Section of Gastroenterology and Hepatology, Dipartimento di Promozione della Salute, Materno Infantile, Medicina Interna e Specialistica di Eccellenza (PROMISE), University of Palermo, Italy.
UOC Epatologia Clinica e Biomolecolare; AOUP G. Martino, Dipartimento di Medicina Interna e Sperimentale, University of Messina, Italy.
J Hepatol. 2019 Aug;71(2):265-273. doi: 10.1016/j.jhep.2019.03.027. Epub 2019 Apr 6.
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.
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.
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% CI0.17-0.91; p = 0.03). HCC recurrence was not significantly different between the DAA and No DAA groups (HR0.70; 95% CI0.44-1.13; 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% CI0.13-0.84; 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 <0.001), 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).
In patients with HCV-related cirrhosis who had been successfully treated for early HCC, DAAs significantly improved OS compared with No DAA treatment.
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.
已广泛研究过直接作用抗病毒药物(DAAs)在成功治疗早期肝细胞癌(HCC)后对丙型肝炎病毒(HCV)的疗效。然而,其对总体生存(OS)的获益仍有待明确证实。本研究旨在评估 DAA 对 OS、HCC 复发和肝失代偿的影响。
我们前瞻性纳入了 163 例 HCV 相关肝硬化且初诊为巴塞罗那临床肝癌 0/A 期的患者,这些患者在根治性切除或消融后获得完全影像学反应,随后接受 DAA 治疗。来自 ITA.LI.CA.队列的未接受 DAA 治疗的患者(n=328)作为对照组。经倾向评分匹配后,比较了 102 例接受 DAA 治疗的(DAA 组)和 102 例未接受 DAA 治疗的患者(无 DAA 组)的结局。
在 DAA 组中,7/102 例患者(6.9%)死亡,28/102 例患者(27.5%)HCC 复发,6/102 例患者(5.9%)发生肝失代偿,中位随访时间为 21.4 个月。与无 DAA 组相比,DAA 组的 OS 显著更高(风险比 [HR]0.39;95%CI0.17-0.91;p=0.03)。DAA 组和无 DAA 组 HCC 复发率无显著差异(HR0.70;95%CI0.44-1.13;p=0.15)。与无 DAA 组相比,DAA 组的肝失代偿发生率显著降低(HR0.32;95%CI0.13-0.84;p=0.02)。在 DAA 组中,持续病毒学应答是 OS(HR0.02;95%CI0.00-0.19;p<0.001)、HCC 复发(HR0.25;95%CI0.11-0.57;p<0.001)和肝失代偿(HR0.12;95%CI0.02-0.38;p=0.02)的显著预测因素。
在成功治疗早期 HCC 的 HCV 相关肝硬化患者中,与无 DAA 治疗相比,DAA 显著改善了 OS。
我们旨在确定直接作用抗病毒药物(DAAs)是否能显著改善丙型肝炎病毒相关代偿性肝硬化和首次诊断为肝细胞癌(HCC)且已成功接受根治性切除或消融治疗的患者的总体生存率。通过使用倾向评分匹配的患者,我们发现 DAA 可改善总体生存率并降低肝失代偿的风险。然而,HCC 复发的风险并未显著降低。