Department of Basic Medical Sciences, The School of Health Sciences in Bytom, Medical University of Silesia, Bytom 41-902, Poland.
Department of Animal Physiology, Faculty of Biology, University of Warsaw, Warszawa 02-096, Poland.
World J Gastroenterol. 2021 May 14;27(18):2177-2192. doi: 10.3748/wjg.v27.i18.2177.
The introduction of direct-acting antiviral drugs into clinical practice has revolutionized the treatment of chronic hepatitis C, making it highly effective and safe for patients. However, few researchers have analyzed the factors causing therapy failure in some patients.
To analyze factors influencing the failure of direct antiviral drugs in the large, multicenter EpiTer-2 cohort in a real-world setting.
The study cohort consisted of patients with chronic hepatitis C treated at 22 Polish centers from 2016-2020. Data collected from the online EpiTer-2 database included the following: hepatitis C virus (HCV) genotype, stage of fibrosis, hematology and liver function parameters, Child-Turcotte-Pugh and Model for End-stage Liver Disease scores, prior antiviral therapy, concomitant diseases, and drugs used in relation to hepatitis B virus (HBV) and/or human immunodeficiency virus (HIV) coinfections. Adverse events observed during the treatment and follow-up period were reported. Both standard and machine learning methods were used for statistical analysis.
During analysis, 12614 patients with chronic hepatitis C were registered, of which 11938 (mean age: 52 years) had available sustained virologic response (SVR) data [11629 (97%) achieved SVR and 309 (3%) did not]. Most patients (78.1%) were infected with HCV genotype 1b. Liver cirrhosis was diagnosed in 2974 patients, while advanced fibrosis (F3) was diagnosed in 1717 patients. We included patients with features of hepatic failure at baseline [ascites in 142 (1.2%) and encephalopathy in 68 (0.6%) patients]. The most important host factors negatively influencing treatment efficacy were liver cirrhosis, clinical and laboratory features of liver failure, history of hepatocellular carcinoma, and higher body mass index. Among viral factors, genotype 3 and viral load also exerted an influence on treatment efficacy. Classical statistical analysis revealed that treatment ineffectiveness seemed to be influenced by the male sex, which was not confirmed by the multivariate analysis using the machine learning algorithm (random forest). Coinfection with HBV (including patients with on-treatment reactivation of HBV infection) or HIV, extrahepatic manifestations, and renal failure did not significantly affect the treatment efficacy.
In patients with advanced liver disease, individualized therapy (testing for resistance-associated variants and response-guided treatment) should be considered to maximize the chance of achieving SVR.
直接作用抗病毒药物在临床实践中的引入彻底改变了慢性丙型肝炎的治疗方法,使该治疗对患者既高效又安全。然而,很少有研究人员分析导致某些患者治疗失败的因素。
分析在真实环境中,大型多中心 EpiTer-2 队列中直接抗病毒药物治疗失败的影响因素。
研究队列由 2016 年至 2020 年期间在波兰 22 个中心接受治疗的慢性丙型肝炎患者组成。从在线 EpiTer-2 数据库中收集的数据包括:丙型肝炎病毒(HCV)基因型、纤维化分期、血液学和肝功能参数、Child-Turcotte-Pugh 和终末期肝病模型评分、既往抗病毒治疗、合并症以及与乙型肝炎病毒(HBV)和/或人类免疫缺陷病毒(HIV)合并感染相关的药物。报告了治疗和随访期间观察到的不良事件。使用标准和机器学习方法进行统计分析。
在分析过程中,共登记了 12614 例慢性丙型肝炎患者,其中 11938 例(平均年龄 52 岁)有持续病毒学应答(SVR)数据[11629 例(97%)获得 SVR,309 例(3%)未获得]。大多数患者(78.1%)感染 HCV 基因型 1b。2974 例患者诊断为肝硬化,1717 例患者诊断为晚期纤维化(F3)。我们纳入了基线时具有肝功能衰竭特征的患者[腹水 142 例(1.2%),脑病 68 例(0.6%)]。对治疗效果有重要负面影响的宿主因素主要为肝硬化、肝衰竭的临床和实验室特征、肝细胞癌病史和较高的体重指数。在病毒因素中,基因型 3 和病毒载量也对治疗效果有影响。经典统计学分析表明,治疗无效似乎受男性性别影响,但使用机器学习算法(随机森林)进行多变量分析并未证实这一点。HBV 合并感染(包括治疗期间 HBV 感染再激活的患者)或 HIV 合并感染、肝外表现和肾衰竭并不显著影响治疗效果。
在患有晚期肝病的患者中,应考虑个体化治疗(检测耐药相关变异和基于应答的治疗),以最大程度提高获得 SVR 的机会。