas group B (n=19) was treated with sofosbuvir, ribavirin, and L-carnitine. Hemoglobin concentration changes, the effects of antiviral treatment, and the health status of patients were analyzed using short form-8 questionnaires.
Results
A significantly smaller decrease in hemoglobin concentration was observed in group B compared to group A at every time point. Moreover, the prescribed dose intensity of ribavirin in group B was higher than that of group A, resulting in a higher ratio of sustained virological response (SVR) 24 in group B compared with group A. The physical function of patients in group B was also significantly improved compared to group A at the end of antiviral treatment.
Conclusions
L-carnitine supplementation alleviates ribavirin-induced hemolytic anemia in patients with HCV and helps relieve the physical burden of treatment with ribavirin-containing regimens. These advantages significantly increase the likelihood of achieving SVR.

Citations

Citations to this article as recorded by  Crossref logo
  • Altered branched chain ketoacids underlie shared metabolic phenotypes in type 1 diabetes and maple syrup urine disease
    Domenico Roberti, Abby L. Grier, Julie A. Reisz, Fara Vallefuoco, Alicia Key, Shaun Bevers, Monika Dzieciatkowska, Travis Nemkov, Marcella Contieri, Angela Zanfardino, Philip J. Norris, Michael P. Busch, Vienna Kauffman, Holmes D. Morton, Eric J. Earley,
    Communications Medicine.2025;[Epub]     CrossRef
  • Shining light on liquid–liquid phase separation in chronic liver disease
    Ming-Hui Li, Yang Yang, Qi-Qi Dong, Wen-Jie Sun, Hui Tao, Jing-Jing Yang
    Drug Discovery Today.2025; 30(10): 104464.     CrossRef
  • Advances in clinical application on nursing intervention for ribavirin-associated adverse events
    Li-Li Jiang, Qing Wang, Jia-Xin Zhang, Jing-Hui Fan, Jing Li
    Frontiers in Pharmacology.2025;[Epub]     CrossRef
  • LC–MS/MS separation and quantitation of ribavirin in chicken and comparison of different mass spectrometric platforms
    Daokun Xu, Haolun Huang, Wenyan Hu, Xinmei Liu, Jun Yang
    BMC Chemistry.2023;[Epub]     CrossRef
  • Can l-carnitine reduce post-COVID-19 fatigue?
    Roya Vaziri-harami, Parisa Delkash
    Annals of Medicine and Surgery.2022; 73: 103145.     CrossRef
  • Artemisinin and l‐carnitine combination therapy alters the erythrocytes redox status
    Mehdi Basaki, Akbar Hashemvand, Hossein Tayefi‐Nasrabadi, Yousef Panahi, Mahdi Dolatyarieslami
    Cell Biology International.2022; 46(7): 1137.     CrossRef
  • Hemolytic anemia in COVID-19
    Hayder M. Al-kuraishy, Ali I. Al-Gareeb, Ajeet Kaushik, Małgorzata Kujawska, Gaber El-Saber Batiha
    Annals of Hematology.2022; 101(9): 1887.     CrossRef
  • 11,651 View
  • 144 Download
  • 8 Web of Science
  • Crossref

Editorial

Viral hepatitis

Citations

Citations to this article as recorded by  Crossref logo
  • Real-Life Effectiveness and Safety of Glecaprevir/Pibrentasvir for Korean Patients with Chronic Hepatitis C at a Single Institution
    Young Joo Park, Hyun Young Woo, Jeong Heo, Sang Gyu Park, Young Mi Hong, Ki Tae Yoon, Dong Uk Kim, Gwang Ha Kim, Hyung Hoi Kim, Geun Am Song, Mong Cho
    Gut and Liver.2021; 15(3): 440.     CrossRef
  • Critical View on the Usage of Ribavirin in Already Existing Psychostimulant-Use Disorder
    Branka Petković, Srđan Kesić, Vesna Pešić
    Current Pharmaceutical Design.2020; 26(4): 466.     CrossRef
  • 9,156 View
  • 84 Download
  • 2 Web of Science
  • Crossref

Original Article

Viral hepatitis

Efficacy and safety of sofosbuvir plus ribavirin for Korean patients with hepatitis C virus genotype 2 infection: A retrospective multi-institutional study
Young Min Kim, Suk Bae Kim, Il Han Song, Sae Hwan Lee, Hong Soo Kim, Tae Hee Lee, Young Woo Kang, Seok Hyun Kim, Byung Seok Lee, Hee Bok Chae, Myeong Jun Song, Ji Woong Jang, Soon Young Ko, Jae Dong Lee
Clin Mol Hepatol 2018;24(3):311-318.
Published online June 4, 2018
DOI: https://doi.org/10.3350/cmh.2017.0070
Background/Aims
Sofosbuvir plus ribavirin is a standard treatment for patients infected with chronic hepatitis C virus (HCV) genotype 2 in Korea. The purpose of this study was to examine the efficacy and safety of this treatment in Korean patients with chronic HCV genotype 2 infection.
Methods
We retrospectively analyzed clinical data of patients treated with sofosbuvir plus ribavirin for chronic HCV genotype 2 from May 2016 to December 2017 at eight hospitals located in the Daejeon-Chungcheong area.
Results
A total of 172 patients were treated with sofosbuvir plus ribavirin. Of them, 163 patients completed the treatment, and 162 patients were tested for sustained virologic response 12 weeks after treatment discontinuation (SVR12). Mean age was 59.6±12.3 years (27–96), and 105 (64.4%) patients were female. Of the total patients, 49 (30.1%) were diagnosed with cirrhosis, and 31 of them were treated for 16 weeks. Sofosbuvir plus ribavirin was the first-line treatment for 144 (88.3%) patients. Eleven (6.7%) patients were intolerant to previous interferon-based treatment. Eight (5.0%) patients relapsed after interferon-based treatment. HCV RNA non-detection rate at 4, 8, and 12 weeks was 97.5%, 99.1%, and 99.3%, respectively, and SVR12 was 98.8% (161/163). During treatment, 18 (11.0%) patients had to reduce their administrated dose of ribavirin because of anemia. One patient stopped the treatment because of severe anemia. Other adverse events, including dizziness, indigestion, and headache, were found in 26 (16.0%) patients.
Conclusions
A 12-16 week treatment with sofosbuvir plus ribavirin is remarkably effective and well tolerated in Korean patients with chronic HCV genotype 2 infection.

Citations

Citations to this article as recorded by  Crossref logo
  • Combination treatment with sofosbuvir and ribavirin for patients diagnosed with hepatitis C genotype 2: A real-world, single-center study
    Ik Sung Choi, Kwang Min Kim, Sang Goon Shim
    Arab Journal of Gastroenterology.2021; 22(1): 23.     CrossRef
  • Real-Life Effectiveness and Safety of Glecaprevir/Pibrentasvir for Korean Patients with Chronic Hepatitis C at a Single Institution
    Young Joo Park, Hyun Young Woo, Jeong Heo, Sang Gyu Park, Young Mi Hong, Ki Tae Yoon, Dong Uk Kim, Gwang Ha Kim, Hyung Hoi Kim, Geun Am Song, Mong Cho
    Gut and Liver.2021; 15(3): 440.     CrossRef
  • Sofosbuvir‐based therapies in genotype 2 hepatitis C virus cirrhosis: A real‐life experience with focus on ribavirin dose
    Carlo Smirne, Antonio D'Avolio, Mattia Bellan, Alessandro Gualerzi, Maria G. Crobu, Mario Pirisi
    Pharmacology Research & Perspectives.2021;[Epub]     CrossRef
  • Novel variant in glycophorin c gene protects against ribavirin-induced anemia during chronic hepatitis C treatment
    Jennifer J. Lin, Catrina M. Loucks, Jessica N. Trueman, Britt I. Drögemöller, Galen E.B. Wright, Eric M. Yoshida, Jo-Ann Ford, Samuel S. Lee, Richard B. Kim, Bandar Al-Judaibi, Ute I. Schwarz, Alnoor Ramji, Edward Tam, Colin J. Ross, Bruce C. Carleton
    Biomedicine & Pharmacotherapy.2021; 143: 112195.     CrossRef
  • Incidence, risk factors and impact on virological response of anemia in chronic genotype 2 hepatitis C receiving sofosbuvir plus ribavirin
    Chi-Ching Chen, Shui-Yi Tung, Kuo-Liang Wei, Chien-Heng Shen, Te-Sheng Chang, Wei-Ming Chen, Huang-Wei Xu, Chih-Wei Yen, Yi-Hsing Chen, Sheng-Nan Lu, Chao-Hung Hung
    Journal of the Formosan Medical Association.2020; 119(1): 532.     CrossRef
  • Hepatocellular Carcinoma Risk According to Regimens for Eradication of Hepatitis C Virus; Interferon or Direct Acting Antivirals
    Hye Won Lee, Dai Hoon Han, Hye Jung Shin, Jae Seung Lee, Seung Up Kim, Jun Yong Park, Do Young Kim, Sang Hoon Ahn, Beom Kyung Kim
    Cancers.2020; 12(11): 3414.     CrossRef
  • Real-Life Effectiveness and Safety of Sofosbuvir-Based Therapy in Genotype 2 Chronic Hepatitis C Patients in South Korea, with Emphasis on the Ribavirin Dose
    Eun Sun Jang, Kyung-Ah Kim, Young Seok Kim, In Hee Kim, Byung Seok Lee, Youn Jae Lee, Woo Jin Chung, Sook-Hyang Jeong
    Gut and Liver.2020; 14(6): 775.     CrossRef
  • Direct-acting antivirals in East Asian hepatitis C patients: real-world experience from the REAL-C Consortium
    Chung-Feng Huang, Etsuko Iio, Dae Won Jun, Eiichi Ogawa, Hidenori Toyoda, Yao-Chun Hsu, Hiroaki Haga, Shinji Iwane, Masaru Enomoto, Dong Hyun Lee, Grace Wong, Chen-Hua Liu, Toshifumi Tada, Wan-Long Chuang, Ramsey Cheung, Jun Hayashi, Cheng-Hao Tseng, Sato
    Hepatology International.2019; 13(5): 587.     CrossRef
  • Comparison of the Clinical Characteristics and Outcomes between Leprosy-Affected Persons in Sorokdo and the General Population Affected by Chronic Hepatitis C in Korea
    Young-Hwan Ahn, Hyungcheol Park, Myeon Jae Lee, Dong Hyun Kim, Sung Bum Cho, Eunae Cho, Chung Hwan Jun, Sung Kyu Choi
    Gut and Liver.2019; 13(5): 549.     CrossRef
  • Does the old-fashioned sofosbuvir plus ribavirin treatment in genotype 2 chronic hepatitis C patients still works for Koreans?
    Jong Eun Yeon
    Clinical and Molecular Hepatology.2018; 24(3): 294.     CrossRef
  • Ribavirin/sofosbuvir

    Reactions Weekly.2018; 1727(1): 247.     CrossRef
  • 10,636 View
  • 206 Download
  • 11 Web of Science
  • Crossref

Case Report

Viral hepatitis

Regression of esophageal varices and splenomegaly in two patients with hepatitis-C-related liver cirrhosis after interferon and ribavirin combination therapy
Soon Jae Lee, Yoo-Kyung Cho, Soo-Young Na, Eun Kwang Choi, Sun Jin Boo, Seung Uk Jeong, Hyung Joo Song, Heung Up Kim, Bong Soo Kim, Byung-Cheol Song
Clin Mol Hepatol 2016;22(3):390-395.
Published online August 30, 2016
DOI: https://doi.org/10.3350/cmh.2015.0050
Some recent studies have found regression of liver cirrhosis after antiviral therapy in patients with hepatitis C virus (HCV)-related liver cirrhosis, but there have been no reports of complete regression of esophageal varices after interferon/ peg-interferon and ribavirin combination therapy. We describe two cases of complete regression of esophageal varices and splenomegaly after interferon-alpha and ribavirin combination therapy in patients with HCV-related liver cirrhosis. Esophageal varices and splenomegaly regressed after 3 and 8 years of sustained virologic responses in cases 1 and 2, respectively. To our knowledge, this is the first study demonstrating that complications of liver cirrhosis, such as esophageal varices and splenomegaly, can regress after antiviral therapy in patients with HCV-related liver cirrhosis.

Citations

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  • Long term changes in thrombocytopenia and leucopenia after HCV eradication with direct-acting antivirals
    Kazuto Tajiri, Kazuhiko Okada, Hiroyuki Ito, Kengo Kawai, Yoshiro Kashii, Yoshiharu Tokimitsu, Nozomu Muraishi, Aiko Murayama, Yuka Hayashi, Masami Minemura, Terumi Takahara, Yukihiro Shimizu, Ichiro Yasuda
    BMC Gastroenterology.2023;[Epub]     CrossRef
  • Small Esophageal Varices in Patients with Cirrhosis—Should We Treat Them?
    Thomas Reiberger, Theresa Bucsics, Rafael Paternostro, Nikolaus Pfisterer, Florian Riedl, Mattias Mandorfer
    Current Hepatology Reports.2018; 17(4): 301.     CrossRef
  • 14,500 View
  • 134 Download
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Original Article

Viral hepatitis

Highly effective peginterferon α-2a plus ribavirin combination therapy for chronic hepatitis C in hemophilia in Korea
Suh Yoon Yang, Hyun Woong Lee, Youn Jae Lee, Sung Jae Park, Ki Young Yoo, Hyung Joon Kim
Clin Mol Hepatol 2015;21(2):125-130.
Published online June 26, 2015
DOI: https://doi.org/10.3350/cmh.2015.21.2.125
Background/Aims

Chronic hepatitis C (CHC) is a major comorbidity in patients with hemophilia. However, there are no published data on the efficacy of antiviral therapy in Korea. We assessed the safety and efficacy of combination therapy with peginterferon α-2a plus ribavirin for CHC in hemophilia.

Methods

Patients (n=115) were enrolled between March 2007 and December 2008. Seventy-seven patients were genotype 1 or 6, and 38 patients were genotype 2 or 3. We evaluated rapid virologic responses (RVRs), early virologic response (EVRs), end-of-treatment response (ETRs), sustained virologic response (SVRs), and relapses. Safety evaluations included adverse events and laboratory tests.

Results

Eleven patients were excluded from the study because they had been treated previously. Among the remaining 104 treatment-naïve patients, RVR was achieved in 64 (60.6%), ETR was achieved in 95 (91.3%), and SVR was achieved in 89 (85.6%). Relapse occurred in eight patients (8.9%). Common adverse events were hair loss (56.7%) and headache (51.0%). Common hematologic adverse events were neutropenia (22.1%), anemia (27.9%), and thrombocytopenia (3.8%). However, there were no serious adverse events such as bleeding. RVR was the only predictor of SVR in multivariate analysis.

Conclusions

Peginterferon α-2a plus ribavirin combination treatment produced a favorable response rate in CHC patients with hemophilia without serious adverse events.

Citations

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  • Low Incidence of Hepatocellular Carcinoma after Antiviral Therapy in Patients with Chronic Hepatitis C and Hemophilia
    In Jung Kim, Sung Hwan Yoo, Sora Kim, Young Youn Cho, Ki Young Yoo, Hyung Joon Kim, Hyun Woong Lee
    Journal of Clinical Medicine.2022; 11(5): 1451.     CrossRef
  • Viral hepatitis in haemophilia: historical perspective and current management
    Cas J. Isfordink, Karel J. van Erpecum, Marc van der Valk, Evelien P. Mauser‐Bunschoten, Michael Makris
    British Journal of Haematology.2021; 195(2): 174.     CrossRef
  • Direct Acting Antiviral Agents in Korean Patients with Chronic Hepatitis C and Hemophilia Who Are Treatment-Naïve or Treatment-Experienced
    Hyun Woong Lee, Ki Young Yoo, Joung Won Won, Hyung Joon Kim
    Gut and Liver.2017; 11(5): 721.     CrossRef
  • KASL clinical practice guidelines: management of hepatitis C

    Clinical and Molecular Hepatology.2016; 22(1): 76.     CrossRef
  • 12,406 View
  • 72 Download
  • 4 Web of Science
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Editorial

Viral hepatitis

Hepatitis C virus infection in patients with hemophilia in Korea: Is antiviral therapy effective and safe?
Woo Sun Rou, Byung Seok Lee
Clin Mol Hepatol 2015;21(2):122-124.
Published online June 26, 2015
DOI: https://doi.org/10.3350/cmh.2015.21.2.122
  • 10,460 View
  • 107 Download
  • 2 Web of Science

Original Article

Viral hepatitis

High effectiveness of peginterferon alfa-2a plus ribavirin therapy in Korean patients with chronic hepatitis C in clinical practice
Nae-Yun Heo, Young-Suk Lim, Han Chu Lee, Yung Sang Lee, Kang Mo Kim, Kwan Soo Byun, Kwang-Hyub Han, Kwan Sik Lee, Seung Woon Paik, Seung Kew Yoon, Dong Jin Suh
Korean J Hepatol 2013;19(1):60-69.
Published online March 25, 2013
DOI: https://doi.org/10.3350/cmh.2013.19.1.60
Background/Aims

Identifying the impact of a patient's ethnicity on treatment responses in clinical practice may assist in providing individualized treatment regimens for chronic hepatitis C (CHC). The effectiveness of standard peginterferon plus ribavirin therapy and the need for triple combination therapy with protease inhibitors in Koreans remain matters of debate. These issues were investigated in the present study.

Methods

The clinical data of 272 treatment-naïve Korean CHC patients who were treated in a community-based clinical trial (Clinical Trial group; n=51) and in clinical practice (Cohort group; n=221), were analyzed and compared. All were treated with standard protocols of peginterferon alfa-2a plus ribavirin therapy.

Results

For patients with hepatitis C virus (HCV) genotype 1, the sustained virological response (SVR) rates in the Clinical Trial and Cohort groups were 81% (21/26) and 55% (58/106), respectively, by intention-to-treat (ITT) analysis (P=0.02), and 100% (13/13) and 80% (32/40), respectively, in treatment-adherent patients (P=0.18). For patients with HCV genotype 2, the SVR rates in these two groups were 96% (24/25) and 88% (101/115), respectively, by ITT analysis (P=0.31). Adherence and treatment duration were independent predictors of SVR for genotypes 1 and 2, respectively (P<0.01 for each). Korean patients with CHC achieved high SVR rates with peginterferon alfa-2a plus ribavirin in both the clinical trial and clinical practice settings.

Conclusions

Measures to raise adherence to standard therapy in clinical practice may improve the SVR rates in these patients as effectively as adding protease inhibitors, thus obviating the need for the latter.

Citations

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  • Association between Anti-Hepatitis C Viral Intervention Therapy and Risk of Sjögren’s Syndrome: A National Retrospective Analysis
    Chien-Hsueh Tung, Yen-Chun Chen, Yi-Chun Chen
    Journal of Clinical Medicine.2022; 11(15): 4259.     CrossRef
  • Platelet count is associated with sustained virological response rates in treatments for chronic hepatitis C
    Baek Gyu Jun, Eui Ju Park, Woong Cheul Lee, Jae Young Jang, Soung Won Jeong, Young Don Kim, Gab Jin Cheon, Young Sin Cho, Sae Hwan Lee, Hong Soo Kim, Yun Nah Lee, Sang Gyune Kim, Young Seok Kim, Boo Sung Kim
    The Korean Journal of Internal Medicine.2019; 34(5): 989.     CrossRef
  • The Efficacy and Safety of Direct-acting Antiviral Treatment for Chronic Hepatitis C Patients: A Single Center Study
    Seong Jun Park, Ah Ran Kim, Won Hyeok Choe, Jeong Han Kim, Byung Chul Yoo, So Young Kwon
    The Korean Journal of Gastroenterology.2018; 72(4): 197.     CrossRef
  • Treatment Response and Long-Term Outcome of Peginterferon α and Ribavirin Therapy in Korean Patients with Chronic Hepatitis C
    Chang Ho Jung, Soon Ho Um, Tae Hyung Kim, Sun Young Yim, Sang Jun Suh, Hyung Joon Yim, Yeon Seok Seo, Hyuk Soon Choi, Hoon Jai Chun
    Gut and Liver.2016; 10(5): 808.     CrossRef
  • No association between the IL28B SNP and response to peginterferon plus ribavirin combination treatment in Korean chronic hepatitis C patients
    Nae-Yun Heo, Young-Suk Lim, Woochang Lee, Minkyung Oh, Jiyun An, Danbi Lee, Ju Hyun Shim, Kang Mo Kim, Han Chu Lee, Yung Sang Lee, Dong Jin Suh
    Clinical and Molecular Hepatology.2014; 20(2): 177.     CrossRef
  • Naturally Occurring Mutations in the Nonstructural Region 5B of Hepatitis C Virus (HCV) from Treatment-Naïve Korean Patients Chronically Infected with HCV Genotype 1b
    Dong-Won Kim, Seoung-Ae Lee, Hong Kim, You-Sub Won, Bum-Joon Kim, Jason Blackard
    PLoS ONE.2014; 9(1): e87773.     CrossRef
  • Is peginterferon and ribavirin therapy effective in Korean patients with chronic hepatitis C?
    Young Kul Jung, Ju Hyun Kim
    Clinical and Molecular Hepatology.2013; 19(1): 26.     CrossRef
  • 11,263 View
  • 62 Download
  • 6 Web of Science
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Editorial

Viral hepatitis

Is peginterferon and ribavirin therapy effective in Korean patients with chronic hepatitis C?
Young Kul Jung, Ju Hyun Kim
Korean J Hepatol 2013;19(1):26-28.
Published online March 25, 2013
DOI: https://doi.org/10.3350/cmh.2013.19.1.26

Citations

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  • Immunological dynamics associated with rapid virological response during the early phase of type I interferon therapy in patients with chronic hepatitis C
    Jae-Won Lee, Won Kim, Eun-Kyung Kwon, Yuri Kim, Hyun Mu Shin, Dong-Hyun Kim, Chan-Ki Min, Ji-Yeob Choi, Won-Woo Lee, Myung-Sik Choi, Byeong Gwan Kim, Nam-Hyuk Cho, Eui-Cheol Shin
    PLOS ONE.2017; 12(6): e0179094.     CrossRef
  • Final Report of Unmet Needs of Interferon-Based Therapy for Chronic Hepatitis C in Korea: Basis for Moving into the Direct-Acting Antiviral Era
    Eun Sun Jang, Young Seok Kim, Kyung-Ah Kim, Youn Jae Lee, Woo Jin Chung, In Hee Kim, Byung Seok Lee, Sook-Hyang Jeong
    Gut and Liver.2017; 11(4): 543.     CrossRef
  • Phylogeny and molecular evolution of the hepatitis C virus
    Paulina Jackowiak, Karolina Kuls, Lucyna Budzko, Anna Mania, Magdalena Figlerowicz, Marek Figlerowicz
    Infection, Genetics and Evolution.2014; 21: 67.     CrossRef
  • No association between the IL28B SNP and response to peginterferon plus ribavirin combination treatment in Korean chronic hepatitis C patients
    Nae-Yun Heo, Young-Suk Lim, Woochang Lee, Minkyung Oh, Jiyun An, Danbi Lee, Ju Hyun Shim, Kang Mo Kim, Han Chu Lee, Yung Sang Lee, Dong Jin Suh
    Clinical and Molecular Hepatology.2014; 20(2): 177.     CrossRef
  • 8,925 View
  • 53 Download
  • Crossref

Original Articles

Viral hepatitis

Efficacy of peginterferon and ribavirin is associated with the IL28B gene in Korean patients with chronic hepatitis C
Seok Hoo Jeong, Young Kul Jung, Jae Won Yang, Sang Jin Park, Jong Woo Kim, Oh Sang Kwon, Yun Soo Kim, Duck Joo Choi, Ju Hyun Kim
Korean J Hepatol 2012;18(4):360-367.
Published online December 21, 2012
DOI: https://doi.org/10.3350/cmh.2012.18.4.360
Background/Aims

Sustained virologic response (SVR) for the treatment of chronic hepatitis C (CHC) may differ with ethnicity due to differences in genetic traits. This study evaluated the efficacy of peginterferon and ribavirin, and the association between IL28B genotypes and the treatment efficacy in Korean CHC patients.

Methods

This was a retrospective cohort study using data from medical records. Eighty-five CHC patients were eligible for assessment of the efficacy of antiviral therapy, and 47 patients were available for an IL28B genetic study, which was performed using the Multiplex tetra-primer PCR method for rs12979860.

Results

Overall, the early virologic response rate was 87.1%: 84.9% in HCV genotype 1 and 90.6% in genotype 2. The overall end-of-treatment virologic response rate was 81.2%: 75.5% in genotype 1 and 90.6% in genotype 2. The overall SVR rate was 81.2%: 75.5% in genotype 1 and 90.6% in genotype 2. For rs12979860, the frequencies of polymorphisms were 89% for the CC type, 11% for the CT type, and 0% for the TT type. Their overall SVR rate was 87% (39/47): 90.5% (38/42) for the CC type and 20% (1/5) for the CT type. For genotype 1, SVR rates were 88% (21/24) for the CC type and 0% (0/4) for the CT type. Multivariate analysis revealed that the IL28B-CC type was a good predictor for SVR.

Conclusions

The SVR of the combination therapy in Koreans was higher than that observed in Western countries. This finding might be attributable to the high prevalence of IL28B-CC type among Koreans, which may be a good predictor of SVR.

Citations

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  • Uncovering the immune microenvironment and molecular subtypes of hepatitis B-related liver cirrhosis and developing stable a diagnostic differential model by machine learning and artificial neural networks
    Shengke Zhang, Chenglu Jiang, Lai Jiang, Haiqing Chen, Jinbang Huang, Jieying Zhang, Rui Wang, Hao Chi, Guanhu Yang, Gang Tian
    Frontiers in Molecular Biosciences.2023;[Epub]     CrossRef
  • Genetic screening to avoid adverse drug reactions from medication use and approach patients' better outcomes: A lesson learn from the report of the Queen Savang Vadhana Memorial Hospital
    Kessada Tunwongsa, Malinee Chonnawakul, Nopavut Geratikornsupuk, Karunrat Tewthanom
    Health Science Reports.2022;[Epub]     CrossRef
  • The change in the nationwide seroprevalence of hepatitis C virus and the status of linkage to care in South Korea from 2009 to 2015
    Eun Sun Jang, Moran Ki, Hwa Young Choi, Kyung-Ah Kim, Sook-Hyang Jeong
    Hepatology International.2019; 13(5): 599.     CrossRef
  • Final Report of Unmet Needs of Interferon-Based Therapy for Chronic Hepatitis C in Korea: Basis for Moving into the Direct-Acting Antiviral Era
    Eun Sun Jang, Young Seok Kim, Kyung-Ah Kim, Youn Jae Lee, Woo Jin Chung, In Hee Kim, Byung Seok Lee, Sook-Hyang Jeong
    Gut and Liver.2017; 11(4): 543.     CrossRef
  • Real-life prevalence of resistance-associated variants against non-structural protein 5A inhibitors and efficiency of Daclatasvir + Asunaprevir therapy in Korean patients with genotype 1b hepatitis C
    Jung Hwan Yu, Jung Il Lee, Kwan Sik Lee, Ja Kyung Kim
    Virology Journal.2017;[Epub]     CrossRef
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    Clinical and Molecular Hepatology.2016; 22(1): 76.     CrossRef
  • Incidence and risk factors of hepatitis C virus infection among human immunodeficiency virus (HIV) patients in a large HIV clinic in South Korea
    Shinwon Lee, Sun Hee Lee, Su Jin Lee, Kye-Hyung Kim, Jeong Eun Lee, Heerim Cho, Seung Geun Lee, Joo Seop Chung, Ihm Soo Kwak
    The Korean Journal of Internal Medicine.2016; 31(4): 772.     CrossRef
  • Lower Incidence of Hepatocellular Carcinoma and Cirrhosis in Hepatitis C Patients with Sustained Virological Response by Pegylated Interferon and Ribavirin
    Chansoo Moon, Kyu Sik Jung, Do Young Kim, Oidov Baatarkhuu, Jun Yong Park, Beom Kyung Kim, Seung Up Kim, Sang Hoon Ahn, Kwang-Hyub Han
    Digestive Diseases and Sciences.2015; 60(2): 573.     CrossRef
  • IFN-λ gene polymorphisms as predictive factors in chronic hepatitis C treatment-naive patients without access to protease inhibitors
    Daniele Blasquez Olmedo, Samária Ali Cader, Luís Cristóvão Porto
    Journal of Medical Virology.2015; 87(10): 1702.     CrossRef
  • No association between the IL28B SNP and response to peginterferon plus ribavirin combination treatment in Korean chronic hepatitis C patients
    Nae-Yun Heo, Young-Suk Lim, Woochang Lee, Minkyung Oh, Jiyun An, Danbi Lee, Ju Hyun Shim, Kang Mo Kim, Han Chu Lee, Yung Sang Lee, Dong Jin Suh
    Clinical and Molecular Hepatology.2014; 20(2): 177.     CrossRef
  • KASL clinical practice guidelines: Management of Hepatitis C

    Clinical and Molecular Hepatology.2014; 20(2): 89.     CrossRef
  • Is peginterferon and ribavirin therapy effective in Korean patients with chronic hepatitis C?
    Young Kul Jung, Ju Hyun Kim
    Clinical and Molecular Hepatology.2013; 19(1): 26.     CrossRef
  • The Impact of Inosine Triphosphatase Variants on Hemoglobin Level and Sustained Virologic Response of Chronic Hepatitis C in Korean
    Ju Seung Kim, Sung-Min Ahn, Young Kul Jung, Oh Sang Kwon, Yun Soo Kim, Duck Joo Choi, Ju Hyun Kim
    Journal of Korean Medical Science.2013; 28(8): 1213.     CrossRef
  • 10,044 View
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Viral hepatitis

A reduced dose of ribavirin does not influence the virologic response during pegylated interferon alpha-2b and ribavirin combination therapy in patients with genotype 1 chronic hepatitis C
Byung Chul You, Young Seok Kim, Hun il Kim, Se Hun Kim, Seung Sik Park, Yu Ri Seo, Sang Gyune Kim, Se Whan Lee, Hong Soo Kim, Soung Won Jeong, Jae Young Jang, Boo Sung Kim
Korean J Hepatol 2012;18(3):272-278.
Published online September 25, 2012
DOI: https://doi.org/10.3350/cmh.2012.18.3.272
Background/Aims

When combined with pegylated interferon alpha-2b (Peg-IFN α-2b) for the treatment of genotype 1 chronic hepatitis C (CHC) in Korea, the current guideline for the initial ribavirin (RBV) dose is based on body weight. However, since the mean body weight is lower for Korean patients than for patients in Western countries, current guidelines might result in Korean patients being overdosed with RBV.

Methods

We retrospectively reviewed the medical records of patients with genotype 1 CHC who were treated with Peg-IFN α-2b and RBV combination therapy. We divided the patients into groups A (≥15 mg/kg/day, n=23) and B (<15 mg/kg/day, n=26), given that the standard dose is 15 mg/kg/day. The clinical course in terms of the virologic response, adverse events, and dose modification rate was compared between the two groups after therapy completion.

Results

The early response rates (92.0% vs. 83.3%, P=0.634) and sustained virologic response rates (82.6% vs. 73.1%, P=0.506) did not differ significantly between the two groups. During the treatment period, the RBV dose reduction rate was significantly higher in group A than in group B (60.9% vs. 23.1%, P=0.01).

Conclusions

RBV dose reduction is performed frequently when patients are treated according to the current Korean guidelines. Given that lowering the RBV dose did not appear to decrease the virologic response during therapy, reducing RBV doses below the current Korean guideline may be effective for treatment, especially in low-weight patients.

Citations

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  • The Impact of Inosine Triphosphatase Variants on Hemoglobin Level and Sustained Virologic Response of Chronic Hepatitis C in Korean
    Ju Seung Kim, Sung-Min Ahn, Young Kul Jung, Oh Sang Kwon, Yun Soo Kim, Duck Joo Choi, Ju Hyun Kim
    Journal of Korean Medical Science.2013; 28(8): 1213.     CrossRef
  • 9,667 View
  • 44 Download
  • Crossref

Editorial

Viral hepatitis

Impact of ribavirin dose reduction during treatment in chronic hepatitis C genotype 1 patients
Woo Jin Chung
Korean J Hepatol 2012;18(3):268-271.
Published online September 25, 2012
DOI: https://doi.org/10.3350/cmh.2012.18.3.268

Citations

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  • Adverse drug reactions during hepatitis C treatment with direct-acting antivirals: The role of medication errors, their impact on treatment discontinuation and their preventability. New insights from the Campania Region (Italy) spontaneous reporting syste
    Maurizio Sessa, Francesca Futura Bernardi, Andrea Vitale, Beniamino Schiavone, Giulia Gritti, Annamaria Mascolo, Michele Bertini, Cristina Scavone, Liberata Sportiello, Francesco Rossi, Annalisa Capuano
    Journal of Clinical Pharmacy and Therapeutics.2018; 43(6): 867.     CrossRef
  • 7,889 View
  • 53 Download
  • Crossref

Original Article

Rapid normalization of alanine aminotransferase predicts viral response during combined peginterferon and ribavirin treatment in chronic hepatitis C patients
Yun Jung Kim, Byoung Kuk Jang, Eun Soo Kim, Kyung Sik Park, Kwang Bum Cho, Woo Jin Chung, Jae Seok Hwang
Korean J Hepatol 2012;18(1):41-47.
Published online March 22, 2012
DOI: https://doi.org/10.3350/kjhep.2012.18.1.41
Background/Aims

The treatment for chronic hepatitis C (CHC) is removal of the virus in order to prevent progression to liver cirrhosis and hepatocellular carcinoma (HCC). Few data have been presented regarding the clinical significance of changes in the alanine aminotransferase (ALT) level in this context. We analyzed the patterns of changes in ALT level and investigated the relationship between the rapid normalization of ALT and sustained virologic response (SVR) after combined treatment with peginterferon and ribavirin.

Methods

CHC patients (n=370) were classified into four groups according to the initial ALT level and subsequent changes: (1) initially abnormal ALT level and sustained abnormal ALT level during treatment, (2) initially abnormal ALT level but achievement of ALT normalization, (3) initially normal ALT level and variable ALT abnormality during treatment, and (4) initially normal ALT level and sustained normalization of ALT level during treatment. We subdivided groups 1 and 2 into those with patterns of decreased and normalization of ALT, with or without rapid normalization. We checked the end-treatment response (ETR) and SVR rates in each group and the factors associated with SVR, including patterns of changes in ALT level.

Results

A total of 168 patients completed the therapy (age=54.34±10.64 years [mean±SD], 95 males [56.5%], genotype 1:82 [48.8%]). SVR was achieved in 115 (68.45%) of the completely treated patients. The SVR rate was significantly lower in group 1 than in group 2 (37.8 vs. 81.6%, P<0.001), and significantly higher in the rapid normalization group than in the group without rapid normalization (78.5% vs. 41.2%, P<0.001). Multiple logistic regression analysis revealed that age (odds ratio [OR]=0.94, 95% confidence interval [CI]=0.91-0.98, P=0.005), viral genotype (OR=2.76, 95% CI=1.20-6.38, P=0.017), and initial hepatitis C virus RNA titer (OR=0.28, 95% CI=0.10-0.75, P=0.012) were identified as independent significant predictive factors for SVR.

Conclusions

The SVR rate is significantly associated with normalization, and especially rapid normalization of ALT. Rapid normalization of ALT by 4 weeks after treatment might be a useful response factor that is readily available in clinical practice, and especially for genotype 1 patients.

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    Miriam Watafua, Jane I. Ejiofor, Jamilu Ya’u, Aminu Musa, Mubarak Hussaini Ahmad
    Toxicology and Environmental Health Sciences.2025;[Epub]     CrossRef
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    Hyunwoo Oh, Chan Hyuk Park, Dae Won Jun
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    Dalia El Sabaawy, Sahar El-Haggar, Hoda El-Bahrawy, Imam Waked, Hala El-Said
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  • Advanced Hepatic Fibrosis and Steatosis Are Associated With Persistent Alanine Aminotransferase Elevation in Chronic Hepatitis C Patients Negative for Hepatitis C Virus RNA During Pegylated Interferon Plus Ribavirin Therapy
    C.-C. Liang, C.-H. Liu, C.-S. Chung, C.-K. Lin, T.-H. Su, H.-C. Yang, C.-J. Liu, P.-J. Chen, D.-S. Chen, J.-H. Kao
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    Luís Henrique Bezerra Cavalcanti Sette, Edmundo Pessoa de Almeida Lopes
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    Hany Shehab, Tamer Elbaz, Dalia Deraz, Amal Hafez, Inas Elattar
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    Chih-Wei Tseng, Chi-Yi Chen, Ting-Tsung Chang, Shinn-Jia Tzeng, Yu-Hsi Hsieh, Tsung-Hsing Hung, Ching-Chih Lee, Shu-Fen Wu, Kuo-Chih Tseng, Ming-Lung Yu
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    Luís Henrique Bezerra Cavalcanti Sette, Edmundo Pessoa de Almeida Lopes
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    Tae Yeob Kim
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Review

Recent trends in the treatment of chronic hepatitis C
Dae Won Jun, Won Young Tak, Si Hyun Bae, Youn Jae Lee
Korean J Hepatol 2012;18(1):22-28.
Published online March 22, 2012
DOI: https://doi.org/10.3350/kjhep.2012.18.1.22

Pegylated interferon and ribavirin combination therapy is accepted as the standard antiviral treatment for chronic hepatitis C regardless of HCV genotype. This combination therapy achieves higher response rates than previous therapy, but, nevertheless, a large proportion of patients suffer from treatment failure or adverse events. Recent clinical studies of viral kinetics during antiviral treatment have led to the introduction of response-guided therapy, the concept of 'customized therapy depending on viral response', which focuses on modulation of the treatment period depending on the viral response to create a sustained viral response without unnecessary medication and costs. New upcoming direct-acting antivirals (DAAs) maximize response rate, and triple therapy including DAAs along with pegylated interferon and ribavirin combination therapy could soon be the standard therapy. In this article, we reviewed the factors affecting treatment, response guided treatment, retreatment after failure of standard treatment, management of adverse events during treatment, and new treatment options.

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  • HCV Infection: An Enigma, Recent Advances and New Paradigms for its Treatment
    Waleed Hassan AlMalki
    Future Virology.2013; 8(4): 381.     CrossRef
  • Protease Inhibitors for Hepatitis C: Economic Implications
    Stuart J. Turner, Jack Brown, Joseph A. Paladino
    PharmacoEconomics.2013; 31(9): 739.     CrossRef
  • 13,234 View
  • 68 Download
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Original Articles

Peginterferon alpha and ribavirin combination therapy in patients with hepatitis C virus-related liver cirrhosis
Kyung Hoon Kim, Byoung Kuk Jang, Woo Jin Chung, Jae Seok Hwang, Young Oh Kweon, Won Young Tak, Heon Ju Lee, Chang Hyeong Lee, Jeong Ill Suh
Korean J Hepatol 2011;17(3):220-225.
Published online September 30, 2011
DOI: https://doi.org/10.3350/kjhep.2011.17.3.220
Background/Aims

Pegylated interferon (peginterferon) and ribavirin combination therapy is less effective and associated with a higher frequency of serious complications in chronic hepatitis C patients with cirrhosis than in noncirrhotic patients. This study evaluated the efficacy and tolerability of peginterferon and ribavirin treatment in patients with hepatitis C virus (HCV)-related cirrhosis.

Methods

Eighty-six patients with clinically diagnosed liver cirrhosis were treated with either peginterferon alpha-2a (n=51) or peginterferon alpha-2b (n=35) plus ribavirin. The sustained virologic response (SVR) and adverse effects were analyzed retrospectively.

Results

Of the 86 patients (55 males), 48 patients (55.8%) had HCV genotype 1 infection and 38 (44.2%) had genotype non-1 infection. The overall SVR rate was 34.9% (30/86), and the rates of SVR in the genotype 1 and non-1 patients were 20.8% (10/48) and 52.6% (20/38), respectively. The multivariate analysis revealed that having HCV genotype 1 (P=0.003) and high baseline viral load (>8.0×105 IU/mL, P=0.012) were the independent predictive factors for SVR failure. In 20.9% (18/86) of the patients, treatment was not completed due to adverse events (27.8%), loss to follow-up (50.0%), and other reasons (22.2%).

Conclusions

Peginterferon and ribavirin combination therapy was relatively effective and feasible for clinically diagnosed HCV patients, especially in those with genotype non-1 infection and low baseline viral load.

Citations

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  • Cost‐effectiveness of sofosbuvir plus ribavirin therapy for hepatitis C virus genotype 2 infection in South Korea
    Wankyo Chung, Kyung‐Ah Kim, Eun Sun Jang, Moran Ki, Hwa Young Choi, Sook‐Hyang Jeong
    Journal of Gastroenterology and Hepatology.2019; 34(4): 776.     CrossRef
  • Association of Toll-Like Receptor 3 Single-Nucleotide Polymorphisms and Hepatitis C Virus Infection
    Mashael R. Al-Anazi, Sabine Matou-Nasri, Ayman A. Abdo, Faisal M. Sanai, Saad Alkahtani, Saud Alarifi, Abdullah A. Alkahtane, Hamad Al-Yahya, Daoud Ali, Mohammed S. Alessia, Bushra Alshahrani, Mohammed N. Al-Ahdal, Ahmed A. Al-Qahtani
    Journal of Immunology Research.2017; 2017: 1.     CrossRef
  • Urgency to treat patients with chronic hepatitis C in Asia
    Jia‐Horng Kao, Sang Hoon Ahn, Rong‐Nan Chien, Mong Cho, Wan‐Long Chuang, Sook‐Hyang Jeong, Chen‐Hua Liu, Seung‐Woon Paik
    Journal of Gastroenterology and Hepatology.2017; 32(5): 966.     CrossRef
  • The influence of host factors and sequence variability of the p7 region on the response to pegylated interferon/ribavirin therapy for chronic hepatitis C genotype 1b in patients from Serbia
    Snezana Jovanovic-Cupic, Sanja Glisic, Maja Stanojevic, Darko Nozic, Nina Petrovic, Vesna Mandusic, Milena Krajnovic
    Archives of Virology.2016; 161(5): 1189.     CrossRef
  • Treatment Response and Long-Term Outcome of Peginterferon α and Ribavirin Therapy in Korean Patients with Chronic Hepatitis C
    Chang Ho Jung, Soon Ho Um, Tae Hyung Kim, Sun Young Yim, Sang Jun Suh, Hyung Joon Yim, Yeon Seok Seo, Hyuk Soon Choi, Hoon Jai Chun
    Gut and Liver.2016; 10(5): 808.     CrossRef
  • All‐oral daclatasvir plus asunaprevir for chronic hepatitis C virus (HCV) genotype 1b infection: a sub‐analysis in Asian patients from the HALLMARK DUAL study
    Jia‐Horng Kao, Youn‐Jae Lee, Jeong Heo, Sang‐Hoon Ahn, Young‐Suk Lim, Cheng‐Yuan Peng, Ting‐Tsung Chang, Anne Torbeyns, Eric Hughes, Rafia Bhore, Stephanie Noviello
    Liver International.2016; 36(10): 1433.     CrossRef
  • Treatment of Hepatitis C in Special Conditions: Liver Cirrhosis
    Geum-Youn Gwak
    Korean Journal of Medicine.2015; 88(6): 643.     CrossRef
  • Management of HCV in Cirrhosis—a Rapidly Evolving Landscape
    Suraj A. Sharma, Jordan J. Feld
    Current Gastroenterology Reports.2015;[Epub]     CrossRef
  • KASL clinical practice guidelines: Management of Hepatitis C

    Clinical and Molecular Hepatology.2014; 20(2): 89.     CrossRef
  • Advanced fibrosis is not a negative pretreatment predictive factor for genotype 2 or 3 chronic hepatitis C patients
    Hyun Seok Lee, Young Oh Kweon, Won Young Tak, Soo Young Park, Eun Jung Kang, Yu Lim Lee, Hae Min Yang, Hyun Woo Park
    Clinical and Molecular Hepatology.2013; 19(2): 148.     CrossRef
  • Severe adverse events during antiviral therapy in hepatitis C virus cirrhotic patients: A systematic review
    Simona Bota
    World Journal of Hepatology.2013; 5(3): 120.     CrossRef
  • 9,872 View
  • 57 Download
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Durability of a sustained virological response in chronic hepatitis C patients treated with pegylated interferon alfa and ribavirin
Sang Bun Choi, Youn Jae Lee, Jae Ik Lee, Young Jin Song, Byoung Jin Choi, Jong Han Kim, Eun Uk Jung, Sung Jae Park, Sang Heon Lee, Ji Hyun Kim, Jung Sik Choi, Sam Ryong Jee, Sang Yong Seol
Korean J Hepatol 2011;17(3):183-188.
Published online September 30, 2011
DOI: https://doi.org/10.3350/kjhep.2011.17.3.183
Background/Aims

The reappearance rates of hepatitis C virus (HCV) RNA after a sustained virological response (SVR) have been reported to be 1-2%. We investigated the reappearance rate of HCV RNA after SVR in chronic hepatitis C (CHC) patients treated with pegylated interferon (PEG-IFN) and ribavirin.

Methods

In total, 292 CHC patients who achieved an SVR after PEG-IFN and ribavirin treatment were included. They were treated with subcutaneous injections of either PEG-IFN-α 2a or 2b plus ribavirin orally. Liver function tests and qualitative HCV RNA assays were performed every 6 months during the follow-up period after an SVR.

Results

Among the 292 patients, 224 (genotype 1, 92; genotype non-1, 132) were followed up for more than 6 months after SVR. These 224 patients were aged 48.1±11.5 years (mean±SD), and 129 of them were male. The median follow-up duration was 18 months (range 6-60 months). The reappearance rate of HCV RNA during follow-up was 0%. Two patients who achieved an SVR developed hepatocellular carcinoma during the follow-up period.

Conclusions

An SVR was maintained in all CHC patients treated with PEG-IFN plus ribavirin during a median follow-up of 18 months. However, a screening test for hepatocellular carcinoma is needed for patients with an SVR.

Citations

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  • Risk of Late Relapse or Reinfection With Hepatitis C Virus After Achieving a Sustained Virological Response: A Systematic Review and Meta-analysis
    Bryony Simmons, Jawaad Saleem, Andrew Hill, Richard D. Riley, Graham S. Cooke
    Clinical Infectious Diseases.2016; 62(6): 683.     CrossRef
  • Long-term maintenance of sustained virological response in liver transplant recipients treated for recurrent hepatitis C
    Francesca Romana Ponziani, Raffaella Viganò, Rosa Maria Iemmolo, Maria Francesca Donato, Maria Rendina, Pierluigi Toniutto, Luisa Pasulo, Maria Cristina Morelli, Patrizia Burra, Lucia Miglioresi, Manuela Merli, Daniele Di Paolo, Stefano Fagiuoli, Antonio
    Digestive and Liver Disease.2014; 46(5): 440.     CrossRef
  • Durability of antiviral therapy for chronic hepatitis C after achieving sustained virological response
    Jeong Heo
    The Korean Journal of Hepatology.2011; 17(3): 180.     CrossRef
  • 9,134 View
  • 39 Download
  • Crossref

Hepatology Elsewhere

Background/Aims
This randomized multicenter trial evaluated individualization of treatment duration with peginterferon alfa-2a 180 microg/wk plus ribavirin 1,000/1,200 mg/day in patients with chronic hepatitis C genotype 1/4 based on the rapidity of virologic response (VR). Methods: Patients with arapid VR (RVR, undetectable hepatitis C virus [HCV]-RNA level (<50 IU/ml at week 4) were treated for 24 weeks, those with an early VR (EVR, no RVR but undetectable HCV-RNA level or >or= 2-log(10) decrease at week 12) were randomized to 48 (group A) or 72 weeks of treatment (group B, peginterferon alfa-2a was reduced to 135 microg/wkafter week 48). Patients without an EVR continued treatment until week 72 if they had undetectable HCV-RNA levels at week 24. The primary end point was relapse, sustained VR (SVR, undetectable HCV-RNA level after 24 weeks of follow-up evaluation) was a secondary end point. Results: Of 551 genotype 1/4 patients starting treatment, 289 were randomized to group A (N=139) or group B(N=150). The relapse rate was 33.6% in group A(95% confidence interval [CI], 24.8%-43.4%) and 18.5% in group B (95% CI, 11.9%-27.6%, P=0.0115 vs group A) and the SVR rate was 51.1% (95% CI,42.5%-59.6%) and 58.6% (95% CI, 50.3%-66.6%, P>0.1), respectively. The overall SVR rate was 50.4% (278 of 551, 95% CI, 46.2%-54.7%), including 115 of 150 patients with an RVR treated for 24 weeks and 4 of 78 patients without an EVR. Conclusions: Extending therapy with peginterferon alfa-2a/ribavirin to 72 weeks decreases the probability of relapse in patients with an EVR. If they can be maintained on extended-duration therapy, SVR rates also may improve.

Citations

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  • The host HLA-A*02 allele is associated with the response to pegylated interferon and ribavirin in patients with chronic hepatitis C virus infection
    Meng Wang, Jian-sheng Li, Yu Ping, Zhi-qin Li, Li-ping Wang, Qian Guo, Zhen Zhang, Dong-li Yue, Fei Wang, Teng-fei Zhang, Mohammad Serajul Islam, Yi Zhang
    Archives of Virology.2015; 160(4): 1043.     CrossRef
  • 5,538 View
  • 17 Download
  • Crossref

Original Articles

Clinical efficacy and safety of the combination therapy of peginterferon alpha and ribavirin in cirrhotic patients with HCV infection
Hong Ryeol Cheong, M.D., Hyun Young Woo, M.D., Jeong Heo, M.D., Ki Tae Yoon, M.D., Dong Uk Kim, M.D., Gwang Ha Kim, M.D., Dae Hwan Kang, M.D., Geun Am Song, M.D., Mong Cho, M.D.
Korean J Hepatol 2010;16(1):38-48.
Published online March 26, 2010
DOI: https://doi.org/10.3350/kjhep.2010.16.1.38
Background/Aims
The combination therapy of peginterferon (PEG-IFN) and ribavirin is the standard treatment for hepatitis C virus (HCV) infection. However, few trials have involved patients with cirrhosis. The purpose of this study was to elucidate the efficacy and safety of treatment with PEG-IFN and ribavirin in patients with cirrhosis associated with HCV infection. Method: A total of 65 patients were treated with PEG-IFN alpha-2a/ribavirin (n=32) or PEG-IFN alpha-2b/ribavirin (n=33). PEG-IFN alpha-2a and PEG-IFN alpha-2b were administered at doses of 180 μg/week and 1.5 μg/kg/week, respectively, and ribavirin was administered orally at doses of 800-1200 mg. Patients with HCV genotype 1 and genotype non-1 were treated for 48 and 24 weeks, respectively. The treatment response was assessed based on the sustained virologic response (SVR). Results: The early virologic response (EVR), end-of-treatment response (ETR), and SVR were 70.0%, 52.0%, and 24.0%, respectively, in genotype 1 (n=50). In genotype non-1 (n=15), the ETR was 53.3% and the SVR was 33.3%. The overall SVR did not differ with genotype (1vs non-1, 24.0%vs.33.3%; P=0.471) or between decompensated cirrhosis and compensated cirrhosis (20.0%vs.27.3%, P=0.630). Ten patients developed cirrhotic complications during the treatment, and 11 stopped treatment due to treatment -related adverse events. Conclusion: The combination therapy of PEG-IFN and ribavirin exhibited a low efficacy in cirrhotic patients with HCV infection and was associated with frequent serious complications. However, with careful management of complications, the therapy may have a considerable efficacy in some patients with cirrhosis and HCV infection. (Korean J Hepatol 2010;16:38-48

Citations

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  • Favorable Outcomes of Chinese HCV-Related Cirrhotic Patients with Sustained Virological Response after Pegylated Interferon Plus Ribavirin Treatment
    Geng-lin Zhang, You-ming Chen, Ting Zhang, Qing-xian Cai, Xiao-hong Zhang, Zhi-xing Zhao, Chao-shuang Lin, Zhi-liang Gao
    BioMed Research International.2017; 2017: 1.     CrossRef
  • Renewed 2015 Clinical Practice Guidelines for Management of Hepatitis C by Korean Association for the Study of the Liver; What Has Been Changed? - Treatment of Patients with Decompensated Cirrhosis
    Geum-Youn Gwak
    The Korean Journal of Gastroenterology.2016; 67(3): 137.     CrossRef
  • KASL clinical practice guidelines: management of hepatitis C

    Clinical and Molecular Hepatology.2016; 22(1): 76.     CrossRef
  • Treatment Response and Long-Term Outcome of Peginterferon α and Ribavirin Therapy in Korean Patients with Chronic Hepatitis C
    Chang Ho Jung, Soon Ho Um, Tae Hyung Kim, Sun Young Yim, Sang Jun Suh, Hyung Joon Yim, Yeon Seok Seo, Hyuk Soon Choi, Hoon Jai Chun
    Gut and Liver.2016; 10(5): 808.     CrossRef
  • Treatment of Hepatitis C in Special Conditions: Liver Cirrhosis
    Geum-Youn Gwak
    Korean Journal of Medicine.2015; 88(6): 643.     CrossRef
  • Pegylated interferon α‐2a plus ribavirin for decompensated hepatitis C virus‐related cirrhosis: relationship between efficacy and cumulative dose
    Yan Xu, Wenqian Qi, Xu Wang, Ping Zhao, Yonggui Zhang, Qian Zhang, Shaoyou Qin, Jiangbin Wang
    Liver International.2014; 34(10): 1522.     CrossRef
  • KASL clinical practice guidelines: Management of Hepatitis C

    Clinical and Molecular Hepatology.2014; 20(2): 89.     CrossRef
  • Clinical and epidemiological features of hepatitis C virus infection in South Korea: A prospective, multicenter cohort study
    Mun Hyuk Seong, Ho Kil, Young Seok Kim, Si Hyun Bae, Youn Jae Lee, Han Chu Lee, Byung Hak Kang, Sook-Hyang Jeong
    Journal of Medical Virology.2013; 85(10): 1724.     CrossRef
  • A Case of Interstitial Pneumonitis and Pancytopenia Following the Combination Therapy of Pegylated Interferon and Ribavirin
    Ji-Hyun Suh, Sung Hwahn Hahn, Ji Eun Lee, Jin Hyung Han, Kyung-Mook Kim, Doh-Hyung Kim, Yon-Seop Kim, Jae-Suk Park, Young-Koo Jee
    Tuberculosis and Respiratory Diseases.2011; 70(1): 69.     CrossRef
  • 6,322 View
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A comparison of 24- vs. 48-week peginterferon plus ribavirin in patients with genotype 1 chronic hepatitis C
Mi Na Kim, M.D.1, Ki Tae Yoon, M.D.2,3, Jun Yong Park, M.D.1,3, Do Young Kim, M.D.1,3, Sang Hoon Ahn, M.D.1,3, Chae Yoon Chon, M.D.1,3, Kwang-Hyub Han, M.D.1,3
Korean J Hepatol 2009;15(4):496-503.
Published online December 31, 2009
DOI: https://doi.org/10.3350/kjhep.2009.15.4.496
Background/Aims
The standard therapy for patients with genotype 1 chronic hepatitis C (CHC) is a combination of peginterferon and ribavirin for 48 weeks. However, the most appropriate duration of treatment remains to be established because of treatment-related side effects and cost. The aim of this study was to compare the efficacies of 24- and 48-week treatments, and to assess the efficacy of split 24-week therapy (a further 24 weeks of treatment in patients with relapse after the initial 24 weeks of treatment). Methods: A total of 130 patients with genotype 1 CHC was treated between June 2004 and December 2006. Patients with undetectable HCV RNA at 24 weeks of treatment (as assessed by qualitative PCR assay; n=101 patients) were allowed to choose either 24 or 48 weeks as the duration of their treatment; 51 patients chose the 24-week treatment regimen and the remainder chose the 48-week regimen. Patients who relapsed after 24 weeks of treatment were treated for further 24 weeks. The sustained virologic response (SVR) of each treatment group was analyzed. Results: The SVR rate was higher in patients treated for 48 weeks than in those treated for 24 weeks (74.0% vs. 52.9%, P=0.028). In the multivariate analysis, age < 50 years, platelets ≥ 150,000/mm3, and treatment duration for 48 weeks remained significant independent predictors of SVR. Fourteen of the 24 patients who relapsed in the 24-week treatment group received split 24-week therapy, and 6 patients (42.9%) achieved SVR. The overall SVR rate did not differ significantly between the 24-week treatment group, including those who underwent 24-week split therapy (64.7%), and the 48-week treatment group (64.7% vs. 74%, P=0.311). Conclusions: The 24-week plus additional split 24-week therapy following failure is a useful treatment strategy for patients with genotype 1 CHC. (Korean J Hepatol 2009;15:496-503)

Citations

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  • Comparison of Efficacy of Peginterferon and Ribavirin Combination Therapy for Chronic Hepatitis C among Korean, Caucasian and Other Asians
    Kyung-Ah Kim
    The Korean Journal of Gastroenterology.2012; 60(5): 273.     CrossRef
  • Efficacy of Peginterferon and Ribavirin Combination Therapy of Chronic Hepatitis C: A Pooled Analysis
    Soo Yong Park, Min Young Rim, In Ku Yo, Min Su Ha, Ju Seung Kim, Ji Won Lee, Young Kul Jung, Oh Sang Kwon, Yun Soo Kim, Duck Joo Choi, Ju Hyun Kim
    The Korean Journal of Gastroenterology.2012; 60(5): 306.     CrossRef
  • 5,818 View
  • 18 Download
  • Crossref
Impact of adherence to peginterferon-ribavirin combination therapy in chronic hepatitis C patients on achieving a sustained virologic response
Soung Won Jeong, M.D., Jin Dong Kim, M.D.1, Hyun Young Woo, M.D.1, Chan Ran You, M.D.1, Sung Won Lee, M.D.1, Myeong Jun Song, M.D.1, Jung Won Jang, M.D.1, Si Hyun Bae, M.D.1, Jong Young Choi, M.D.1, Seung Kew Yoon, M.D.1
Korean J Hepatol 2009;15(3):338-349.
Published online September 30, 2009
DOI: https://doi.org/10.3350/kjhep.2009.15.3.338
Background/Aims
Various predictive factors for peginterferon alpha and ribavirin therapy in chronic hepatitis C have been reported, but the effect of adherence to therapy has not been established. We investigated how adherence affects the sustained virologic response (SVR). Methods: We analyzed 92 chronic hepatitis C patients receiving peginterferon alpha and ribavirin combination therapy. Patients were first identified as having either genotype 1 or genotype non-1 infection and then categorized into three groups according to their adherence to the treatment protocol: (1) patients who received ≥80% of the recommended dosage of both peginterferon alpha and ribavirin for ≥80% of the intended duration of therapy, (2) patients who received <60% of the recommended dosage of both peginterferon alpha and ribavirin for <60% of the intended duration of therapy, and (3) patients who were not included in either group 1 or 2. Results: The rates of early virologic response, end of treatment response, and SVR differed significantly with the degree of adherence to the treatment. The SVRs of genotype 1 patients were 86.7%, 26.7%, and 66.7% in groups 1, 2, and 3, respectively (P=0.003), and those of genotype non-1 were 100%, 16.7%, and 88.9%, respectively (P<0.001). Conclusions: Adherence to therapy is a key factor in achieving an SVR. Supportive strategies to improve adherence will increase overall SVR rates. (Korean J Hepatol 2009;15:338-349)

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  • Long-Term Follow-up of Liver Transplant Recipients Treated With Direct-Acting Antiviral Agents for Hepatitis C Recurrence After Transplantation
    Tomasz Cieciura, Ewa Hryniewiecka, Bartosz Foroncewicz, Ziemowit Strzelczyk, Michal Ciszek, Leszek Paczek
    Transplantation Proceedings.2020; 52(8): 2468.     CrossRef
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    Tania M. Welzel, Min Yang, Gautam Sajeev, Yaozhu J. Chen, Brett Pinsky, Yanjun Bao, Eric Q. Wu, Douglas Dieterich
    Advances in Therapy.2019; 36(9): 2475.     CrossRef
  • After successful hepatitis C virus antiviral therapy: It looks that normal alanine aminotransferase level is not the normal
    Mohamed El Kassas, Mohamed Alboraie, Aya Mostafa, Reem Ezzat, Adel El Tahan, Shimaa Afify, Ahmed Sweedy, Ibrahim Kabbash, Gamal Esmat
    Journal of Clinical Laboratory Analysis.2018;[Epub]     CrossRef
  • KASL clinical practice guidelines: management of hepatitis C

    Clinical and Molecular Hepatology.2016; 22(1): 76.     CrossRef
  • KASL clinical practice guidelines: Management of Hepatitis C

    Clinical and Molecular Hepatology.2014; 20(2): 89.     CrossRef
  • Polymorphisms nearInterleukin 28BGene Are Not Associated with Hepatitis B Virus Clearance, Hepatitis B e Antigen Clearance and Hepatocellular Carcinoma Occurrence
    Dong Hyeon Lee, Yuri Cho, Ji Yeon Seo, Jung Hee Kwon, Eun Ju Cho, Eun Sun Jang, Min-Sun Kwak, Jae Youn Cheong, Sung Won Cho, Jeong-Hoon Lee, Su Jong Yu, Jung-Hwan Yoon, Hyo-Suk Lee, Chung Yong Kim, Hyoung Doo Shin, Yoon Jun Kim
    Intervirology.2013; 56(2): 84.     CrossRef
  • Adherence and Completion in Hepatitis C Management
    Rhoda Redulla, Sharon Dudley-Brown
    Gastroenterology Nursing.2013; 36(1): 53.     CrossRef
  • Efficacy of Peginterferon and Ribavirin Combination Therapy of Chronic Hepatitis C: A Pooled Analysis
    Soo Yong Park, Min Young Rim, In Ku Yo, Min Su Ha, Ju Seung Kim, Ji Won Lee, Young Kul Jung, Oh Sang Kwon, Yun Soo Kim, Duck Joo Choi, Ju Hyun Kim
    The Korean Journal of Gastroenterology.2012; 60(5): 306.     CrossRef
  • Rapid normalization of alanine aminotransferase predicts viral response during combined peginterferon and ribavirin treatment in chronic hepatitis C patients
    Yun Jung Kim, Byoung Kuk Jang, Eun Soo Kim, Kyung Sik Park, Kwang Bum Cho, Woo Jin Chung, Jae Seok Hwang
    The Korean Journal of Hepatology.2012; 18(1): 41.     CrossRef
  • Importance of Medication Adherence to Peginterferon-Ribavirin Combination Therapy in Patients with Chronic Hepatitis C
    Pyung Gohn Goh, Min Jung Kim, Hye Jin Kim, Hyuk Soo Eun, Eui Sik Kim, Yun Jeung Kim, Soo Youn Lee, Hee Seok Moon, Eaum Seok Lee, Seok Hyun Kim, Byung Seok Lee, Heon Young Lee
    The Korean Journal of Gastroenterology.2011; 57(5): 294.     CrossRef
  • Polymorphism near the IL28B gene in Korean hepatitis C virus-infected patients treated with peg-interferon plus ribavirin
    KwangSoo Lyoo, Myeong Jun Song, Wonhee Hur, Jung Eun Choi, Sung Woo Hong, Chang Wook Kim, Si Hyun Bae, Jong Young Choi, Sang Wook Choi, Eui-Cheol Shin, Seung Kew Yoon
    Journal of Clinical Virology.2011; 52(4): 363.     CrossRef
  • 5,518 View
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Durability of a sustained virologic response in combination therapy with interferon/peginterferon and ribavirin for chronic hepatitis C
Chul Hyun Kim , Byung Do Park , Jin Woo Lee , Young Soo Kim , Seok Jeong , Don Haeng Lee , Hyung Gil Kim , Yong Woon Shin , Key Sook Kwon , Jung Il Lee
Korean J Hepatol 2009;15(1):70-79.
Published online March 31, 2009
DOI: https://doi.org/10.3350/kjhep.2009.15.1.70
Backgrounds/Aims
The ultimate goal of antiviral therapy using interferon/pegylated interferon combined with ribavirin in chronic C-viral hepatitis is to achieve a sustained virologic response (SVR). Several studies have shown that the reappearance rate of hepatitis C virus (HCV) RNA in serum after the achievement of an SVR is less than 1%; the durability of an SVR in Korean patients is not known. The aim of this study was to determine the durability of the virologic response in chronic hepatitis C patients with an SVR to antiviral therapy. Methods: A total of 156 patients who were treated successfully with interferon/peginterferon and ribavirin were evaluated retrospectively. Patients received either subcutaneous conventional interferon alpha 3×10(6) units three times a week or subcutaneous pegylated interferon (α-2a: 180 μg, α-2b: 80-100 μg) once a week in combination with ribavirin at 600-1,200 mg daily (depending on body weight). Patients with HCV genotype 1 were treated for 48 weeks, whereas those with non-genotype 1 were treated for 24 weeks. Results: Eighty-two patients underwent treatment with conventional interferon and ribavirin, whereas 74 patients were treated with pegylated interferon and ribavirin. An SVR was achieved in 73 patients (73/156, 46.8%). HCV RNA reappeared in eight patients (8/73, 11.0%, detected by qualitative PCR), including one patient with persistent viremia (1/73, 1.4%). Conclusions: Reappearance of HCV RNA after earlier achievement of an SVR might appear more frequently than previously reported. Close follow-up of these patients is recommended and the implication of temporary viremia should be determined in the future. (Korean J Hepatol 2008;15:70-79)

Citations

Citations to this article as recorded by  Crossref logo
  • Risk of Late Relapse or Reinfection With Hepatitis C Virus After Achieving a Sustained Virological Response: A Systematic Review and Meta-analysis
    Bryony Simmons, Jawaad Saleem, Andrew Hill, Richard D. Riley, Graham S. Cooke
    Clinical Infectious Diseases.2016; 62(6): 683.     CrossRef
  • Efficacy of Peginterferon and Ribavirin Combination Therapy of Chronic Hepatitis C: A Pooled Analysis
    Soo Yong Park, Min Young Rim, In Ku Yo, Min Su Ha, Ju Seung Kim, Ji Won Lee, Young Kul Jung, Oh Sang Kwon, Yun Soo Kim, Duck Joo Choi, Ju Hyun Kim
    The Korean Journal of Gastroenterology.2012; 60(5): 306.     CrossRef
  • Longitudinal changes of the laboratory data of chronic hepatitis C patients with sustained virological response on long‐term follow‐up
    D. Maruoka, F. Imazeki, M. Arai, T. Kanda, K. Fujiwara, O. Yokosuka
    Journal of Viral Hepatitis.2012;[Epub]     CrossRef
  • Chronic Hepatitis C
    Jae Young Jang, Raymond T. Chung
    Gut and Liver.2011; 5(2): 117.     CrossRef
  • Durability of a sustained virologic response in patients with chronic hepatitis C treated with peginterferon and ribavirin
    Kyung-Ah Kim
    The Korean Journal of Hepatology.2011; 17(1): 84.     CrossRef
  • Durability of antiviral therapy for chronic hepatitis C after achieving sustained virological response
    Jeong Heo
    The Korean Journal of Hepatology.2011; 17(3): 180.     CrossRef
  • Durability of a sustained virological response in chronic hepatitis C patients treated with pegylated interferon alfa and ribavirin
    Sang Bun Choi, Youn Jae Lee, Jae Ik Lee, Young Jin Song, Byoung Jin Choi, Jong Han Kim, Eun Uk Jung, Sung Jae Park, Sang Heon Lee, Ji Hyun Kim, Jung Sik Choi, Sam Ryong Jee, Sang Yong Seol
    The Korean Journal of Hepatology.2011; 17(3): 183.     CrossRef
  • Durability of Sustained Virologic Response in Chronic Hepatitis C: Analysis of Factors Related to Relapse after Sustained Virologic Response with Peginterferon Plus Ribavirin Combination Therapy
    Jang Eun Lee, Na Ri Yoon, Jin Dong Kim, Myeong Jun Song, Jung Hyun Kwon, Si Hyun Bae, Jong Young Choi, Sung Won Jeong, Seung Kew Yoon
    The Korean Journal of Gastroenterology.2011; 57(3): 173.     CrossRef
  • Long-Term Effects of Antiviral Therapy in Patients with Chronic Hepatitis C
    Tatehiro Kagawa, Emmet B. Keeffe
    Hepatitis Research and Treatment.2010; 2010: 1.     CrossRef
  • 5,338 View
  • 26 Download
  • Crossref
Efficacy of initial treatment with peginterferon alpha-2a versus peginterferon alpha-2b in combination with ribavirin in naive chronic hepatitis C patients Living in Daejeon and Chungcheong Province in Korea: A comparative study
Jeong Il Kim, M.D, Seok Hyun Kim, M.D., Byung Seok Lee, M.D., Heon Young Lee, M.D., Tae Hee Lee, M.D.1, Young Woo Kang, M.D.1, Hyang Ie Lee, M.D.2, An Na Kim, M.D.2, Soon Woo Nam, M.D.3, Byeong Chool Park, M.D.4, Hee Bok Chae, M.D.4, Seok Bae Kim, M.D.5, Il Han Song, M.D.5, Ji Young Park, M.D.6, Hong Su Kim, M.D.6
Korean J Hepatol 2008;14(4):493-502.
Published online December 31, 2008
DOI: https://doi.org/10.3350/kjhep.2008.14.4.493
Backgrounds/Aims
Peginterferon alpha-2a or -2b is the standard treatment regimen in chronic hepatitis C. However, there have been few comparative studies of the efficacies of these two types of peginterferon. We evaluated their efficacies in combination with ribavirin as a initial treatment for chronic hepatitis C. Methods: Ninety-seven patients were treated with peginterferon alpha-2a (180 ?g/week, n=48) or peginterferon alpha-2b(1.5 ?g/kg/week, n=49) plus ribavirin (800 mg/day for 24 weeks in genotype non-1 or 1,000-1,200 mg/day for 48 weeks in genotype 1). Virologic responses including the early virologic response (EVR), end-of-treatment response (ETR), sustained virologic response (SVR), and adverse effects were analyzed retrospectively. Results: The virologic response rates did not differ significantly between peginterferon alpha-2a and -2b: 89.6% and 89.7% for EVR, 79.2% and 79.5% for ETR, 72.9% and 73.5% for SVR, respectively. Analysis of the virologic responses according to genotype also revealed no significant differences in SVR between peg-interferon alpha-2a and -2b (59.3% vs. 59.7% for genotype 1 and 90.5% vs. 83.3% for genotype non-1, respectively), or in adverse effects including flu-like symptom, rash, itching, neutropenia, and thrombocytopenia. Conclusions: We found no significant differences in therapeutic efficacies and adverse effects between the alpha-2a and -2b types of peginterferon as the initial treatment regimen in naive chronic hepatitis C patients. (Korean J Hepatol 2008;14:493-502)

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  • Advanced fibrosis is not a negative pretreatment predictive factor for genotype 2 or 3 chronic hepatitis C patients
    Hyun Seok Lee, Young Oh Kweon, Won Young Tak, Soo Young Park, Eun Jung Kang, Yu Lim Lee, Hae Min Yang, Hyun Woo Park
    Clinical and Molecular Hepatology.2013; 19(2): 148.     CrossRef
  • Role of Interleukin 28B-related Gene Polymorphisms in Chronic Hepatitis C and the Response to Antiviral Therapy in Koreans
    Young Kul Jung, Ji Hoon Kim, Sung-Min Ahn, Jae Won Yang, Sang Jin Park, Jong Woo Kim, Jong Eun Yeon, Oh Sang Kwon, Yun Soo Kim, Duck Joo Choi, Ju Hyun Kim, Kwan Soo Byun
    Journal of Clinical Gastroenterology.2013; 47(7): 644.     CrossRef
  • Pegylated Interferon-α2a and Ribavirin versus Pegylated Interferon-α2b and Ribavirin in Chronic Hepatitis C
    Nicolas Flori, Natalie Funakoshi, Yohan Duny, Jean-Christophe Valats, Michael Bismuth, Dimitri Christophorou, Jean-Pierre Daurès, Pierre Blanc
    Drugs.2013; 73(3): 263.     CrossRef
  • Efficacy of Peginterferon and Ribavirin Combination Therapy of Chronic Hepatitis C: A Pooled Analysis
    Soo Yong Park, Min Young Rim, In Ku Yo, Min Su Ha, Ju Seung Kim, Ji Won Lee, Young Kul Jung, Oh Sang Kwon, Yun Soo Kim, Duck Joo Choi, Ju Hyun Kim
    The Korean Journal of Gastroenterology.2012; 60(5): 306.     CrossRef
  • Efficacy of peginterferon and ribavirin is associated with the IL28B gene in Korean patients with chronic hepatitis C
    Seok Hoo Jeong, Young Kul Jung, Jae Won Yang, Sang Jin Park, Jong Woo Kim, Oh Sang Kwon, Yun Soo Kim, Duck Joo Choi, Ju Hyun Kim
    Clinical and Molecular Hepatology.2012; 18(4): 360.     CrossRef
  • Recent trends in the treatment of chronic hepatitis C
    Dae Won Jun, Won Young Tak, Si Hyun Bae, Youn Jae Lee
    The Korean Journal of Hepatology.2012; 18(1): 22.     CrossRef
  • Peginterferon alpha and ribavirin combination therapy in patients with hepatitis C virus-related liver cirrhosis
    Kyung Hoon Kim, Byoung Kuk Jang, Woo Jin Chung, Jae Seok Hwang, Young Oh Kweon, Won Young Tak, Heon Ju Lee, Chang Hyeong Lee, Jeong Ill Suh
    The Korean Journal of Hepatology.2011; 17(3): 220.     CrossRef
  • Current status of liver disease in Korea: Hepatitis C
    Young-Suk Lim
    The Korean Journal of Hepatology.2009; 15(Suppl 6): S25.     CrossRef
  • Treatment of chronic hepatitis C: Efficacy of initial treatment of peginterferon alpha-2a versus peginterferon alpha-2b plus ribavirin in naive chronic hepatitis C patients
    Youn Jae Lee
    The Korean Journal of Hepatology.2008; 14(4): 443.     CrossRef
  • 5,419 View
  • 21 Download
  • Crossref

Editorial

Original Articles

Effects of pegylated interferon and ribavirin in Korean patients with chronic hepatitis C virus infection
Myoung Joo Kang, M.D., Eun Uk Jung, M.D., Sang Won Park, M.D., Paul Choi, M.D., Ji Hyun Kim, M.D., Sung Jae Park, M.D., Eun Taek Park, M.D., Youn Jae Lee, M.D., Sang Hyuk Lee, M.D., Sang Yong Seol, M.D.
Korean J Hepatol 2008;14(3):318-330.
Published online September 30, 2008
DOI: https://doi.org/10.3350/kjhep.2008.14.3.318
Background/Aims
We assessed the efficacy and safety of pegylated interferon (peginterferon) plus ribavirin and identified the predictors of a sustained virologic response (SVR) in Korean patients with chronic hepatitis C virus infection. Methods: A total of 192 patients with chronic hepatitis C, treated with both peginterferon (n=141) or conventional interferon (n=51) and ribavirin, were analyzed retrospectively. Peginterferon alfa-2a (180 μg/week) or -2b (1.5 μg/kg/week) or interferon alfa-2a (3 MIU thrice weekly) was administered in combination with ribavirin at 1,000-1,200 mg/day for 48 weeks for genotype 1 and at 800 mg/day for 24 weeks for genotypes 2 and 3. Results: The overall SVR rate was 80.9% (114/141) in the peginterferon group and 52.9% (27/51) in the interferon group (P=0.0001). The SVR rate in genotype 1 was 69.5% (41/59) in the peginterferon group and 31.6% (6/19) in the interferon group (P=0.0033), whereas in genotype 2 or 3 it was 89.0% (73/82) in the peginterferon group and 65.6% (21/32) in the interferon group (P=0.0032). The predictors of SVR in the peginterferon group were genotype, absence of cirrhosis, and early virologic response (P<0.05). Conclusions: In Korean patients with chronic hepatitis C, a regimen of peginterferon and ribavirin was more effective than a regimen of conventional interferon and ribavirin. This result is comparable to those from studies on Western patients as an initial treatment for chronic hepatitis C. (Korean J Hepatol 2008;14: 318-330)

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    Baek Gyu Jun, Eui Ju Park, Woong Cheul Lee, Jae Young Jang, Soung Won Jeong, Young Don Kim, Gab Jin Cheon, Young Sin Cho, Sae Hwan Lee, Hong Soo Kim, Yun Nah Lee, Sang Gyune Kim, Young Seok Kim, Boo Sung Kim
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    Sang Bong Ahn, Dae Won Jun, Sang Gyune Kim, Sae Hwan Lee, Hyun Phil Shin, Won Hyeok Choe, Ja Kyung Kim, Kyu Sik Jung, Do Young Kim, Jae-Jun Shim, Soo Young Park, Yeon Seok Seo, Won Kim, Jae Il Chung
    European Journal of Internal Medicine.2015; 26(4): 292.     CrossRef
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    Paulina Jackowiak, Karolina Kuls, Lucyna Budzko, Anna Mania, Magdalena Figlerowicz, Marek Figlerowicz
    Infection, Genetics and Evolution.2014; 21: 67.     CrossRef
  • KASL clinical practice guidelines: Management of Hepatitis C

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  • Advanced fibrosis is not a negative pretreatment predictive factor for genotype 2 or 3 chronic hepatitis C patients
    Hyun Seok Lee, Young Oh Kweon, Won Young Tak, Soo Young Park, Eun Jung Kang, Yu Lim Lee, Hae Min Yang, Hyun Woo Park
    Clinical and Molecular Hepatology.2013; 19(2): 148.     CrossRef
  • Is peginterferon and ribavirin therapy effective in Korean patients with chronic hepatitis C?
    Young Kul Jung, Ju Hyun Kim
    Clinical and Molecular Hepatology.2013; 19(1): 26.     CrossRef
  • Efficacy of peginterferon and ribavirin is associated with the IL28B gene in Korean patients with chronic hepatitis C
    Seok Hoo Jeong, Young Kul Jung, Jae Won Yang, Sang Jin Park, Jong Woo Kim, Oh Sang Kwon, Yun Soo Kim, Duck Joo Choi, Ju Hyun Kim
    Clinical and Molecular Hepatology.2012; 18(4): 360.     CrossRef
  • Efficacy and Tolerability of Peginterferon Alpha Plus Ribavirin in the Routine Daily Treatment of Chronic Hepatitis C Patients in Korea: A Multi-Center, Retrospective Observational Study
    Sang Hoon Park, Choong Kee Park, Jin Woo Lee, Young Seok Kim, Sook-Hyang Jeong, Yun Soo im, Ju Hyun Kim, Seong Gyu Hwang, Kyu Sung Rim, Hyung Joon Yim, Jae Youn Cheong, Sung Won Cho, June Sung Lee, Young Min Park, Jeong Won Jang Chun Kyon Lee, Joo Hyun Sh
    Gut and Liver.2012; 6(1): 98.     CrossRef
  • Efficacy of Peginterferon and Ribavirin Combination Therapy of Chronic Hepatitis C: A Pooled Analysis
    Soo Yong Park, Min Young Rim, In Ku Yo, Min Su Ha, Ju Seung Kim, Ji Won Lee, Young Kul Jung, Oh Sang Kwon, Yun Soo Kim, Duck Joo Choi, Ju Hyun Kim
    The Korean Journal of Gastroenterology.2012; 60(5): 306.     CrossRef
  • A reduced dose of ribavirin does not influence the virologic response during pegylated interferon alpha-2b and ribavirin combination therapy in patients with genotype 1 chronic hepatitis C
    Byung Chul You, Young Seok Kim, Hun il Kim, Se Hun Kim, Seung Sik Park, Yu Ri Seo, Sang Gyune Kim, Se Whan Lee, Hong Soo Kim, Soung Won Jeong, Jae Young Jang, Boo Sung Kim
    Clinical and Molecular Hepatology.2012; 18(3): 272.     CrossRef
  • A Case of Interstitial Pneumonitis and Pancytopenia Following the Combination Therapy of Pegylated Interferon and Ribavirin
    Ji-Hyun Suh, Sung Hwahn Hahn, Ji Eun Lee, Jin Hyung Han, Kyung-Mook Kim, Doh-Hyung Kim, Yon-Seop Kim, Jae-Suk Park, Young-Koo Jee
    Tuberculosis and Respiratory Diseases.2011; 70(1): 69.     CrossRef
  • Role of vitamin D in chronic hepatitis C
    Tae Yeob Kim
    The Korean Journal of Hepatology.2011; 17(2): 170.     CrossRef
  • Clinical features and treatment efficacy of peginterferon alfa plus ribavirin in chronic hepatitis C patients coinfected with hepatitis B virus
    Yu Jin Kim, Jin Woo Lee, Yun Soo Kim, Sook-Hyang Jeong, Young Seok Kim, Hyung Joon Yim, Bo Hyun Kim, Chun Kyon Lee, Choong Kee Park, Sang Hoon Park
    The Korean Journal of Hepatology.2011; 17(3): 199.     CrossRef
  • 24 Weeks Treatment with Pegylated Interferon Alfa Plus Ribavirin May Be Possible in Genotype 1 Chronic Hepatitis C Patients with Rapid Virological Response Who Have Low Pretreatment Viremia
    Sung Soo Moon, Hyoun Gu Kang, Jeong Ah Seo, Eun Uk Jung, Sang Heon Lee, Sung Jae Park, Youn Jae Lee, Sang Yong Seol
    The Korean Journal of Gastroenterology.2010; 56(1): 33.     CrossRef
  • Impact of adherence to peginterferon-ribavirin combination therapy in chronic hepatitis C patients on achieving a sustained virologic response
    Soung Won Jeong, Jin Dong Kim, Hyun Young Woo, Chan Ran You, Sung Won Lee, Myeong Jun Song, Jung Won Jang, Si Hyun Bae, Jong Young Choi, Seung Kew Yoon
    The Korean Journal of Hepatology.2009; 15(3): 338.     CrossRef
  • Current status of liver disease in Korea: Hepatitis C
    Young-Suk Lim
    The Korean Journal of Hepatology.2009; 15(Suppl 6): S25.     CrossRef
  • Treatment of chronic hepatitis C: Efficacy of initial treatment of peginterferon alpha-2a versus peginterferon alpha-2b plus ribavirin in naive chronic hepatitis C patients
    Youn Jae Lee
    The Korean Journal of Hepatology.2008; 14(4): 443.     CrossRef
  • 6,480 View
  • 39 Download
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Clinical outcome of pegylated interferon and ribavirin therapy for chronic hepatitis C
Kyoung Tae Kim , Sang Young Han , Jong Han Kim , Hyun Ah Yoon , Yang Hyun Baek , Min Ji Kim , Sung Wook Lee , Jin Seok Jang , Jong Hun Lee , Myung Hwan Roh
Korean J Hepatol 2008;14(1):36-45.
Published online March 20, 2008
DOI: https://doi.org/10.3350/kjhep.2008.14.1.36
Background/Aims
The purpose of this study is to elucidate the efficacy and safety of combined peginterferon and ribavirin therapy in Korean patients with chronic HCV infection. Methods: We retrospectively analyzed the clinical records of 84 patients. Thirty five patients with genotype 1 HCV infection were treated with peginterferon α-2a 180 μg/week and ribavirin 1,000-1,200 mg/day for 48 weeks, and 49 patients with genotype non-1 were treated with peginterferon α-2a 180 μg/week and ribavirin 800 mg/day for 24 weeks. Results: An early virologic response was seen in 87.0% of patients with genotype 1 HCV. An end of treatment response (ETR) was seen in 82.6% and 97.6% of patients with genotype 1 and genotype non-1, respectively. An overall sustained virologic response (SVR) was seen in 53 patients (82.8%) of the 64 patients: in 16 (69.6%) of 23 patients with genotype 1 and in 37 (90.2%) of 41 patients with genotype non-1. An end of treatment biochemical response was seen in 58 patients (90.6%) [genotype 1, 20 patients (87.0%); genotype non-1, 38 patients (92.7%)], and a sustained biochemical response was achieved in 49 patients (76.6%) [genotype 1, 14 patients (60.9%); genotype non-1, 35 patients (85.4%)]. Independent factors affecting an SVR were HCV genotype and the baseline HCV RNA level. Conclusions: This study shows that a combination therapy of peginterferon and ribavirin is highly effective for chronic HCV infection, producing a high SVR and ETR. (Korean J Hepatol 2008;14:36-45)

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  • All‐oral daclatasvir plus asunaprevir for chronic hepatitis C virus (HCV) genotype 1b infection: a sub‐analysis in Asian patients from the HALLMARK DUAL study
    Jia‐Horng Kao, Youn‐Jae Lee, Jeong Heo, Sang‐Hoon Ahn, Young‐Suk Lim, Cheng‐Yuan Peng, Ting‐Tsung Chang, Anne Torbeyns, Eric Hughes, Rafia Bhore, Stephanie Noviello
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    Shiaw-Hooi Ho, Kee-Peng Ng, Harvinder Kaur, Khean-Lee Goh
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  • Lower Incidence of Hepatocellular Carcinoma and Cirrhosis in Hepatitis C Patients with Sustained Virological Response by Pegylated Interferon and Ribavirin
    Chansoo Moon, Kyu Sik Jung, Do Young Kim, Oidov Baatarkhuu, Jun Yong Park, Beom Kyung Kim, Seung Up Kim, Sang Hoon Ahn, Kwang-Hyub Han
    Digestive Diseases and Sciences.2015; 60(2): 573.     CrossRef
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    Korean Journal of Adult Nursing.2014; 26(2): 214.     CrossRef
  • Advanced fibrosis is not a negative pretreatment predictive factor for genotype 2 or 3 chronic hepatitis C patients
    Hyun Seok Lee, Young Oh Kweon, Won Young Tak, Soo Young Park, Eun Jung Kang, Yu Lim Lee, Hae Min Yang, Hyun Woo Park
    Clinical and Molecular Hepatology.2013; 19(2): 148.     CrossRef
  • Efficacy and Tolerability of Peginterferon Alpha Plus Ribavirin in the Routine Daily Treatment of Chronic Hepatitis C Patients in Korea: A Multi-Center, Retrospective Observational Study
    Sang Hoon Park, Choong Kee Park, Jin Woo Lee, Young Seok Kim, Sook-Hyang Jeong, Yun Soo im, Ju Hyun Kim, Seong Gyu Hwang, Kyu Sung Rim, Hyung Joon Yim, Jae Youn Cheong, Sung Won Cho, June Sung Lee, Young Min Park, Jeong Won Jang Chun Kyon Lee, Joo Hyun Sh
    Gut and Liver.2012; 6(1): 98.     CrossRef
  • Recent trends in the treatment of chronic hepatitis C
    Dae Won Jun, Won Young Tak, Si Hyun Bae, Youn Jae Lee
    The Korean Journal of Hepatology.2012; 18(1): 22.     CrossRef
  • Efficacy of Peginterferon and Ribavirin Combination Therapy of Chronic Hepatitis C: A Pooled Analysis
    Soo Yong Park, Min Young Rim, In Ku Yo, Min Su Ha, Ju Seung Kim, Ji Won Lee, Young Kul Jung, Oh Sang Kwon, Yun Soo Kim, Duck Joo Choi, Ju Hyun Kim
    The Korean Journal of Gastroenterology.2012; 60(5): 306.     CrossRef
  • A reduced dose of ribavirin does not influence the virologic response during pegylated interferon alpha-2b and ribavirin combination therapy in patients with genotype 1 chronic hepatitis C
    Byung Chul You, Young Seok Kim, Hun il Kim, Se Hun Kim, Seung Sik Park, Yu Ri Seo, Sang Gyune Kim, Se Whan Lee, Hong Soo Kim, Soung Won Jeong, Jae Young Jang, Boo Sung Kim
    Clinical and Molecular Hepatology.2012; 18(3): 272.     CrossRef
  • Peginterferon alpha and ribavirin combination therapy in patients with hepatitis C virus-related liver cirrhosis
    Kyung Hoon Kim, Byoung Kuk Jang, Woo Jin Chung, Jae Seok Hwang, Young Oh Kweon, Won Young Tak, Heon Ju Lee, Chang Hyeong Lee, Jeong Ill Suh
    The Korean Journal of Hepatology.2011; 17(3): 220.     CrossRef
  • Antiviral Therapy in Patients after Treatment for Hepatitis C-Related Hepatocellular Carcinoma
    Su Rin Shin, Seung Woon Paik, Geum-Youn Gwak, Moon Seok Choi, Joon Hyoek Lee, Kwang Cheol Koh, Byung Chul Yoo
    Gut and Liver.2011; 5(1): 77.     CrossRef
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    Yu Jin Kim, Jin Woo Lee, Yun Soo Kim, Sook-Hyang Jeong, Young Seok Kim, Hyung Joon Yim, Bo Hyun Kim, Chun Kyon Lee, Choong Kee Park, Sang Hoon Park
    The Korean Journal of Hepatology.2011; 17(3): 199.     CrossRef
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    Su Rin Shin, Dong Hyun Sinn, Geum‐Youn Gwak, Moon Seok Cho, Joon Hyoek Lee, Kwang Cheol Koh, Byung Chul Yoo, Seung Woon Paik
    Journal of Gastroenterology and Hepatology.2010; 25(5): 957.     CrossRef
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    Young-Suk Lim
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    Chun-che Lin, Mei-chin Yin
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    Journal of Gastroenterology and Hepatology.2009; 24(3): 336.     CrossRef
  • Effects of pegylated interferon and ribavirin in Korean patients with chronic hepatitis C virus infection
    Myoung Joo Kang, Eun Uk Jung, Sang Won Park, Paul Choi, Ji Hyun Kim, Sung Jae Park, Eun Taek Park, Youn Jae Lee, Sang Hyuk Lee, Sang Yong Seol
    The Korean Journal of Hepatology.2008; 14(3): 318.     CrossRef
  • Efficacy of initial treatment with peginterferon alpha-2a versus peginterferon alpha-2b in combination with ribavirin in naive chronic hepatitis C patients living in Daejeon and Chungcheong Province in Korea: A comparative study
    Jeong Il Kim, Seok Hyun Kim, Byung Seok Lee, Heon Young Lee, Tae Hee Lee, Young Woo Kang, Hyang Ie Lee, An Na Kim, Soon Woo Nam, Byeong Chool Park, Hee Bok Chae, Seok Bae Kim, Il Han Song, Ji Young Park, Hong Su Kim
    The Korean Journal of Hepatology.2008; 14(4): 493.     CrossRef
  • Treatment of chronic hepatitis C: Efficacy of initial treatment of peginterferon alpha-2a versus peginterferon alpha-2b plus ribavirin in naive chronic hepatitis C patients
    Youn Jae Lee
    The Korean Journal of Hepatology.2008; 14(4): 443.     CrossRef
  • 5,648 View
  • 31 Download
  • Crossref
Short-term Therapy with Pegylated Interferon plus Ribavirin for the Chronic Hepatitis C Genotype 2 Patients
Eun Uk Jung , Ji Hun Park , Kyung Im Pae , Suk Woo Kang , Sung Jae Park , Sam Ryong Jee , Eun Tak Park , Youn Jae Lee , Sang Hyuk Lee , Sang Young Seol
Korean J Hepatol 2007;13(3):341-348.
Published online September 20, 2007
DOI: https://doi.org/10.3350/kjhep.2007.13.3.341
Background/Aims
The standard treatment for chronic hepatitis C patients infected with HCV genotype-2 is a combination of pegylated interferon alfa and ribavirin over a 24 week period. It is unclear if a shorter treatment duration is possible for patients showing a rapid virological response (RVR) without compromising the sustained virologic response (SVR) in Korea. Methods: 42 patients chronically infected with the HCV genotype-2 were treated with peginterferon alfa-2a 180 mcg/wk plus ribavirin 800 mg/d for 24 weeks and followed up for 24 weeks. The HCV RNA was qualitatively assessed after 4 weeks of treatment, and RVR was defined as undetectable HCV RNA at the 4th week. Retrospectively, 26 patients were treated with the standard treatment strategy (≥80% of the intended duration and dosage), 14 patients with a short-term treatment strategy (<80% intended duration and dosage) and 2 patients were excluded. Results: Among the 42 patients, 35 patients (83%) had RVR and 38 patients (90%) had a sustained virologic response (SVR). All 7 patients without RVR were treated with the standard treatment strategy, in whom 6 patients (86%) had SVR. Among the 35 patients with RVR, 14 patients were treated with short-term treatment and 19 patients were treated with the standard treatment. SVR was obtained in 12 out of the 14 patients (86%) in the short-term treatment group and 18 out of the 19 (95%) in the standard treatment group (P=0.373). Conclusion: HCV genotype-2 patients who have RVR with peginterferon and ribavirin treatment can be treated with a short-term treatment without compromising the chances for SVR. However, an additional trial will be needed to optimize the treatment duration. (Korean J Hepatol 2007;13:341-348)

Citations

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  • Efficacy and Tolerability of Peginterferon Alpha Plus Ribavirin in the Routine Daily Treatment of Chronic Hepatitis C Patients in Korea: A Multi-Center, Retrospective Observational Study
    Sang Hoon Park, Choong Kee Park, Jin Woo Lee, Young Seok Kim, Sook-Hyang Jeong, Yun Soo im, Ju Hyun Kim, Seong Gyu Hwang, Kyu Sung Rim, Hyung Joon Yim, Jae Youn Cheong, Sung Won Cho, June Sung Lee, Young Min Park, Jeong Won Jang Chun Kyon Lee, Joo Hyun Sh
    Gut and Liver.2012; 6(1): 98.     CrossRef
  • Treatment of Chronic Hepatitis C: Shorter Treatment Duration for Genotype 2 or 3 Infection
    Sook-Hyang Jeong
    The Korean Journal of Hepatology.2007; 13(3): 301.     CrossRef
  • 4,772 View
  • 21 Download
  • Crossref

Editorial

Treatment of Chronic Hepatitis C: Shorter Treatment Duration For Genotype 2 or 3 Infection
Sook Hyang Jeong
Korean J Hepatol 2007;13(3):301-303.
Published online September 20, 2007
DOI: https://doi.org/10.3350/kjhep.2007.13.3.301
  • 4,157 View
  • 20 Download

Original Articles

Efficacy of Combination of Interferon α 2a , Ribavirin and UDCA in the Treatment of Chronic Hepatitis C
Dong Jin Suh , Neung Hwa Park , Young Hwa Chung , Young Sang Lee
Korean J Hepatol 1998;4(2):109-119.
Background/Aims
- Although the only therapy of proven benefit for chronic hepatitis C is interferon alpha, the rate of sustained response after treatment with interferon is less than 25%. A 6-month course of combination therapy with interferon and ribavirin was associated with higher rate of long-term response than either interferon or ribavirin alone. Pilot studies suggested that combination of interferon and ursodeoxy-cholic acid (UDCA) resulted in higher biochemical response than interferon alone. We investigated the rates of end of treatment response(ETR) and sustained response(SR) of combination therapy of interferon e2a, ribavirin and UDCA and compared it with interferon a 2a alone. Methods' Ninty-five naive patients with chronic hepatitis C who have been positive for anti-HCV by 3rd generation EIA and HCV RNA by RT-PCR and had elevated level of ALT over 6 months were included. They were assigned to three groups. Thirty seven patients in group 1 were treated with interferon a 2a (3MU thrice weekly) in combination with ribavirin (600mg/day) and UDCA (600mg/day) for 6 months. Twenty nine patients in group 2 were treated with the same dose of interferon a 2a alone for 6 months. Changes of ALT and HCV RNA were observed over 12 months (average 3029 mos) after the end of treatment in both groups. Twenty nine patients in group 3 were observed over 12 months without antiviral treatment. HCV genotypes were tested by Innop-Lipa in 24 patients in group 1. Results- In group 1, not only ETR (68%) but also 12 month SR rate (54%) was significantly higher than group 2(31%, 21% respectively). There was no difference in relapse rate between two groups. The level of ALT became normalized and HCV RNA negative within 1 month after treatment in most responders in group l. Genotype 1b was associated with lower ETR and SR than non-lb, although not significant stastistically. Conclusion- Both the ETR and 12 month SR rate were significantly higher after combination treatment of interferon a 2a, ribavirin and UDCA than interferon e 2a alone in chronic hepatitis C. It is suggested that this combination is preferable to interferon alone in the treatment of naive patients with chronic hepatitis C. (Korean J Hepatol 1998;4:109 119)
  • 3,221 View
  • 14 Download
Recurrence and Management of Hepatitis C after Liver Transplantation
Ki Bong Oh, M.D., Sung Gyu Lee, M.D., Young Joo Lee, M.D., Kwang Min Park, M.D., Shin Hwang, M.D., Ki Hun Kim, M.D., Chul Soo Ahn, M.D., Deok Bog Moon, M.D., Chong Woo Chu, M.D., Hyun Seung Yang, M.D., Tae Yong Ha, M.D. and Sung Hoon Cho, M.D.
Korean J Hepatol 2003;9(3):180-187.
Background/Aims
End-stage liver disease caused by viral hepatitis C has been increasing recently in Korea. In this study, we investigated the clinical progress, recurrence, and management of hepatitis C patients who underwent liver transplantation, Methods: We retrospectively reviewed the clinical progress and management of 16 patients (2.7%) with hepatitis C among 587 liver transplant patients from August 1992 to August 2002. Results: Eleven cases among 16 patients were males. The median age was 56±6(42-62) years and the median follow-up period was 6±13 (1-41) months. Thirteen cases underwent living donor liver transplantation and three had cadaveric whole liver transplantation. Clinical recurrence occurred in nine cases (56.3%) and mean time of recurrence was 5.2 months, Histological recurrence cases were eight (50%). A positive result of HCV RNA PCR was found in 90.9%, and all cases of clinical and histological recurrence in groups in the same periods were PCR-positive. Among eight cases showing histological recurrence five patients were managed by ribavirin monotherapy, two patients received interferon and ribavirin combination therapy, and one patient was not treated at all, The serum serum aminotransferase level was normalized in six cases (75%) of them. Conclusions: We observed that the HCV reinfection rate of a transplanted liver was high in this study, as in other reports in the literature, The prevention of HCV recurrence and the management of post-recurrent cirrhotic change are crucial for graft and patient survival. We think customized protocols are needed for every situation of recurrent hepatitis C.(Korean J Hepatol 2003;9:180-187)
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Review

Peginterferon-alpha and Ribavirin Combination Therapy in Chronic Hepatitis C
Kwang Hyub Han , Young Hoon Yoon
Korean J Hepatol 2004;10(2):81-87.
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Original Article
Peginterferon Alfa-2a plus Ribavirin for Initial Treatment of Chronic Hepatitis C in Korea
Hyuk Lee, M.D., Moon Seok Choi, M.D., Seung Woon Paik, M.D., Jeong Hwan Kim, M.D., Do Young Kim, M.D., Joon Hyoek Lee, M.D., Kwang Cheol Koh, M.D., Byung Chul Yoo, M.D., Jong Chul Rhee, M.D. and Soon Mi Song, R.N.1
Korean J Hepatol 2006;12(1):31-40.
Background/Aims
Combination therapy with peginterferon and ribavirin is a standard therapy for western patients with chronic hepatitis C; however, its efficacy remains unclear in East Asian patients. We evaluated the efficacy and safety of administering peginterferon alfa-2a plus ribavirin in native Korean patients with chronic hepatitis C. Methods: Seventy-five patients with detectable HCV RNA (52.0% male, median age: 50.8 years) were eligible for the study. The patients were treated with peginterferon alfa-2a 180 mcg/week plus ribavirin 800 mg/day for 24 weeks (for genotype non-1, n=46) or 1000-1200 mg/day for 48 weeks (for genotype 1, n=29). The early virologic response (EVR), the end of treatment virologic response (ETVR), the sustained virologic response (SVR), the biochemical response and the adverse event were analyzed. Results: EVR was seen in 86.2% of the patients with genotype 1. The ETVR was 58.6% in the genotype 1 group and 84.8% in the genotype non-1 group (P=0.02). The overall SVR was 70.7%: 55.2% in the genotype 1 group and 80.4% in the non-1 group (P=0.04). The sustained biochemical response was 64.0%. Multivariate analysis showed that the baseline HCV RNA level (Odds ratio: 0.045, 95% CI: 0.011-0.183, P<0.001) and genotype (Odds ratio: 0.247, 95% CI: 0.063-0.969, P=0.045) had an independent effect on the SVR. Neutropenia, anemia, flu-like symptoms and itching were the common adverse events. Aggravated liver function led to discontinuation of therapy for six patients. Dose modification in twenty-nine patients was effective without producing a significant reduction of the SVR. Conclusions: Our data suggest that the efficacy of peginterferon plus ribavirin therapy in Koreans is comparable to those from studies on Western patients as an initial treatment for chronic hepatitis C patients. The baseline HCV RNA level and the genotype can be significant factors influencing the SVR. (Korean J Hepatol 2006;12:31-40)
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