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Erschienen in: Hepatology International 3/2023

27.03.2023 | Original Article

Effectiveness and safety of 8-week glecaprevir/pibrentasvir in HCV treatment-naïve patients with compensated cirrhosis: real-world experience from Taiwan nationwide HCV registry

verfasst von: Te-Sheng Chang, Chung-Feng Huang, Hsing-Tao Kuo, Ching-Chu Lo, Chien-Wei Huang, Lee-Won Chong, Pin-Nan Cheng, Ming-Lun Yeh, Cheng-Yuan Peng, Chien-Yu Cheng, Jee-Fu Huang, Ming-Jong Bair, Chih-Lang Lin, Chi-Chieh Yang, Szu-Jen Wang, Tsai-Yuan Hsieh, Tzong-Hsi Lee, Pei-Lun Lee, Wen-Chih Wu, Chih-Lin Lin, Wei-Wen Su, Sheng-Shun Yang, Chia-Chi Wang, Jui-Ting Hu, Lein-Ray Mo, Chun-Ting Chen, Yi-Hsiang Huang, Chun-Chao Chang, Chia-Sheng Huang, Guei-Ying Chen, Chien-Neng Kao, Chi-Ming Tai, Chun-Jen Liu, Mei-Hsuan Lee, Pei-Chien Tsai, Chia-Yen Dai, Jia-Horng Kao, Han-Chieh Lin, Wang-Long Chuang, Chi-Yi Chen, Kuo-Chih Tseng, Chao-Hung Hung, Ming-Lung Yu

Erschienen in: Hepatology International | Ausgabe 3/2023

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Abstract

Background

Large-scale real-world data of the 8-week glecaprevir/pibrentasvir (GLE/PIB) therapy for treatment-naïve patients of chronic hepatitis C virus (HCV) infection with compensated cirrhosis is scarce.

Methods

The TASL HCV Registry (TACR) is an ongoing nationwide registry program that aims to set up a database and biobank of patients with chronic HCV infection in Taiwan. In this study, data were analyzed as of 31 October 2021 for treatment-naïve HCV patients with compensated cirrhosis receiving 8-week GLE/PIB therapy. Effectiveness reported as sustained virologic response at off-therapy week 12 (SVR12) and safety profiles were assessed. Patient characteristics potentially related to SVR12 were also evaluated.

Results

Of the 301 patients enrolled, 275 had available SVR12 data. The SVR12 rate was 98.2% (270/275) in the modified intention-to-treat (mITT) population and 89.7% (270/301) in the ITT population. For those mITT patients with genotype 3, FibroScan > 20 kPa, platelet < 150,000/µl, and FibroScan > 20 kPa and platelet < 150,000/µl, the SVR12 rates were 100% (6/6), 100% (12/12), 98.0% (144/147), 100% (7/7), respectively. Overall, 24.9% (75/301) patients experienced adverse events (AEs). The most frequent AEs (> 5%) included fatigue (9.0%) and pruritus (7.0%). Seven (2.3%) patients experienced serious AEs and two (0.7%) resulted in permanent drug discontinuation. None of them were considered as GLE/PIB-related.

Conclusions

In this large-scale real-world Taiwanese cohort, 8-week GLE/PIB therapy was efficacious and well tolerated for treatment-naïve compensated cirrhosis patients. SVR12 rates were similarly high as in the clinical trials, including those with characteristics of advanced liver disease.
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Metadaten
Titel
Effectiveness and safety of 8-week glecaprevir/pibrentasvir in HCV treatment-naïve patients with compensated cirrhosis: real-world experience from Taiwan nationwide HCV registry
verfasst von
Te-Sheng Chang
Chung-Feng Huang
Hsing-Tao Kuo
Ching-Chu Lo
Chien-Wei Huang
Lee-Won Chong
Pin-Nan Cheng
Ming-Lun Yeh
Cheng-Yuan Peng
Chien-Yu Cheng
Jee-Fu Huang
Ming-Jong Bair
Chih-Lang Lin
Chi-Chieh Yang
Szu-Jen Wang
Tsai-Yuan Hsieh
Tzong-Hsi Lee
Pei-Lun Lee
Wen-Chih Wu
Chih-Lin Lin
Wei-Wen Su
Sheng-Shun Yang
Chia-Chi Wang
Jui-Ting Hu
Lein-Ray Mo
Chun-Ting Chen
Yi-Hsiang Huang
Chun-Chao Chang
Chia-Sheng Huang
Guei-Ying Chen
Chien-Neng Kao
Chi-Ming Tai
Chun-Jen Liu
Mei-Hsuan Lee
Pei-Chien Tsai
Chia-Yen Dai
Jia-Horng Kao
Han-Chieh Lin
Wang-Long Chuang
Chi-Yi Chen
Kuo-Chih Tseng
Chao-Hung Hung
Ming-Lung Yu
Publikationsdatum
27.03.2023
Verlag
Springer India
Erschienen in
Hepatology International / Ausgabe 3/2023
Print ISSN: 1936-0533
Elektronische ISSN: 1936-0541
DOI
https://doi.org/10.1007/s12072-023-10506-z

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