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Bendamustine‐associated infections—systematic review and meta‐analysis of randomized controlled trials

机译:弯曲蛋白质相关的感染 - 系统评价和随机对照试验的荟萃分析

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Abstract Data in the literature are lacking regarding the infection‐related adverse events of bendamustine‐containing regimens. Therefore, we aimed to assess this risk. We conducted a systematic review and meta‐analysis of all randomized controlled trials including bendamustine‐containing regimens and those administered for any lymphoproliferative disorder or plasma cell dyscrasia compared with any other regimens. A comprehensive search was conducted until December 2015. Two reviewers appraised the quality of trials and extracted data. Primary outcomes were any infections, grade 3 to 4 infections; secondary outcomes were grade 3 to 4 neutropenia and grade 3 to 4 lymphopenia. Relative risks (RRs) with 95% confidence intervals (CIs) were estimated and pooled. A fixed‐effect model was used to pool data unless there was significant heterogeneity, in which case a random‐effects model was used. Nine trials published between 2006 and 2016 and randomizing 2620 patients were included. There was no statistically significant effect for bendamustine on the rate of any infection (RR 1.09 [95% CI, 0.87‐1.36]) or on the rate of grade 3 to 4 infections (RR 1.04 [95% CI, 0.64‐1.71]). There was no increase in the rate of grade 3 to 4 neutropenia in the bendamustine arm (RR 0.84 [95% CI, 0.63‐1.12]). Our systematic review demonstrates no effect of bendamustine on the rate of infections when compared with either alkylating agents or fludarabine. Thus, bendamustine remains a safe therapeutic option.
机译:文献中缺乏关于含苯达莫司汀方案的感染相关不良事件的抽象数据。因此,我们旨在评估这种风险。我们对所有随机对照试验进行了系统回顾和荟萃分析,包括含苯达莫司汀的方案,以及与任何其他方案相比针对任何淋巴增生性疾病或浆细胞紊乱的方案。在2015年12月之前进行了全面搜索。两位评审员评估了试验的质量并提取了数据。主要转归是任何感染,3至4级感染;次要转归为3-4级中性粒细胞减少和3-4级淋巴细胞减少。估计并汇总95%置信区间(CI)的相对风险(RRs)。除非存在显著的异质性,否则使用固定效应模型来汇集数据,在这种情况下,使用随机效应模型。包括2006年至2016年间发表的9项试验,并随机抽取2620名患者。苯达莫司汀对任何感染率(RR 1.09[95%CI,0.87-1.36])或3-4级感染率(RR 1.04[95%CI,0.64-1.71])均无统计学显著影响。苯达莫司汀组的3-4级中性粒细胞减少率没有增加(RR 0.84[95%可信区间,0.63-1.12])。我们的系统评价表明,与烷化剂或氟达拉滨相比,苯达莫司汀对感染率没有影响。因此,本达莫司汀仍是一种安全的治疗选择。

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