Department of Gastroenterology, Graduate School of Medicine, The University of Tokyo, Japan.
Department of Gastroenterology, Graduate School of Medicine, The University of Tokyo, Japan.
J Hepatol. 2019 Jan;70(1):78-86. doi: 10.1016/j.jhep.2018.09.029. Epub 2018 Oct 16.
BACKGROUND & AIMS: It remains controversial whether direct-acting antivirals (DAAs) accelerate the recurrence of hepatitis C-related hepatocellular carcinoma (HCC) after curative therapy. This study aimed to evaluate HCC recurrence after DAA treatment of chronic hepatitis C.
We enrolled patients with a history of successful radiofrequency ablation treatment for hepatitis C-related HCC who received antiviral therapy with DAAs (DAA group: 147 patients) or with interferon (IFN)-based therapy (IFN group: 156 patients). We assessed HCC recurrence rates from the initiation of antiviral therapy using the Kaplan-Meier method and evaluated risk factors for HCC recurrence by multivariate Cox proportional hazard regression analysis. The recurrence pattern was categorized as follows: intrahepatic recurrence with a single tumor <2 cm (stage 0), a single tumor or up to 3 tumors ≤3 cm (stage A), multinodular (stage B), and extrahepatic metastasis or macrovascular invasion (stage C).
The recurrence rates at 1 and 2 years were 39% and 61% in the IFN group and 39% and 60% in the DAA group, respectively (p = 0.43). Multivariate analysis identified higher lens culinaris agglutinin-reactive fraction of alpha-fetoprotein level, a history of multiple HCC treatments, and a shorter interval between HCC treatment and initiation of antiviral therapy as independent risk factors for HCC recurrence. HCC recurrence in stage 0, A, B, and C was found in 56 (41%), 60 (44%), 19 (14%), and 1 (0.7%) patients in the IFN group and 35 (44%), 32 (40%), 11 (14%), and 2 (2.5%) patients in the DAA group, respectively (p = 0.70).
HCC recurrence rates and patterns after initiation of antiviral therapy did not differ between patients who received IFN-based therapy and DAA therapy.
We detected no significant difference in early hepatocellular carcinoma (HCC) recurrence rates and patterns between patients who received interferon-based and direct-acting antiviral therapy after HCC treatment. High lens culinaris agglutinin-reactive fraction of alpha-fetoprotein level, short recurrence-free period, and a history of multiple HCC treatments were independent risk factors for early HCC recurrence after the initiation of antiviral therapy.
直接作用抗病毒药物(DAA)是否会加速丙型肝炎相关肝细胞癌(HCC)根治性治疗后的复发仍存在争议。本研究旨在评估 DAA 治疗慢性丙型肝炎后 HCC 的复发情况。
我们纳入了既往成功接受射频消融治疗丙型肝炎相关 HCC 并接受 DAA(DAA 组:147 例)或干扰素(IFN)为基础治疗(IFN 组:156 例)抗病毒治疗的患者。我们采用 Kaplan-Meier 法评估抗病毒治疗开始后 HCC 复发率,并通过多变量 Cox 比例风险回归分析评估 HCC 复发的危险因素。将复发模式分为以下几类:肝内单发肿瘤<2cm(0 期)、单发肿瘤或≤3 个肿瘤≤3cm(A 期)、多结节(B 期)和肝外转移或大血管侵犯(C 期)。
IFN 组和 DAA 组 1 年和 2 年的复发率分别为 39%和 61%(p=0.43)和 39%和 60%。多变量分析确定较高的甲胎蛋白岩藻糖基转移酶反应部分、多次 HCC 治疗史以及 HCC 治疗与抗病毒治疗开始之间的较短间隔为 HCC 复发的独立危险因素。IFN 组和 DAA 组中分别有 56 例(41%)、60 例(44%)、19 例(14%)和 1 例(0.7%)患者发生 0 期、A 期、B 期和 C 期 HCC 复发,35 例(44%)、32 例(40%)、11 例(14%)和 2 例(2.5%)患者发生 HCC 复发(p=0.70)。
接受 IFN 为基础治疗和 DAA 治疗的患者在开始抗病毒治疗后的 HCC 复发率和模式无显著差异。高甲胎蛋白岩藻糖基转移酶反应部分、较短的无复发间期和多次 HCC 治疗史是抗病毒治疗开始后 HCC 早期复发的独立危险因素。