Internal Medicine and Hepatology Unit, University of Salerno, Salerno, Italy.
Liver Int. 2019 Jul;39(7):1292-1306. doi: 10.1111/liv.14119. Epub 2019 May 8.
Direct antiviral agents have greatly improved therapeutic options for chronic hepatitis C. Indeed, former "difficult-to-treat" patients can now be treated and can achieve sustained response. Hepatitis C virus (HCV) is associated with hepatocellular carcinoma and with B-cell non-Hodgkin lymphoma (B-NHL). Other malignancies have been reported to be associated with HCV infection albeit with various grades of evidence. Antineoplastic treatment is often reduced or suspended in HCV-positive cancer patients to avoid "HCV reactivation." In this setting, antiviral therapy combined with antineoplastic protocols may improve the outcome. For this reason, we conducted a systematic review and a meta-analysis to update the association between HCV infection and non-hepatocellular malignancies, and to shed light on the effects exerted by antiviral treatment on the natural history of oncological diseases.
Relevant studies were identified by searching PUBMED, EMBASE and MEDLINE up to 1 August 2018. Pooled risk estimates were calculated with random-effects models according to PRISMA guidelines.
A total of 58 studies were included in the analysis: 27 studies of the association between HCV and B-NHL(OR 3.36; 95% CI 2.40-4.72;P < 0.00001);13 studies of the association between sustained virological response and progression-free survival (PFS) in B-NHL patients(OR 9.34; 95% CI 4.90-17.79; P < 0.00001); 13 studies of the association between HCV and intrahepatic-cholangio-carcinoma (OR 3.95;95% CI 2.25-6.94; P < 0.00001); and 5 studies of the association between HCV infection and pancreatic adeno-carcinoma(OR 1.60; 95% CI:1.25-2.04; P = 0.0002).
This study updates the strong association between B-NHL and HCV infection, confirms the association between HCV and non-hepatocellular tumours, and demonstrates a very strong association between viral eradication and a better outcome of HCV-positive B-NHL.
直接抗病毒药物极大地改善了慢性丙型肝炎的治疗选择。事实上,以前的“难治”患者现在可以接受治疗并获得持续应答。丙型肝炎病毒(HCV)与肝细胞癌和 B 细胞非霍奇金淋巴瘤(B-NHL)相关。尽管证据程度不同,但其他恶性肿瘤也与 HCV 感染相关。为避免“HCV 再激活”,HCV 阳性癌症患者的抗肿瘤治疗常被减少或暂停。在这种情况下,抗病毒治疗联合抗肿瘤方案可能会改善预后。出于这个原因,我们进行了系统评价和荟萃分析,以更新 HCV 感染与非肝细胞恶性肿瘤之间的关联,并阐明抗病毒治疗对肿瘤疾病自然史的影响。
通过搜索 PUBMED、EMBASE 和 MEDLINE,我们在 2018 年 8 月 1 日之前确定了相关研究。根据 PRISMA 指南,使用随机效应模型计算汇总风险估计值。
共有 58 项研究纳入分析:27 项研究评估了 HCV 与 B-NHL 之间的关联(OR 3.36;95%CI 2.40-4.72;P<0.00001);13 项研究评估了持续病毒学应答与 B-NHL 患者无进展生存期(PFS)之间的关联(OR 9.34;95%CI 4.90-17.79;P<0.00001);13 项研究评估了 HCV 与肝内胆管癌(OR 3.95;95%CI 2.25-6.94;P<0.00001)之间的关联;5 项研究评估了 HCV 感染与胰腺腺癌之间的关联(OR 1.60;95%CI:1.25-2.04;P=0.0002)。
本研究更新了 B-NHL 与 HCV 感染之间的强关联,证实了 HCV 与非肝细胞肿瘤之间的关联,并表明病毒清除与 HCV 阳性 B-NHL 更好的预后之间存在很强的关联。