Lee Shou-Wu, 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-Hue, Peng Cheng-Yuan, Yang Chi-Chieh, Chong Lee-Won, Huang Chien-Wei, Lin Chih-Wen, Chu Cheng-Hsin, Tsai Ming-Chang, Kao Jia-Horng, Liu Chun-Jen, Chuang Wan-Long, Lee Teng-Yu, Yu Ming-Lung
Division of Gastroenterology and Hepatology, Department of Internal Medicine, Taichung Veterans General Hospital, Taichung, Taiwan.
School of Medicine, Chung Shan Medical University, Taichung, Taiwan.
Clin Mol Hepatol. 2025 Jul;31(3):899-913. doi: 10.3350/cmh.2024.1015. Epub 2025 Feb 5.
BACKGROUND/AIMS: The survival benefit of direct-acting antiviral (DAA) therapy for hepatitis C virus (HCV) infection in patients with hepatocellular carcinoma (HCC), particularly in Barcelona Clinic Liver Cancer (BCLC) stages B/C, remains largely uncertain. We aimed to explore the impact of DAA therapy on overall survival (OS) in HCC patients using a nationwide cohort study.
We utilized the nationwide Taiwan Association for the Study of the Liver (TASL) HCV Registry (TACR) database to include all adults receiving a DAA therapy for HCV, excluding those with other viral infections, liver transplantation, non-HCC malignancies, and terminal-staged HCC. We respectively analyzed the adjusted odds ratio (aOR) for sustained virological response (SVR) and adjusted hazard ratio (aHR) for OS.
Between December 2013 and December 2020, 2,205 (9.3%) patients with HCC and 21,569 (90.7%) patients without HCC were include. The SVR rates were 96.6% in the HCC group and 98.8% in the non-HCC group (P<0.001), with HCC being an independent risk factor affecting SVR (aOR 0.41; 95% CI 0.31-0.54; P<0.001). In the whole patient cohort, SVR was independently associated with improved OS (aHR 0.46; 95% CI 0.35-0.60; P<0.001). Among patients with baseline HCC, SVR remained an independent factor related to OS (aHR 0.41; 95% CI 0.28-0.59; P<0.001). The impact of SVR on OS persisted significantly across BCLC stages 0/A and stages B/C.
High SVR rates among HCC patients underscore the importance of DAA therapy in enhancing OS, reaffirming its efficacy across various HCC stages.
背景/目的:直接抗病毒(DAA)疗法对肝细胞癌(HCC)患者丙型肝炎病毒(HCV)感染的生存获益,尤其是在巴塞罗那临床肝癌(BCLC)分期为B/C期的患者中,仍存在很大不确定性。我们旨在通过一项全国性队列研究,探讨DAA疗法对HCC患者总生存期(OS)的影响。
我们利用全国性的台湾肝脏研究学会(TASL)HCV注册数据库(TACR),纳入所有接受DAA治疗HCV的成年人,排除那些患有其他病毒感染、肝移植、非HCC恶性肿瘤和终末期HCC的患者。我们分别分析了持续病毒学应答(SVR)的调整优势比(aOR)和OS的调整风险比(aHR)。
在2013年12月至2020年12月期间,纳入了2205例(9.3%)HCC患者和21569例(90.7%)非HCC患者。HCC组的SVR率为96.6%,非HCC组为98.8%(P<0.001),HCC是影响SVR的独立危险因素(aOR 0.41;95%CI 0.31-0.54;P<0.001)。在整个患者队列中,SVR与OS改善独立相关(aHR 0.46;95%CI 0.35-0.60;P<0.001)。在基线为HCC的患者中,SVR仍然是与OS相关的独立因素(aHR 0.41;95%CI 0.28-0.59;P<0.001)。SVR对OS的影响在BCLC 0/A期和B/C期患者中均持续显著。
HCC患者的高SVR率凸显了DAA疗法对提高OS的重要性,再次证实了其在不同HCC分期中的疗效。