Zhou H, Luo H, Xiao S, Wang H, Gong G
Department of Infectious Diseases, the Second Xiangya Hospital, Central South University, 139 Renming Middle Road, Changsha, Hunan Province, 410011, China.
Eur J Clin Microbiol Infect Dis. 2014 Apr;33(4):491-8. doi: 10.1007/s10096-013-1992-8. Epub 2013 Nov 6.
Treatment-related adverse events (AE) were more frequent in older patients treated by pegylated interferon (PEG-IFN) plus ribavirin (RBV) for chronic hepatitis C (CHC), and most of them required dose reduction. A meta-regression analysis was conducted to explore the possible reasons for this occurrence. We searched MEDLINE, EMBASE, and Web of Science through May 2013, for clinical trials examining the safety of PEG-IFN plus RBV in elderly patients with CHC. Data were extracted for host, viral, and outcome information. Single-arm meta-analysis was performed to evaluate AE. Meta-regression analysis was conducted to explore predictors for dose reduction secondary to AE. Eighteen observational studies met the inclusion criteria. The overall incidences of AE were 61.3%. Dose reductions due to AE were 54.2%. In patients with genotype 1, the rate of sustained virological response (SVR) was 36.9%. In patients with genotypes 2 or 3, the rate of SVR was 72.8%. Patients with more dose reduction due to AE have a tendency toward a lower likelihood of obtaining SVR (coefficient:-0.529), especially for genotype 1 patients. Host factors (male gender, coefficient 4.403; higher body weight, coefficient 0.140; and advanced fibrosis stage, coefficient 1.582) and viral factors (HCV genotype 1, coefficient 2.279) have a significant impact on dose reduction due to AE. Some host and viral factors affected dose reduction due to AE. Increasing rates of fibrosis with age may play a role as a mechanism affecting dose reduction secondary to AE and SVR in different age groups.
聚乙二醇干扰素(PEG - IFN)联合利巴韦林(RBV)治疗慢性丙型肝炎(CHC)时,老年患者的治疗相关不良事件(AE)更为频繁,且大多数不良事件需要减少剂量。进行了一项Meta回归分析以探究出现这种情况的可能原因。我们检索了截至2013年5月的MEDLINE、EMBASE和科学网,查找关于PEG - IFN联合RBV治疗老年CHC患者安全性的临床试验。提取了宿主、病毒和结局信息的数据。进行单臂Meta分析以评估不良事件。进行Meta回归分析以探究因不良事件导致剂量减少的预测因素。18项观察性研究符合纳入标准。不良事件的总体发生率为61.3%。因不良事件导致的剂量减少率为54.2%。基因1型患者的持续病毒学应答(SVR)率为36.9%。基因2或3型患者的SVR率为72.8%。因不良事件导致更多剂量减少的患者获得SVR的可能性有降低趋势(系数:-0.529),尤其是基因1型患者。宿主因素(男性,系数4.403;体重较高,系数0.140;纤维化晚期,系数1.582)和病毒因素(HCV基因1型,系数2.279)对因不良事件导致的剂量减少有显著影响。一些宿主和病毒因素影响了因不良事件导致的剂量减少。随着年龄增长纤维化发生率增加可能是影响不同年龄组因不良事件导致剂量减少及SVR的一种机制。