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首页> 外文期刊>Journal of Hepatology: The Journal of the European Association for the Study of the Liver >Direct-acting antivirals after successful treatment of early hepatocellular carcinoma improve survival in HCV-cirrhotic patients
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Direct-acting antivirals after successful treatment of early hepatocellular carcinoma improve survival in HCV-cirrhotic patients

机译:成功治疗早期肝细胞癌后的直接作用抗病毒药物改善HCV - 肝硬化患者的存活

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摘要

Background & Aims: The effectiveness of direct-acting antivirals (DAAs) against hepatitis C virus (HCV), following successful treatment of early hepatocellular carcinoma (HCC), has been studied extensively. However, the benefit in terms of overall survival (OS) remains to be conclusively demonstrated. The aim of this study was to assess the impact of DAAs on OS, HCC recurrence, and hepatic decompensation. Methods: We prospectively enrolled 163 consecutive patients with HCV-related cirrhosis and a first diagnosis of early Barcelona Clinic Liver Cancer stage 0/A HCC, who had achieved a complete radiologic response after curative resection or ablation and were subsequently treated with DAAs. DAA-untreated patients from the ITA.LI.CA. cohort (n = 328) served as controls. After propensity score matching, outcomes of 102 DAA-treated (DAA group) and 102 DAA-untreated patients (No DAA group) were compared. Results: In the DAA group, 7/102 patients (6.9%) died, HCC recurred in 28/102 patients (27.5%) and hepatic decompensation occurred in 6/102 patients (5.9%), after a mean follow-up of 21.4 months. OS was significantly higher in the DAA group compared to the No DAA group (hazard ratio [HR] 0.39; 95% CI 0.17-0.91; p = 0.03). HCC recurrence was not significantly different between the DAA and No DAA groups (HR0.70; 95% CI 0.44-1.13; p = 0.15). A significant reduction in the rate of hepatic decompensation was observed in the DAA group compared with the No DAA group (HR0.32; 95% CI 0.13-0.84; p = 0.02). In the DAA group, sustained virologic response was a significant predictor of OS (HR 0.02; 95% CI 0.00-0.19; p O.001), HCC recurrence (HR 0.25; 95% CI 0.11-0.57; p <0.001) and hepatic decompensation (HR 0.12; 95% CI 0.02-0.38; p = 0.02). Conclusions: In patients with HCV-related cirrhosis who had been successfully treated for early HCC, DAAs significantly improved OS compared with No DAA treatment. Lay summary: We aimed to determine whether direct-acting antivirals (DAAs) significantly improve overall survival in patients with hepatitis C virus-related compensated cirrhosis and a first diagnosis of hepatocellular carcinoma (HCC) which has been successfully treated with curative resection or ablation. Using propensity-score matched patients, we found that DAAs improved overall survival and reduced the risk of hepatic decompensation. However, the risk of HCC recurrence was not significantly reduced.
机译:背景&AIMS:在成功治疗早期肝细胞癌(HCC)之后,已经研究了直接作用抗病毒(DAAS)对丙型肝炎病毒(HCV)的有效性已经过度研究了早期肝细胞癌(HCC)。但是,在整体生存(OS)方面的好处仍有待地证明。本研究的目的是评估DAAs对OS,HCC复发和肝脏失代偿的影响。方法:我们宣传163名患有HCV相关肝癌的163名患者,并于早期的巴塞罗那临床肝癌阶段0 / HCC诊断,他在治疗切除或消融后达到了完整的放射学反应,随后用DAA治疗。来自ITA.LI.ca的DAA-未经治疗的患者。队列(n = 328)作为对照。在倾倾匹配之后,比较了102种治疗(DAA组)和102个DAA-未处理患者(NOA组)的结果。结果:在DAA组,7/102患者(6.9%)死亡,HCC在28/102名患者中重复(27.5%)和肝脏失代偿发生在6/102名患者(5.9%)后,平均随访21.4几个月。与NO DAA组(危险比[HR] 0.39; 95%CI 0.17-0.91; P = 0.03)相比,DAA组在DAA组中显着高。 DAA和NOA组之间的HCC再次发生在DAA和NOA组之间没有显着差异(HR0.70; 95%CI 0.44-1.13; P = 0.15)。与NOA组(HR0.32; 95%CI 0.13-0.84; P = 0.02),在DAA组中观察到DAA组中肝脏失代偿速率显着降低。在DAA组中,持续的病毒学反应是OS的显着预测因子(HR 0.02; 95%CI 0.00-0.19; P O.001),HCC复发(HR 0.25; 95%CI 0.11-0.57; P <0.001)和肝失代偿(HR 0.12; 95%CI 0.02-0.38; p = 0.02)。结论:患有HCV相关肝硬化的患者已成功治疗HCC早期治疗,DAAS与无DAA治疗相比明显改善。 LAD总结:我们的目标是确定直接抗病毒率(DAAs)是否显着提高丙型肝炎病毒相关补偿肝硬化患者的整体生存率,以及肝细胞癌(HCC)的第一次诊断,该肝癌(HCC)已成功地治疗治疗切除或消融治疗。使用倾向评分匹配患者,我们发现DAAS改善了整体存活率并降低了肝脏失代偿的风险。然而,HCC复发的风险没有显着减少。

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