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直接作用抗病毒药物治疗的丙型肝炎相关肝硬化患者肝细胞癌的发生率。

Incidence of Hepatocellular Carcinoma in Patients With HCV-Associated Cirrhosis Treated With Direct-Acting Antiviral Agents.

机构信息

Sezione di Gastroenterologia e Epatologia, Dipartimento Biomedico di Medicina Interna e Specialistica (Di.Bi.M.I.S.), University of Palermo, Palermo, Italy.

UOC Epatologia Clinica e Biomolecolare and AOUP G Martino, Dipartimento di Medicina Interna e Sperimentale, University of Messina, Messina, Italy.

出版信息

Gastroenterology. 2018 Aug;155(2):411-421.e4. doi: 10.1053/j.gastro.2018.04.008. Epub 2018 Apr 12.

Abstract

BACKGROUND & AIMS: Studies have produced conflicting results of the incidence of hepatocellular carcinoma (HCC) in patients with hepatitis C virus-associated cirrhosis treated with direct-acting antivirals (DAAs). Data from clinics are needed to accurately assess the occurrence rate of HCC in patients with cirrhosis in the real world.

METHODS

We collected data from a large prospective study of 2,249 consecutive patients (mean age = 65.4 years, 56.9% male) with hepatitis C virus-associated cirrhosis (90.5% with Child-Pugh class A and 9.5% with Child-Pugh class B) treated with DAAs from March 2015 through July 2016 at 22 academic and community liver centers in Sicily, Italy. HCC occurrence was evaluated by Kaplan-Meier curves. Cox regression analysis was used to identify variables associated with HCC development.

RESULTS

A sustained virologic response (SVR) was achieved by 2,140 patients (total = 95.2%; 95.9% with Child Pugh class A and 88.3% with Child Pugh class B; P < .001). Seventy-eight patients (3.5%) developed HCC during a mean follow-up of 14 months (range = 6-24 months). At 1 year after exposure to DAAs, HCC developed in 2.1% of patients with Child-Pugh class A with an SVR and 6.6% of patients with no SVR and in 7.8% of patients with Child-Pugh class B with an SVR and 12.4% of patients with no SVR (P < .001 by log-rank test). Albumin level below 3.5 g/dL (hazard ratio = 1.77, 95% confidence interval = 1.12-2.82, P = .015), platelet count below 120 × 10/L (hazard ratio = 3.89, 95% confidence interval = 2.11-7.15, P < .001), and absence of an SVR (hazard ratio = 3.40, 95% confidence interval = 1.89-6.12, P < .001) were independently associated increased risk for HCC. The mean interval from exposure to DAAs to an HCC diagnosis was 9.8 months (range = 2-22 months) and did not differ significantly between patients with (n = 64, 9.2 months) and without (n = 14, 12.0 months) an SVR (P = .11). A larger proportion of patients with an SVR had a single HCC lesion (78% vs 50% without an SVR; P = .009) or an HCC lesion smaller than 3 cm (58% vs 28% without an SVR; P = .07).

CONCLUSIONS

In an analysis of data from a large prospective study of patients with hepatitis C virus-associated compensated or decompensated cirrhosis, we found that the SVR to DAA treatment decreased the incidence of HCC over a mean follow-up of 14 months.

摘要

背景与目的

已有研究对丙型肝炎病毒相关肝硬化患者接受直接作用抗病毒药物(DAA)治疗后肝细胞癌(HCC)的发病率得出了相互矛盾的结果。需要来自临床的数据来准确评估现实世界中肝硬化患者 HCC 的发生率。

方法

我们从意大利西西里岛 22 个学术和社区肝脏中心进行的一项关于 2249 例连续丙型肝炎病毒相关肝硬化患者(平均年龄 65.4 岁,56.9%为男性)的大型前瞻性研究中收集数据。这些患者在 2015 年 3 月至 2016 年 7 月期间接受了 DAA 治疗,90.5%的患者为 Child-Pugh 分级 A,9.5%的患者为 Child-Pugh 分级 B。通过 Kaplan-Meier 曲线评估 HCC 的发生情况。采用 Cox 回归分析鉴定与 HCC 发展相关的变量。

结果

2140 例患者(总数为 95.2%;Child-Pugh 分级 A 患者为 95.9%,Child-Pugh 分级 B 患者为 88.3%;P<.001)获得了持续病毒学应答(SVR)。在平均 14 个月(6-24 个月)的随访期间,78 例患者(3.5%)发展为 HCC。在接触 DAA 治疗后 1 年,Child-Pugh 分级 A 患者中 SVR 者 HCC 的发生率为 2.1%,无 SVR 者为 6.6%;Child-Pugh 分级 B 患者中 SVR 者为 7.8%,无 SVR 者为 12.4%(log-rank 检验 P<.001)。白蛋白水平<3.5 g/dL(危险比=1.77,95%置信区间=1.12-2.82,P=.015)、血小板计数<120×10/L(危险比=3.89,95%置信区间=2.11-7.15,P<.001)和无 SVR(危险比=3.40,95%置信区间=1.89-6.12,P<.001)与 HCC 风险增加独立相关。从接触 DAA 到 HCC 诊断的平均间隔时间为 9.8 个月(2-22 个月),在 SVR 患者(n=64,9.2 个月)和无 SVR 患者(n=14,12.0 个月)之间无显著差异(P=.11)。SVR 患者中更大多数患者具有单个 HCC 病变(78%比无 SVR 患者为 50%;P=.009)或 HCC 病变直径<3 cm(58%比无 SVR 患者为 28%;P=.07)。

结论

在对丙型肝炎病毒相关代偿或失代偿性肝硬化患者的大型前瞻性研究数据进行分析时,我们发现 DAA 治疗的 SVR 降低了平均随访 14 个月时 HCC 的发生率。

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