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Real-world Effectiveness and Tolerability of Interferon-free Direct-acting Antiviral for 15,849 Patients with Chronic Hepatitis C: A Multinational Cohort Study.
Ji, Fanpu; Tran, Sally; Ogawa, Eiichi; Huang, Chung-Feng; Suzuki, Takanori; Wong, Yu Jun; Toyoda, Hidenori; Jun, Dae Won; Li, Liu; Uojima, Haruki; Nozaki, Akito; Chuma, Makoto; Tseng, Cheng-Hao; Hsu, Yao-Chun; Ishigami, Masatoshi; Honda, Takashi; Atsukawa, Masanori; Haga, Hiroaki; Enomoto, Masaru; Trinh, Huy; Preda, Carmen Monica; Vutien, Phillip; Landis, Charles; Lee, Dong Hyun; Watanabe, Tsunamasa; Takahashi, Hirokazu; Abe, Hiroshi; Asai, Akira; Eguchi, Yuichiro; Li, Jie; Wang, Xiaozhong; Li, Jia; Liu, Junping; Liang, Jing; Lam, Carla Pui-Mei; Huang, Rui; Ye, Qing; Pan, Hongying; Zhang, Jiajie; Cai, Dachuan; Wang, Qi; Huang, Daniel Q; Wong, Grace; Wong, Vincent Wai-Sun; Li, Junyi; Do, Son; Furusyo, Norihiro; Nakamuta, Makoto; Nomura, Hideyuki; Kajiwara, Eiji.
Afiliação
  • Ji F; Department of Infectious Diseases, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi, China.
  • Tran S; Division of Gastroenterology and Hepatology, Department of Medicine, Stanford University Medical Center, Palo Alto, CA, USA.
  • Ogawa E; Department of General Internal Medicine, Kyushu University Hospital, Fukuoka, Japan.
  • Huang CF; Hepatobiliary Division, Department of Internal Medicine, Kaohsiung Medical University Hospital, Kaohsiung.
  • Suzuki T; Hepatitis Research Center, College of Medicine and Center for Liquid Biopsy and Cohort Research, Kaohsiung Medical University, Kaohsiung.
  • Wong YJ; Department of Gastroenterology and Metabolism, Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.
  • Toyoda H; Gastroenterology & Hepatology, Changi General Hospital, Singhealth, Singapore.
  • Jun DW; Singhealth Duke-NUS Medicine Academic Clinical Program, Singapore.
  • Li L; Department of Gastroenterology, Ogaki Municipal Hospital, Ogaki, Japan.
  • Uojima H; Department of Internal Medicine, Hanyang University, College of Medicine, Seoul, Korea.
  • Nozaki A; Hanyang Institute of Bioscience and Biotechnology, Hanyang University, Seoul, Korea.
  • Chuma M; Department of Hepatology, The Third People's Hospital of Kunming City, Kunming, Yunnan, China.
  • Tseng CH; Department of Gastroenterology, Internal Medicine, Kitasato University School of Medicine, Sagamihara, Japan.
  • Hsu YC; Gastroenterological Center, Yokohama City University Medical Center, Yokohama, Japan.
  • Ishigami M; Gastroenterological Center, Yokohama City University Medical Center, Yokohama, Japan.
  • Honda T; Division of Gastroenterology and Hepatology, Department of Internal Medicine, E-Da Cancer Hospital, Kaohsiung.
  • Atsukawa M; Division of Gastroenterology and Hepatology, Department of Internal Medicine, E-Da Cancer Hospital, Kaohsiung.
  • Haga H; Department of Gastroenterology and Hepatology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Enomoto M; Department of Gastroenterology and Hepatology, Nagoya University Graduate School of Medicine, Nagoya, Japan.
  • Trinh H; Division of Gastroenterology and Hepatology, Nippon Medical School, Tokyo, Japan.
  • Preda CM; Department of Gastroenterology, Yamagata University Faculty of Medicine, Yamagata, Japan.
  • Vutien P; Department of Transfusion Medicine and Department of Hepatology, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan.
  • Landis C; San Jose Gastroenterology, San Jose, CA, USA.
  • Lee DH; Gastroenterology & Hepatology Department, Clinic Fundeni Institute, Bucharest, Romania.
  • Watanabe T; Division of Gastroenterology and Hepatology, University of Washington, Seattle, WA, USA.
  • Takahashi H; Division of Gastroenterology and Hepatology, University of Washington, Seattle, WA, USA.
  • Abe H; Department of Gastroenterology, Good Gang-An Hospital, Busan, Korea.
  • Asai A; Division of Gastroenterology and Hepatology, St. Marianna University School of Medicine, Kawasaki, Japan.
  • Eguchi Y; Liver Center, Saga University Hospital, Saga, Japan.
  • Li J; Division of Metabolism and Endocrinology, Saga University Faculty of Medicine, Saga, Japan.
  • Wang X; Division of Gastroenterology and Hepatology, Shinmatsudo Central General Hospital, Chiba, Japan.
  • Li J; 2nd Department of Internal Medicine, Osaka Medical and Pharmaceutical University, Osaka, Japan.
  • Liu J; Liver Center, Saga University Hospital, Saga, Japan.
  • Liang J; Locomedical General Institute, Locomedical Eguchi Hospital, Saga, Japan.
  • Lam CP; Department of Infectious Diseases, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, Jiangsu, China.
  • Huang R; Affiliated Traditional Chinese Medicine Hospital of Xinjiang Medical University, Urumqi, Xinjiang, China.
  • Ye Q; Department of Gastroenterology and Hepatology, The Second People's Hospital of Tianjin, Tianjin, China.
  • Pan H; Department of Infectious Diseases, Henan Provincial People's Hospital Affiliated to Zhengzhou University, Zhengzhou, Henan, China.
  • Zhang J; Department of Gastroenterology and Hepatology, The Third Central Hospital of Tianjin, Tianjin, China.
  • Cai D; Department of Medicine, The University of Hong Kong, Hong Kong, China.
  • Wang Q; Department of Infectious Diseases, Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University, Nanjing, Jiangsu, China.
  • Huang DQ; Department of Gastroenterology and Hepatology, The Third Central Hospital of Tianjin, Tianjin, China.
  • Wong G; Department of Hepatology, Zhejiang Provincial People's Hospital Affiliated to Zhejiang University, Hangzhou, Zhejiang, China.
  • Wong VW; Department of Hepatology, Zhejiang Provincial People's Hospital Affiliated to Zhejiang University, Hangzhou, Zhejiang, China.
  • Li J; Department of Infectious Diseases, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, China.
  • Do S; Center of liver diseases, Beijing Ditan Hospital Affiliated to Capital Medical University, Beijing, China.
  • Furusyo N; Division of Gastroenterology and Hepatology, National University Hospital, Singapore.
  • Nakamuta M; Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
  • Nomura H; Department of Medicine and Therapeutics, The Chinese University of Hong Kong, Hong Kong, China.
  • Kajiwara E; State Key Laboratory of Digestive Disease, The Chinese University of Hong Kong, Hong Kong, China.
J Clin Transl Hepatol ; 12(7): 646-658, 2024 Jul 28.
Article em En | MEDLINE | ID: mdl-38993510
ABSTRACT
Background and

Aims:

As practice patterns and hepatitis C virus (HCV) genotypes (GT) vary geographically, a global real-world study from both East and West covering all GTs can help inform practice policy toward the 2030 HCV elimination goal. This study aimed to assess the effectiveness and tolerability of DAA treatment in routine clinical practice in a multinational cohort for patients infected with all HCV GTs, focusing on GT3 and GT6.

Methods:

We analyzed the sustained virological response (SVR12) of 15,849 chronic hepatitis C patients from 39 Real-World Evidence from the Asia Liver Consortium for HCV clinical sites in Asia Pacific, North America, and Europe between 07/01/2014-07/01/2021.

Results:

The mean age was 62±13 years, with 49.6% male. The demographic breakdown was 91.1% Asian (52.9% Japanese, 25.7% Chinese/Taiwanese, 5.4% Korean, 3.3% Malaysian, and 2.9% Vietnamese), 6.4% White, 1.3% Hispanic/Latino, and 1% Black/African-American. Additionally, 34.8% had cirrhosis, 8.6% had hepatocellular carcinoma (HCC), and 24.9% were treatment-experienced (20.7% with interferon, 4.3% with direct-acting antivirals). The largest group was GT1 (10,246 [64.6%]), followed by GT2 (3,686 [23.2%]), GT3 (1,151 [7.2%]), GT6 (457 [2.8%]), GT4 (47 [0.3%]), GT5 (1 [0.006%]), and untyped GTs (261 [1.6%]). The overall SVR12 was 96.9%, with rates over 95% for GT1/2/3/6 but 91.5% for GT4. SVR12 for GT3 was 95.1% overall, 98.2% for GT3a, and 94.0% for GT3b. SVR12 was 98.3% overall for GT6, lower for patients with cirrhosis and treatment-experienced (TE) (93.8%) but ≥97.5% for treatment-naive patients regardless of cirrhosis status. On multivariable analysis, advanced age, prior treatment failure, cirrhosis, active HCC, and GT3/4 were independent predictors of lower SVR12, while being Asian was a significant predictor of achieving SVR12.

Conclusions:

In this diverse multinational real-world cohort of patients with various GTs, the overall cure rate was 96.9%, despite large numbers of patients with cirrhosis, HCC, TE, and GT3/6. SVR12 for GT3/6 with cirrhosis and TE was lower but still excellent (>91%).
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article