Sections of Gastroenterology and Hepatology and Health Services Research, Michael E. DeBakey Veterans Affairs Medical Center and Baylor College of Medicine, 2002 Holcombe Blvd. (MS152), Houston, TX, 77030, USA.
Center of Innovation, Effectiveness and Quality, Michael E. DeBakey Veterans Affairs Medical Center and Baylor College of Medicine, Houston, TX, USA.
Dig Dis Sci. 2019 Nov;64(11):3328-3336. doi: 10.1007/s10620-019-05641-3. Epub 2019 Apr 30.
With advent of direct-acting antiviral agents (DAA), hepatitis C virus (HCV) treatment is dramatically increasing. Although few studies reported rates of hepatocellular carcinoma (HCC) recurrence following DAA treatment, there have been no studies that followed sufficient number of DAA-treated patients after successful HCC treatment to examine HCC recurrence.
We conducted a cohort study of HCV+ patients who had successfully treated HCC before initiating DAAs. We conducted medical record reviews to confirm HCC diagnosis, treatment, and remission prior to DAA initiation, and subsequent HCC recurrence. We calculated HCC recurrence rate and examined the recurrent tumor characteristics. We used Cox proportional hazard model to identify factors associated with HCC recurrence.
We identified 264 HCV+ patients who received DAAs after an average of 30.9 (20.6) months following HCC treatment. HCC recurred in 26.1% patients during 23.3 (9.8) months follow-up, at a rate of 0.38 [0.30, 0.48] per 1000 person-month. Most (82.3%) recurrent HCC were early stage. Receiving non-curative treatment for HCC was associated with a higher risk of recurrence than curative treatment (HR = 2.06, [1.24, 3.40]). The risk of HCC recurrence decreased with longer duration between HCC treatment completion and DAA initiation (HR = 0.97, [0.95, 0.99] per additional month). Compared with patients who achieved sustained virological response (SVR), those without SVR had significantly increased risk of HCC recurrence (HR = 4.17, [1.48, 11.75]).
We conclude that most HCV+ patients with HCC benefit from DAA treatment; however, timing of DAA initiation after HCC treatment should be carefully considered.
随着直接作用抗病毒药物(DAA)的出现,丙型肝炎病毒(HCV)的治疗效果显著提高。尽管少数研究报告了 DAA 治疗后肝细胞癌(HCC)复发的发生率,但尚无研究对成功治疗 HCC 后接受足够数量 DAA 治疗的患者进行 HCC 复发的随访。
我们进行了一项队列研究,纳入了在开始使用 DAA 之前成功治疗 HCC 的 HCV+患者。我们进行了病历回顾,以确认 DAA 开始前 HCC 的诊断、治疗和缓解情况,以及随后的 HCC 复发情况。我们计算了 HCC 复发率,并检查了复发性肿瘤的特征。我们使用 Cox 比例风险模型来确定与 HCC 复发相关的因素。
我们共纳入了 264 例 HCV+患者,这些患者在 HCC 治疗后平均 30.9(20.6)个月接受了 DAA 治疗。在 23.3(9.8)个月的随访期间,26.1%的患者发生 HCC 复发,复发率为 0.38[0.30,0.48]每 1000 人月。大多数(82.3%)复发 HCC 处于早期阶段。与根治性治疗相比,非根治性 HCC 治疗与更高的 HCC 复发风险相关(HR=2.06[1.24,3.40])。HCC 治疗完成与 DAA 开始之间的时间间隔越长,HCC 复发的风险越低(HR=0.97[0.95,0.99]每额外一个月)。与获得持续病毒学应答(SVR)的患者相比,未获得 SVR 的患者 HCC 复发的风险显著增加(HR=4.17[1.48,11.75])。
我们的结论是,大多数患有 HCC 的 HCV+患者从 DAA 治疗中受益;然而,DAA 治疗后开始治疗的时间应仔细考虑。