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  4. Survival impact of hepatitis C virus eradication in patients with or without active hepatocellular carcinoma: A nationwide cohort study.
 
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Survival impact of hepatitis C virus eradication in patients with or without active hepatocellular carcinoma: A nationwide cohort study.

Journal
European journal of cancer (Oxford, England : 1990)
Journal Volume
232
Start Page
116109
ISSN
1879-0852
Date Issued
2026-01
Author(s)
Lee, Teng-Yu
Yang, Sheng-Shun
Tsai, Pei-Chien
Huang, Chung-Feng
Chen, Chi-Yi
Hung, Chao-Hung
Chen, Chien-Hung
Tai, Chi-Ming
Cheng, Pin-Nan
Kuo, Hsing-Tao
Tseng, Kuo-Chih
Mo, Lein-Ray
Lo, Ching-Chu
Huang, Yi-Hsiang
Lin, Han-Chieh
Lee, Pei-Lun
Bair, Ming-Jong
Chang, Te-Sheng
Lin, Chun-Yen
Wang, Szu-Jen
Hsieh, Tsai-Yuan
Yang, Tzeng-Huey
Peng, Cheng-Yuan
Yang, Chi-Chieh
Chong, Lee-Won
Huang, Chien-Wei
Lin, Chih-Wen
Chu, Cheng-Hsin
Tsai, Ming-Chang
JIA-HORNG KAO  
CHUN-JEN LIU  
Chuang, Wan-Long
Lee, Shou-Wu
Yu, Ming-Lung
DOI
10.1016/j.ejca.2025.116109
URI
https://scholars.lib.ntu.edu.tw/handle/123456789/736994
Abstract
Background: The survival benefit of direct-acting antiviral (DAA) in hepatitis C virus (HCV)-infected patients with or without active hepatocellular carcinoma (HCC) remains debated. This study aimed to clarify this issue. Methods: This retrospective nationwide cohort study utilized data from the Taiwan Association for the Study of the Liver (TASL) HCV Registry (TACR) to identify adults with HCC who received DAA therapy for HCV between December 2013 and December 2020. Patients with other viral infections, prior liver transplantation, non-HCC malignancies, or terminal-stage HCC were excluded. The primary outcome was overall survival (OS). The adjusted odds ratio (aOR) for sustained virological response (SVR) and the adjusted hazard ratio (aHR) for OS were calculated. Findings: A total of 2205 patients were included: 1771 (80.3 %) without active HCC and 434 (19.7 %) with active HCC. SVR was independently associated with improved OS (aHR 0.45, 95 % CI: 0.31-0.66; p < 0.001). In Barcelona Clinic Liver Cancer (BCLC) stage 0/A, the 3-year OS rate was significantly higher in the SVR group amongst patients with active HCC (71.7 %, 95 % CI 64.6-77.7 % vs. 39.9 %, 95 % CI 15.6-63.5 %; p = 0.007) but non-significantly higher amongst those without active HCC (84.2 %, 95 % CI 81.7-86.4 % vs. 70.0 %, 95 % CI 44.2-85.6 %; p = 0.181). In BCLC stage B/C, the 3-year OS rate was significantly higher in the SVR group amongst patients without active HCC (76.2 %, 95 % CI 70.2-81.2 % vs. 24.7 %, 95 % CI 5.3-51.3 %; p < 0.001) but not amongst those with active HCC (58.6 %, 95 % CI 47.9-67.7 % vs. 57.1 %, 95 % CI 17.2-83.7 %; p = 0.922). Conclusion: For BCLC stage 0/A HCC, early DAA initiation is recommended, even with active HCC. In BCLC stage B/C, DAA therapy appears most beneficial after tumor control.
Subjects
Chronic hepatitis C
Eradication
Liver cancer
Sustained virological response
Type
journal article

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