Effect of treatment periods on efficacy of glecaprevir and pibrentasvir in chronic hepatitis C: A nationwide, prospective, multicenter study

Background and aim In patients with chronic hepatitis C, 8 weeks of glecaprevir and pibrentasvir (GLE/PIB) treatment for chronic hepatitis (non‐cirrhosis) and 12 weeks for cirrhosis have been approved in Japan. However, whether 8 weeks of treatment for cirrhosis may reduce treatment efficacy has not...

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Published inJGH open Vol. 8; no. 4; pp. e13068 - n/a
Main Authors Morita, Atsuhiro, Tamaki, Nobuharu, Kobashi, Haruhiko, Mori, Nami, Tsuji, Keiji, Takaki, Shintaro, Hasebe, Chitomi, Akahane, Takehiro, Ochi, Hironori, Mashiba, Toshie, Urawa, Naohito, Fujii, Hideki, Mitsuda, Akeri, Kondo, Masahiko, Ogawa, Chikara, Uchida, Yasushi, Narita, Ryoichi, Marusawa, Hiroyuki, Kubotsu, Yoshihito, Matsushita, Tomomichi, Shigeno, Masaya, Yoshida, Hideo, Tanaka, Katsuaki, Okamoto, Eisuke, Kasai, Toyotaka, Ishii, Toru, Okada, Kazuhiko, Kurosaki, Masayuki, Izumi, Namiki
Format Journal Article
LanguageEnglish
Published Melbourne Wiley Publishing Asia Pty Ltd 01.04.2024
John Wiley & Sons, Inc
Wiley
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Summary:Background and aim In patients with chronic hepatitis C, 8 weeks of glecaprevir and pibrentasvir (GLE/PIB) treatment for chronic hepatitis (non‐cirrhosis) and 12 weeks for cirrhosis have been approved in Japan. However, whether 8 weeks of treatment for cirrhosis may reduce treatment efficacy has not been adequately investigated. Methods This prospective, nationwide, multicenter cohort study enrolled 1275 patients with chronic hepatitis C who received GLE/PIB therapy. The effect of liver fibrosis and treatment periods on the efficiency of GLE/PIB therapy was investigated. The primary endpoint was the sustained virological response (SVR) rate in patients with chronic hepatitis (non‐cirrhosis) and cirrhosis. The association between treatment periods and liver fibrosis on the SVR after 12 weeks of treatment rate was investigated. Results The SVR rates in patients with chronic hepatitis with 8 weeks of treatment, chronic hepatitis with 12 weeks of treatment, cirrhosis with 8 weeks of treatment, and cirrhosis with 12 weeks of treatment were 98.9% (800/809), 100% (87/87), 100% (166/166), and 99.1% (211/213), respectively, and were was not different among these groups (P = 0.4). Conclusion GLE/PIB therapy for chronic hepatitis C had high efficacy regardless of liver fibrosis status and treatment periods. Periods of GLE/PIB therapy could be chosen with available modalities, and high SVR rates could be achieved regardless of the decision. GLE/PIB therapy for chronic hepatitis C had high efficacy regardless of liver fibrosis status and treatment periods. Periods of GLE/PIB therapy could be chosen with available modalities, and high SVR rates could be achieved regardless of the decision.
Bibliography:Atsuhiro Morita, Nobuharu Tamaki and Haruhiko Kobashi contributed equally to this work.
Masayuki Kurosaki receives funding support from the Japan Agency for Medical Research and Development (JP23fk0210123h0001, 23fk0210113h0002) and the Japanese Ministry of Health, Welfare and Labor (23HC2001). Nobuharu Tamaki receives funding support from the Japan Agency for Medical Research and Development (JP23fk0210111h0002, JP23fk0210104s0202) and the Japanese Ministry of Health, Welfare and Labor (23HC2003, 23HC2002). Namiki Izumi receives funding support from the Japanese Ministry of Health, Welfare and Labor (grant number: 23HC2001).
Declaration of conflict of interest
Masayuki Kurosaki and Namiki Izumi have received lecture fees from AbbVie. The other authors have no conflicts of interest to declare.
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ISSN:2397-9070
2397-9070
DOI:10.1002/jgh3.13068