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首页> 外文期刊>Journal of viral hepatitis. >Direct‐acting antivirals reduce the risk of tumour progression of hepatocellular carcinoma after curative treatment
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Direct‐acting antivirals reduce the risk of tumour progression of hepatocellular carcinoma after curative treatment

机译:直接作用抗病毒药物可降低根治性治疗后肝细胞癌肿瘤进展的风险

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Abstract Hepatocellular carcinoma (HCC) has high recurrence rates. HCC sometimes progresses from early‐stage HCC (Barcelona Clinic Liver Cancer BCLC stage 0/A) to advanced‐stage HCC after repeated recurrences and treatments. HCC progression deteriorates quality of life and prognosis. However, the effect of direct‐acting antiviral (DAA)‐induced sustained virologic response (SVR) on HCC progression remains uninvestigated. We conducted a retrospective cohort study of patients with hepatitis C virus‐related HCC with BCLC stage 0/A diagnosed for the first time and treated by curative resection or ablation. Using a time‐varying method, we estimated the risk of tumour progression (defined as progression to BCLC stage B‐D) and liver‐related death and the characteristics of repeated recurrence. Overall, 165 patients were enrolled. Following curative HCC treatment, 72 patients received DAA therapy (DAA‐treated group), whereas 93 did not (untreated group). Approximately 75 of the recurrences were at an early stage and expected to be disease‐free by retreatment. We recorded 56 tumour progressions, of which 60.7 were observed after second recurrence. Multivariate adjusted time‐varying Cox regression analysis showed that the DAA‐induced SVR significantly reduced the risk of tumour progression (hazard ratio HR 0.28; p?=?.001) and liver‐related death (HR 0.12; p?
机译:摘要 肝细胞癌(HCC)的复发率较高。HCC 有时会在反复复发和治疗后从早期 HCC(巴塞罗那诊所肝癌 [BCLC] 0/A 期)进展为晚期 HCC。肝细胞癌进展会恶化生活质量和预后。然而,直接作用抗病毒 (DAA) 诱导的持续病毒学反应 (SVR) 对 HCC 进展的影响仍未得到研究。我们对首次诊断为BCLC 0/A期的丙型肝炎病毒相关HCC患者进行了一项回顾性队列研究,并接受了根治性切除或消融治疗。使用时变方法,我们估计了肿瘤进展(定义为进展到 BCLC B-D 期)和肝脏相关死亡的风险以及反复复发的特征。总共招募了 165 名患者。在根治性HCC治疗后,72例患者接受了DAA治疗(DAA治疗组),而93例患者未接受DAA治疗(未治疗组)。大约75%的复发处于早期阶段,预计通过再治疗将无病。我们记录了 56 例肿瘤进展,其中 60.7% 是在第二次复发后观察到的。多因素校正时变Cox回归分析显示,DAA诱导的SVR显著降低了肿瘤进展的风险(HR 0.28;p?=?。001)和肝脏相关死亡(HR 0.12;001).HCC治疗直至肿瘤进展的年发生率为82.8%和23.未治疗组和DAA治疗组分别为9%(HR 0.30;001). DAA 诱导的 SVR 显著降低了 BCLC 0/A 期 HCC 根治性治疗后肿瘤进展和肝脏相关死亡的风险以及 HCC 治疗的频率。

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