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首页> 外文期刊>Alimentary pharmacology & therapeutics. >Direct‐acting antiviral treatment for hepatitis C virus infection and risk of incident liver cancer: a retrospective cohort study
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Direct‐acting antiviral treatment for hepatitis C virus infection and risk of incident liver cancer: a retrospective cohort study

机译:用于丙型肝炎病毒感染的直接作用抗病毒治疗和事故肝癌的风险:回顾性队列研究

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Summary Background Eradication of hepatitis C virus ( HCV ) infection via interferon‐based treatment lowers hepatocellular carcinoma risk; some research suggests this effect extends to interferon‐free treatment. Aims The objective of this retrospective cohort study was to examine the association of direct‐acting antiviral ( DAA ) exposure with risk of incident liver cancer in real‐world data. Methods From United States administrative claims data through March 31, 2017, we identified 30 183 adult HCV patients exposed to DAA s. For comparison, we identified contemporary adult HCV patients without evidence of HCV treatment (N = 137 502), and historical HCV patients treated with interferon prior to the introduction of DAA s (N = 12 948). Included patients had at least 12 months of prior enrolment and no evidence of prior liver cancer at baseline. Hazard ratios ( HR s) estimating risk of incident liver cancer associated with DAA treatment were calculated using Cox proportional hazards methods. Results Relative to untreated HCV patients, DAA ‐treated patients were older, more likely to be male, and more likely to have cirrhosis at baseline. After adjustment, DAA treatment was associated with a significantly reduced risk of liver cancer relative to no treatment (adjusted HR = 0.84, 95% CI : 0.73‐0.96), and relative to interferon‐based treatment in the pre‐ DAA era ( HR = 0.69, 95% CI : 0.59‐0.81). Conclusions In this large, population‐based study, DAA ‐based treatment was associated with a reduced risk of incident liver cancer relative to both no HCV treatment and to interferon‐based treatment in the pre‐ DAA era. As additional follow‐up time of DAA ‐treated patients accrues, we anticipate that the long‐term benefits of DAA treatment will become more apparent.
机译:发明内容背景消除丙型肝炎病毒(HCV)感染通过干扰素的治疗降低肝细胞癌风险;一些研究表明这种效果延伸到无干扰素治疗。目的是,这项回顾性队列队列研究的目的是检查直接作用抗病毒(DAA)暴露在现实世界数据中发生肝癌风险的关联。方法从美国行政索赔数据到2017年3月31日,我们确定了30名183名183名暴露于DAA S的成人HCV患者。为了比较,我们鉴定了当代成年HCV患者,没有HCV治疗的证据(n = 137 502),以及在引入DAA S(n = 12 948)之前用干扰素治疗的历史HCV患者。包括患者的患者至少有12个月的招生,并且在基线上没有证据表明肝癌。利用COX比例危害方法计算危险比(HRS)估算与DAA治疗相关的入射肝癌风险。结果相对于未经治疗的HCV患者,DAA -Treated患者年龄较大,更可能是男性,并且更有可能在基线上具有肝硬化。调整后,DAA治疗与相对于无处理的肝癌风险显着降低(调节的HR = 0.84,95%CI:0.73-0.96),以及在DAA时代的干扰素的治疗(HR = 0.69,95%CI:0.59-0.81)。结论在这一大,基于人群的研究中,DAA基础的治疗与事件肝癌的风险降低有关,相对于NO HCV治疗和在DAA时代的干扰素的治疗中有关。作为DAA-治疗患者的额外后续时间,我们预计DAA治疗的长期益处将变得更加明显。

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