Department of Internal Medicine III, Division of Gastroenterology and Hepatology, Medical University of Vienna, Vienna, Austria.
Department of Internal Medicine IV, Wilhelminenspital, Vienna, Austria.
Liver Int. 2018 Jun;38(6):1028-1035. doi: 10.1111/liv.13629. Epub 2017 Dec 1.
The introduction of direct-acting antivirals (DAA) has increased sustained virological response (SVR) rates in patients with advanced liver disease and chronic hepatitis C(CHC)infection. At present, data on clinical outcome and long-term durability of viral eradication after successful DAA therapy are scarce.
To evaluate the long-term success of viral eradication in patients with advanced fibrosis or cirrhosis treated with DAAs.
Five hundred and fifty-one patients with advanced fibrosis (n = 158) or cirrhosis (CPS-A:317,CPS-B/C:76) and SVR after interferon and ribavirin-free DAA therapy treated between October 2013 and April 2016 were studied with a median follow-up of 65.6 (13.0-155.3) weeks. Only patients without hepatocellular carcinoma (HCC) at baseline and without liver transplantation were included.
Twelve patients (2.2%) died during follow-up: the mortality rate was 0.6% in F3, 2.2% in CPS-A and 5.3% in CPS-B/C patients (P = .08). During follow-up 36 patients with cirrhosis (9.1%) developed a liver related event, including 16 with de-novo HCC (4.1%). Seven patients were transplanted at a median of 9.7 (range 3.8-21.7) months after EOT. History of decompensation was significantly associated with liver related events during follow-up (HR 7.9; 95% CI 2.7-22.6; P < .001), and with mortality (HR 5.5; 95% CI 1.5-20.2, P = .01).
Eradication of HCV by DAA therapy was durable irrespective of the DAA combination used. Most of the cured patients had an excellent long-term clinical prognosis. Nevertheless, the risk of new occurrence of HCC remains worrisome and thus regular surveillance is obligatory even after clinical stabilization and improvement of the patient.
直接作用抗病毒药物(DAA)的引入提高了晚期肝病和慢性丙型肝炎(CHC)感染患者的持续病毒学应答(SVR)率。目前,关于 DAA 治疗后成功清除病毒的临床结果和长期耐久性的数据仍然有限。
评估 DAA 治疗后患有晚期纤维化或肝硬化的患者病毒清除的长期效果。
对 2013 年 10 月至 2016 年 4 月期间接受干扰素和利巴韦林免费 DAA 治疗后获得 SVR 的 551 例晚期纤维化(n=158)或肝硬化(CPS-A:317 例,CPS-B/C:76 例)患者进行研究,中位随访时间为 65.6(13.0-155.3)周。仅纳入基线时无肝细胞癌(HCC)且未接受肝移植的患者。
12 例患者(2.2%)在随访期间死亡:F3 患者的死亡率为 0.6%,CPS-A 患者为 2.2%,CPS-B/C 患者为 5.3%(P=0.08)。随访期间,36 例肝硬化患者(9.1%)发生与肝脏相关的事件,包括 16 例新发 HCC(4.1%)。7 例患者在 EOT 后中位 9.7(范围 3.8-21.7)个月时进行了移植。失代偿病史与随访期间的肝脏相关事件显著相关(HR 7.9;95%CI 2.7-22.6;P<0.001),也与死亡率相关(HR 5.5;95%CI 1.5-20.2,P=0.01)。
DAA 治疗清除 HCV 是持久的,与所使用的 DAA 组合无关。大多数治愈的患者具有极好的长期临床预后。然而,新发生 HCC 的风险仍然令人担忧,因此即使在患者的临床稳定和改善后,仍需要进行定期监测。