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原发性或二级预防中 HCV 清除可优化肝细胞癌的治疗管理。

HCV Eradication in Primary or Secondary Prevention Optimizes Hepatocellular Carcinoma Curative Management.

机构信息

Service d'Hépatologie, Hôpital Avicenne, AP-HP, Bobigny, France.

Université Paris 13, Sorbonne Paris Cité, "Equipe labellisée Ligue Contre le Cancer", Saint-Denis, France.

出版信息

Cancer Prev Res (Phila). 2021 May;14(5):581-592. doi: 10.1158/1940-6207.CAPR-20-0465. Epub 2021 Feb 19.

Abstract

To assess the impact of HCV eradication on the outcomes of cirrhotic patients treated curatively for incidental hepatocellular carcinoma (HCC) detected during surveillance program. Data were collected on 1,323 French patients with compensated biopsy-proven HCV cirrhosis recruited in 35 centers (ANRS CO12 CirVir cohort). Sustained virologic responses (SVR) and the occurrence of HCC were recorded prospectively. During a median follow-up of 68.3 months, 218 patients developed HCC, 126 of whom underwent a curative procedure as first-line therapy (ablation = 95, resection = 31). The HCC BCLC stage was 0/A in 97.5% of patients; 74 (58.7%) never achieved SVR. During a median follow-up of 26.0 months after HCC treatment, 59 (46.8%) experienced HCC recurrence. SVR was not associated with a recurrence, whether considering final SVR status [HR = 0.77; 95% confidence interval (95% CI), 0.43-1.39; = 0.39] or its time to achievement (prior to/after HCC occurrence; global = 0.28). During the same timeframe, 46 patients with HCC (36.5%) died (liver failure: 41.9%, HCC progression: 37.2%, extrahepatic causes: 20.9%). Under multivariate analysis, SVR was associated with improved survival [HR = 0.21; 95% CI, 0.08-0.52; = 0.001]. Survival benefit was explained by a lower incidence of liver decompensation and higher rates of sequential HCC re-treatment. Direct antiviral intake was not associated with a higher risk of HCC recurrence, but with improved survival (HR = 0.23; 95% CI, 0.06-0.83; = 0.024). HCV eradication in primary or secondary prevention optimizes HCC management through preservation of liver function and improves survival, whatever the regimen. PREVENTION RELEVANCE: Liver failure is a competing risk of death in patients with HCC eligible for curative procedures. HCV eradication does not decrease risk of HCC recurrence in the first two years, but enables sequential curative HCC treatments through preservation of liver function. Direct-acting antiviral agent intake is not associated with HCC recurrence and improves survival.

摘要

评估 HCV 清除对接受治疗的偶然发现的 HCC 患者的结局的影响,这些患者在监测计划中被检测到患有肝硬化。研究数据来自于 35 个中心的 1323 名法国代偿性活检证实的 HCV 肝硬化患者(ANRS CO12 CirVir 队列)。记录持续病毒学应答(SVR)和 HCC 的发生情况。中位随访 68.3 个月期间,218 例患者发生 HCC,其中 126 例作为一线治疗(消融=95,切除=31)接受了根治性治疗。患者的 HCC BCLC 分期为 0/A 期占 97.5%;74 例(58.7%)从未达到 SVR。在 HCC 治疗后中位随访 26.0 个月时,59 例(46.8%)发生 HCC 复发。无论考虑最终 SVR 状态([HR=0.77;95%置信区间(95%CI),0.43-1.39; =0.39])或达到时间(在 HCC 发生之前/之后;总体[ =0.28]),SVR 均与复发无关。在此相同时间范围内,46 例 HCC 患者(36.5%)死亡(肝功能衰竭:41.9%,HCC 进展:37.2%,肝外原因:20.9%)。多变量分析显示,SVR 与改善的生存相关([HR=0.21;95%CI,0.08-0.52; =0.001])。生存获益归因于肝功能失代偿发生率降低和序贯 HCC 再治疗率提高。直接抗病毒药物摄入与 HCC 复发风险增加无关,但与改善的生存相关([HR=0.23;95%CI,0.06-0.83; =0.024])。原发性或二级预防中的 HCV 清除通过保护肝功能优化 HCC 管理,并改善生存,无论方案如何。预防相关性:对于有资格接受根治性治疗的 HCC 患者,肝功能衰竭是死亡的竞争风险。HCV 清除在最初两年内不会降低 HCC 复发的风险,但通过保护肝功能实现序贯根治性 HCC 治疗。直接作用抗病毒药物摄入与 HCC 复发无关,并且提高生存率。

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