丙型肝炎治愈后,肝硬化患者仍有患肝细胞癌风险的障碍。

Hepatology, medicine and policy Pub Date : 2016-09-23 eCollection Date: 2016-01-01 DOI:10.1186/s41124-016-0019-3
Soo Aleman
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引用次数: 0

摘要

新的直接作用抗病毒药物(DAAs)问世后,丙型肝炎的治愈率大幅提高,尤其是肝硬化患者。在以往基于干扰素(IFN)治疗的研究中,肝硬化患者治愈后罹患肝细胞癌(HCC)的风险有所降低,但仍然存在。随着接受治疗和治愈的肝硬化患者人数急剧增加,HCC 风险有望成为丙型肝炎患者管理中的下一个障碍。在最近于西班牙巴塞罗那举行的 2016 年国际肝脏大会上,Buonfiglioli F 等人针对接受 DAAs 治疗的既往 HCC 患者提交了一份可能令人担忧的报告。这份初步报告显示,接受过 DAA 治疗的 HCC 患者在开始接受 DAA 治疗后,在治疗后 12-24 周的随访中,HCC 早期复发率高达 29%。就在这份报告之前,Reig M 等人发表的另一项研究也显示了类似的 HCC 高复发率。在这项研究中,研究人员对接受过消融、切除或经动脉化疗栓塞治疗的 HCC 患者进行了分析,以了解他们在接受 DAA 治疗后 HCC 复发的风险。中位随访时间为 5.7 个月,HCC 复发率为 28%。这些研究的缺点是缺乏对照组,但与之前的研究相比,这些数字出乎意料地高。这些研究结果需要进一步探讨,并最终在其他研究中得到证实,然后才能得出明确结论并改变常规做法。在我们获得更多数据之前,必须根据个体情况,权衡这些 DAAs 的早期 HCC 复发风险和其他风险,以及阻止肝病进展的其他益处。
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The hurdle with remaining risk for hepatocellular carcinoma in cirrhotic patients after a hepatitis C cure.

After introduction of new direct acting antivirals (DAAs) against hepatitis C, the cure rate has increased substantially especially in patients with liver cirrhosis. Decreased but remaining risk for hepatocellular carcinoma (HCC) has been shown in patients with liver cirrhosis after cure, in previous studies with interferon (IFN)-based treatments. This risk for HCCs is expected to become the next hurdle in the management of hepatitis C patients, as the number of treated and cured patients with liver cirrhosis is increasing dramatically. At the recent International Liver Congress 2016, Barcelona, Spain, a potentially alarming report was presented by Buonfiglioli F et al., among otherwise positive reports, for patients with prior HCC being treated with DAAs. This preliminary report showed a high early recurrence rate of 29 % for HCC after initiation of DAA treatment in patients with treated HCC, at follow-ups 12-24 weeks post-treatment. Another study was published just prior to this report by Reig M et al. showing similarly high recurrence rate for HCC. In this study, patients who have been treated for HCC with ablation, resection or transarterial chemoembolization, and no sign of remaining HCC at treatment start, were analysed for the risk of HCC recurrence after DAA treatment initiation. After a median follow-up time of 5.7 months, recurrence rate of HCC was seen in 28 %. The disadvantage of these studies was the lack of any control group, but these figures were unexpectedly high compared to figures in previous studies. These findings need to be further explored and eventually confirmed in other studies before making any firm conclusions and change of the routine practice. Until we have more data, the eventual risks for early HCC recurrence and other risks must be weighed against other benefits of these DAAs, halting liver disease progression, on an individual basis.

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Correlates of hepatitis B awareness and disease-specific knowledge among pregnant women in Northern and Central Uganda: a cross-sectional study. Correction to: Hepatology, Medicine and Policy: Articles with DOIs 10.1186/s41124-016-0014-8, 10.1186/s41124-016-0013-9 and 10.1186/s41124-016-0012-x. Strategies for achieving viral hepatitis C micro-elimination in the Netherlands. Erratum: Publisher Correction to Hepatology, Medicine and Policy: Articles with DOIs 10.1186/s41124-017-0024-1, 10.1186/s41124-017-0025-0, 10.1186/s41124-017-0026-z and 10.1186/s41124-017-0027-y. Seroprevalence of hepatitis B and C in Nepal: a systematic review (1973-2017).
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