Long‐Term Outcomes of Sofosbuvir/Velpatasvir Treatment for Hepatitis C Virus‐Related Decompensated Cirrhosis: A Retrospective Multicenter Cohort Study

BACKGROUND: Sofosbuvir/velpatasvir (SOF/VEL) treatment for hepatitis C virus (HCV)-related decompensated cirrhosis has been shown to achieve a high sustained virologic response (SVR) rate and to improve liver function. However, limited data are available regarding the association between improvements in liver function and long-term survival. This multicenter study aimed to evaluate longitudinal changes in liver function and factors associated with long-term prognosis in patients treated with SOF/VEL. METHODS: Ninety-one patients who received SOF/VEL for HCV-related decompensated cirrhosis between March 2019 and December 2021 were enrolled. SVR rates, changes in Child-Pugh scores at 12, 24, 48, 72, and 120 weeks after treatment, changes in albumin-bilirubin (ALBI) scores, and overall survival (OS) were assessed. The impact of post-treatment ALBI improvement on prognosis was examined, and its predictive ability for 60-month OS was evaluated using receiver operating characteristic analysis. Survival was compared using the Kaplan-Meier method. RESULTS: The median age was 68.0 years; 36.3% of patients were male, and 24.2% had a history of hepatocellular carcinoma. SVR was achieved in 96.7% of patients. The median observation period was 57.0 months (IQR, 43.0-72.0), and 27 patients (29.7%) died during the observation period. Child-Pugh scores improved from the end of treatment and continued to improve; at 120 weeks, 55.9% of patients had scores of 5 or 6. The median OS was not reached, and the 5-year survival rate was 73.2%. ALBI improvement predicted 60-month OS with a sensitivity of 0.494, a specificity of 0.851, and an optimal cutoff value of a decrease in ALBI score of ≥ 0.103. Patients with ALBI improvement showed significantly better OS. CONCLUSIONS: SOF/VEL therapy achieved high SVR rates and demonstrated that post-treatment improvement in the ALBI score is strongly associated with a favorable long-term prognosis in patients with decompensated cirrhosis.

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Journal
Hepatology Research
Published
2026-04-01
DOI
https://doi.org/10.1111/hepr.70172
Primary Topic
Hepatitis C virus research
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article
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article

Long‐Term Outcomes of Sofosbuvir/Velpatasvir Treatment for Hepatitis C Virus‐Related Decompensated Cirrhosis: A Retrospective Multicenter Cohort Study

Yukimura Fukaya, Hiroki Tojima, Hidekazu Kurata, N. Morimoto et al.
Hepatology Research
Hepatitis C virus research
article

Long‐Term Outcomes of Sofosbuvir/Velpatasvir Treatment for Hepatitis C Virus‐Related Decompensated Cirrhosis: A Retrospective Multicenter Cohort Study

Yukimura Fukaya, Hiroki Tojima, Hidekazu Kurata, N. Morimoto, Yuki Kanayama, Kuniaki Fukuda, Takeshi Hatanaka, Keisuke Iizuka, Katsuhiko Horiuchi, Takahiro Arisaka, Satoshi Takakusagi, Takayoshi Suga, Toshiya Ohtake, Daichi Takizawa, Atsuko Soeda, Kouichi Miura, Toru Fukuchi, Y. Suzuki, Makoto Iijima, Takashi Hoshino, Shigeo Tano, Yuichi Majima, Toshiyuki Tahara, Toshiro Kamoshida, Yoshinari Takaoka, Shuichi Saito, Hitoshi Takagi, Liver Investigators in the Northern Kanto Study (LINKS) group, Hirotaka Arai, Yuichi Yamazaki, Shunji Watanabe, Takashi Ueno, Atsushi Naganuma, Masahiro Araki, Satoru Kakizaki, Tadashi Ikegami
article en

Abstract

BACKGROUND: Sofosbuvir/velpatasvir (SOF/VEL) treatment for hepatitis C virus (HCV)-related decompensated cirrhosis has been shown to achieve a high sustained virologic response (SVR) rate and to improve liver function. However, limited data are available regarding the association between improvements in liver function and long-term survival. This multicenter study aimed to evaluate longitudinal changes in liver function and factors associated with long-term prognosis in patients treated with SOF/VEL. METHODS: Ninety-one patients who received SOF/VEL for HCV-related decompensated cirrhosis between March 2019 and December 2021 were enrolled. SVR rates, changes in Child-Pugh scores at 12, 24, 48, 72, and 120 weeks after treatment, changes in albumin-bilirubin (ALBI) scores, and overall survival (OS) were assessed. The impact of post-treatment ALBI improvement on prognosis was examined, and its predictive ability for 60-month OS was evaluated using receiver operating characteristic analysis. Survival was compared using the Kaplan-Meier method. RESULTS: The median age was 68.0 years; 36.3% of patients were male, and 24.2% had a history of hepatocellular carcinoma. SVR was achieved in 96.7% of patients. The median observation period was 57.0 months (IQR, 43.0-72.0), and 27 patients (29.7%) died during the observation period. Child-Pugh scores improved from the end of treatment and continued to improve; at 120 weeks, 55.9% of patients had scores of 5 or 6. The median OS was not reached, and the 5-year survival rate was 73.2%. ALBI improvement predicted 60-month OS with a sensitivity of 0.494, a specificity of 0.851, and an optimal cutoff value of a decrease in ALBI score of ≥ 0.103. Patients with ALBI improvement showed significantly better OS. CONCLUSIONS: SOF/VEL therapy achieved high SVR rates and demonstrated that post-treatment improvement in the ALBI score is strongly associated with a favorable long-term prognosis in patients with decompensated cirrhosis.

Hepatology Research
Jichi Medical University (JP), Gunma University (JP), Fujitsu (Japan) (JP), Maebashi Red Cross Hospital (JP), Tsukuba Memorial Hospital (JP), Nagasaki Rousai Hospital (JP), Toyama City Hospital (JP), National Hospital Organization Takasaki Medical Center (JP), Tomita Hospital (JP), Sapporo Minami Hospital (JP), Koga Hospital (JP), Sapporo Kosei General Hospital (JP), Japanese Red Cross Kochi Hospital (JP), Saiseikai Utsunomiya hospital (JP), Gunma Saiseikai Maebashi Hospital (JP), Tokyo Medical University Ibaraki Medical Center (JP), National Institute of Technology, Oyama College (JP), Ibaraki Prefectural Central Hospital (JP), Gunma Chuo Hospital (JP), Hitachi General Hospital (JP), Isesaki Fukushima Hospital (JP), Tochigi Medical Center (JP), Dokkyo Medical University (JP)
Good health and well-being
Openalex Percentile: Top 40%
Hepatitis C virus research
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