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首页> 外文期刊>Medicine. >Direct acting antivirals treatment for hepatitis C virus infection does not increase the incidence of de novo hepatocellular carcinoma occurrence: Results from an Italian real-life cohort (LINA cohort)
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Direct acting antivirals treatment for hepatitis C virus infection does not increase the incidence of de novo hepatocellular carcinoma occurrence: Results from an Italian real-life cohort (LINA cohort)

机译:直接代理抗病毒药物治疗丙型肝炎病毒感染不会增加Novo肝细胞癌发生的发病率:意大利现实队列(Lina Cohort)的结果

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摘要

The effectiveness of direct-acting antivirals (DAAs) against hepatitis C virus ( HCV ) infection is ascertained. However, some authors raised the issue of an increased incidence of de novo hepatocellular carcinoma (HCC) in patients treated with DAAs. Aim of the study was to evaluate the rate of HCC occurrence in a real-life cohort of patients who received anti- HCV treatment with DAAs. A prospective multicentre study was conducted. All adult patients with HCV infection who received treatment between March 2015 and December 2017 in 4 hospital of Campania region (South Italy) with at least 6 months of follow-up were enrolled. A total of 323 patients were included in the study. Most patients had HCV genotype 1b (61.8%). The overall SVR12 rate was 95.5%. Median time of observation was 10 months. The incidence rate of HCC was 0.2 per 100 person-months (crude incidence rate 3.4%, 95 confidence interval: 1.5%–5.3%). The median time for HCC occurrence was 11 months. HCC occurrence rate was significantly higher among patients who did not achieve SVR12 compared with patients who did (28.6% vs 2.8%, P 0.05). No patient with F0-F3 fibrosis developed HCC. Among patients with cirrhosis, at the multivariate time-to-event analysis, no covariates were independently associated with the risk of HCC occurrence. Treatment with DAAs did not increase the risk of HCC occurrence. Patients who achieved SVR12 had a lower rate of HCC occurrence. Further studies are needed to estimate the incidence and the risk for HCC in the long-term follow-up among patients undergoing treatment with DAAs.
机译:确定直接作用抗病毒(DAAS)对丙型肝炎病毒(HCV)感染的有效性。然而,一些作者提出了DAA治疗的患者De Novo肝细胞癌(HCC)发病率增加的问题。该研究的目的是评估HCC发生的率在接受DAAS抗HCV治疗的患者的现实生活队列中。进行了一项预期的多月份研究。所有有HCV感染的成年患者于2015年3月和2017年12月在坎帕尼亚地区(南意大利)40次接受待遇,至少有6个月的随访。该研究中共有323名患者。大多数患者有HCV基因型1B(61.8%)。整体SVR12率为95.5%。观察时间是10个月。 HCC的发病率为每100人的0.2个月(粗产率3.4%,95次置信区间:1.5%-5.3%)。 HCC发生的中位时间为11个月。与患者未达到SVR12的患者(28.6%Vs 2.8%,P <0.05)相比,HCC发生率显着高。没有患有F0-F3纤维化的患者发育了HCC。在肝硬化患者中,在多变量的时间 - 事件分析中,没有协调因子与HCC发生的风险独立相关。 DAA治疗没有增加HCC发生的风险。达到SVR12的患者率较低的HCC发生率。需要进一步的研究来估算与DAAS治疗患者的长期随访中HCC的发病率和风险。

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