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Comparison of the efficacy of sofosbuvir plus ribavirin in Chinese patients with genotype 3a or 3b HCV infection.
Huang, Rui; Rao, Huiying; Xie, Qing; Gao, Zhiliang; Li, Wu; Jiang, Deyuan; Mo, Hongmei; Massetto, Benedetta; Stamm, Luisa M; Brainard, Diana M; Wei, Lai.
  • Huang R; Peking University People's Hospital, Peking University Hepatology Institute, Beijing Key Laboratory for Hepatitis C and Immunotherapy for Liver Disease, Beijing, China.
  • Rao H; Peking University People's Hospital, Peking University Hepatology Institute, Beijing Key Laboratory for Hepatitis C and Immunotherapy for Liver Disease, Beijing, China.
  • Xie Q; Department of Infectious Disease, Rui Jin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
  • Gao Z; Infectious Disease Department, The Third Affiliated Hospital, Sun Yet-Sen University, Guangzhou, China.
  • Li W; First Affiliated Hospital of Kunming Medical University, Kunming, China.
  • Jiang D; Biostatistics, Gilead Sciences, Inc, Foster City, California.
  • Mo H; Biostatistics, Gilead Sciences, Inc, Foster City, California.
  • Massetto B; Virology, Gilead Sciences, Inc, Foster City, California.
  • Stamm LM; Biostatistics, Gilead Sciences, Inc, Foster City, California.
  • Brainard DM; Clinical Research, Gilead Sciences, Inc, Foster City, California.
  • Wei L; Biostatistics, Gilead Sciences, Inc, Foster City, California.
J Med Virol ; 91(7): 1313-1318, 2019 07.
Article en En | MEDLINE | ID: mdl-30861150
BACKGROUND AND AIM: Genotype 3b hepatitis C virus (HCV) infection represents approximately 50% of patients with genotype 3 in China. We compared the efficacy of sofosbuvir (SOF) plus ribavirin (RBV) in Chinese patients with genotype 3a and 3b HCV. METHODS: The analyzed data are from a phase 3, open-label study of SOF plus RBV for 24 weeks conducted in China. The primary endpoint for the trial was sustained virologic response at 12 weeks after the end of therapy (SVR12). RESULTS: Of 126 patients included in this analysis, 58 (46%) had genotype 3a and 68 (54%) had genotype 3b. Both the subtypes were similar in age, sex, body mass index, IL28B, and baseline HCV RNA. However, more treatment-experienced and cirrhotic patients were in the genotype 3b group. All 100% of patients with genotype 3a (95% confidence interval [CI], 94-100), and 91% (95% CI, 82-97) of patients with genotype 3b achieved SVR12 (P = 0.030). For treatment-experienced patients with genotype 3b, the SVR12 rate was 73% (95% CI, 39-94) and 88% (95% CI, 64-99) among patients with and without cirrhosis (P = 1.00), respectively. CONCLUSION: SOF plus RBV for 24 weeks in patients with HCV genotype 3 infection resulted in high rates of SVR. However, the SVR12 rate among patients with genotype 3b was lower than that observed in patients with genotype 3a infection, particularly among treatment-experienced patients with cirrhosis.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Antivirales / Ribavirina / Hepatitis C / Sofosbuvir Límite: Adult / Female / Humans / Male / Middle aged País como asunto: Asia Idioma: En Año: 2019 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Antivirales / Ribavirina / Hepatitis C / Sofosbuvir Límite: Adult / Female / Humans / Male / Middle aged País como asunto: Asia Idioma: En Año: 2019 Tipo del documento: Article