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首页> 外文期刊>Hepatology: Official Journal of the American Association for the Study of Liver Diseases >The short‐term incidence of hepatocellular carcinoma is not increased after hepatitis C treatment with direct‐acting antivirals: An ERCHIVES study
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The short‐term incidence of hepatocellular carcinoma is not increased after hepatitis C treatment with direct‐acting antivirals: An ERCHIVES study

机译:用直接作用抗病毒杀虫治疗丙型肝炎治疗后,肝细胞癌短期发病率不会增加:溶液研究

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Recent studies have reported higher rates of hepatocellular carcinoma (HCC) in individuals treated with direct‐acting antivirals (DAAs). However, making definitive conclusions has been challenging because of the heterogeneous populations and methodologies of these reports. We investigated whether DAA use is associated with higher rates of incident HCC compared to treatment with interferon (IFN)‐based regimens. We performed a retrospective, population‐based cohort study using the Electronically Retrieved Cohort of HCV Infected Veterans (ERCHIVES) database. In a cohort of 17,836 persons, sustained virological response (SVR) was achieved by 66.6% and 96.2% of the IFN and DAA groups, respectively. Among all treated persons, risk of HCC was not higher in the DAA group compared to the IFN group (hazard ratio, 1.07; 95% confidence interval, 0.55, 2.08). Among persons with cirrhosis who achieved SVR, neither the HCC incidence rate nor HCC‐free survival were significantly different in the DAA group compared to the IFN group (21.2 vs. 22.8 per 1,000 person‐years; P = 0.78 and log‐rank P = 0.17, respectively). Untreated persons with cirrhosis had a significantly higher HCC incidence rate (45.3 per 1,000 person‐years) compared to those treated with either IFN or DAAs ( P = 0.03). Both groups of treated persons had significantly lower probability of HCC development compared to untreated persons (log‐rank, P = 0.0004). Conclusion: DAA treatment is not associated with a higher risk of HCC in persons with cirrhosis with chronic HCV infection in the short term. Previously reported higher rates of HCC associated with DAA treatment may be explained by both the presence of relatively fewer baseline HCC risk factors in persons treated with IFN as well as selection bias, given that DAA regimens were used to treat persons at higher risk for developing HCC. (H epatology 2018;67:2244‐2253).
机译:最近的研究报告了用直接作用抗病毒药物(DAAS)治疗的个体中肝细胞癌(HCC)的较高速率。然而,由于这些报告的异质人口和方法,使确定的结论是挑战性的。我们调查了与干扰素(IFN)的治疗相比,DAA使用是否与较高的事故HCC速率相关联。我们使用电子检索的HCV感染的退伍军人(erchives)数据库进行了追溯,基于人口的群组研究。在17,836人的队列中,持续的病毒学反应(SVR)分别取得了66.6%和96.2%的IFN和DAA组。在所有处理的人中,与IFN组(危险比为1.07; 95%置信区间,0.55,2.08),DAA组HCC风险不高。在患有SVR的肝硬化的人中,与IFN组相比,DAA组中HCC发病率和HCC的存活率都没有显着不同(21.2与每1000人 - 年份; P = 0.78和log-Rank P = 0.17分别)。与用IFN或DAAS处理的人相比,未经治疗的肝硬化的人具有显着较高的HCC发病率(每1000人 - 年45.3)(P = 0.03)。与未经处理的人员相比,两组治疗的人和HCC开发概率明显降低了(对数秩,P = 0.0004)。结论:DAA治疗与短期内肝硬化的肝硬化的人患有更高的HCC风险无关。先前,鉴于DAA方案用于治疗发展HCC的风险较高的人,可以通过对DAA治疗的存在相对较少的基线HCC风险因素的存在较高的与DAA治疗相关的HCC率的较高率。 。 (2018年,2018; 67:2244-2253)。

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