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首页> 外文期刊>Clinical lymphoma, myeloma & leukemia >Randomized Controlled Trials in Relapsed/Refractory Chronic Lymphocytic Leukemia: A Systematic Review and Meta-Analysis
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Randomized Controlled Trials in Relapsed/Refractory Chronic Lymphocytic Leukemia: A Systematic Review and Meta-Analysis

机译:复发/难治性慢性淋巴细胞白血病的随机对照试验:系统评价和荟萃分析

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摘要

This systematic literature review with meta-analysis was conducted on the clinical efficacy and safety of interventions used in the treatment of chronic lymphocytic leukemia (CLL). We systematically searched databases (PubMed, Cochrane Library, and Embase; 1997 to August 2, 2012), conference abstracts, bibliographic reference lists, recent reviews, and Clinicaltrials.gov. Primary efficacy outcomes were objective response rate, progression-free survival, and overall survival. Safety end points were Grade 3/4 toxicities, serious adverse events, withdrawals because of toxicity, and deaths due to toxicity. Studies were selected if they were randomized controlled trials (RCTs) reporting on the efficacy or safety of relapsed or refractory CLL and if outcomes for CLL were reported separately from trials that included other lymphoid neoplasms. We used the Bucher method for conducting adjusted indirect comparisons within a meta-analysis. We identified 6 RCTs of pharmacologic treatment for relapsed/refractory CLL. The most common drugs investigated (alone or in combination) were fludarabine and cyclophosphamide. When reported, median overall survival ranged from 27.3 to 52.9 months, and overall response rate from 58% to 82%. Although meta-analysis of efficacy results was considered, details are not presented because only 3 studies qualified and the common comparator treatment was not clinically relevant. The relatively small number of RCTs, few overlapping treatment arms, and variability in end points studied make it difficult to formally compare therapies for relapsed/refractory CLL. Significant variability in RCT features presents a further challenge to meaningful comparisons. Additional well-designed RCTs are needed to fully understand the relative efficacy and safety of older and more recently developed therapies. (C) 2015 Elsevier Inc. All rights reserved.
机译:这项荟萃分析的系统性文献综述针对用于治疗慢性淋巴细胞性白血病(CLL)的干预措施的临床疗效和安全性进行了研究。我们系统地搜索了数据库(PubMed,Cochrane图书馆和Embase; 1997年至2012年8月2日),会议摘要,书目参考书目,近期评论和Clinicaltrials.gov。主要疗效结果是客观缓解率,无进展生存期和总体生存期。安全终点为3/4级毒性,严重的不良事件,因毒性而停药以及因毒性而死亡。如果研究是复发或难治性CLL的疗效或安全性的随机对照试验(RCT),并且与其他淋巴样肿瘤的试验分开报告了CLL的结果,则选择这些研究。我们使用Bucher方法在荟萃分析中进行了调整后的间接比较。我们确定了针对复发/难治性CLL的6种药物治疗的RCT。研究的最常见药物(单独或联合使用)是氟达拉滨和环磷酰胺。报告时,中位总生存期为27.3至52.9个月,总缓解率从58%至82%。尽管考虑了疗效结果的荟萃分析,但由于只有3项研究合格且普通的比较药物治疗与临床无关,因此未提供详细信息。相对较少的RCT,很少的重叠治疗臂以及研究终点的可变性使得很难正式比较复发/难治性CLL的疗法。 RCT功能的显着可变性对有意义的比较提出了进一步的挑战。还需要其他设计良好的RCT,以充分了解较旧和最近开发的疗法的相对疗效和安全性。 (C)2015 Elsevier Inc.保留所有权利。

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