...
首页> 外文期刊>Haematologica >Systematic review of purine analog treatment for chronic lymphocytic leukemia: Lessons for future trials
【24h】

Systematic review of purine analog treatment for chronic lymphocytic leukemia: Lessons for future trials

机译:嘌呤类似物治疗慢性淋巴细胞白血病的系统评价:未来试验的经验教训

获取原文
获取原文并翻译 | 示例
           

摘要

A systematic review of purine analogs revealed heterogeneity between trials in treatment effects on response and progression free survival, but not survival, perhaps partly due to variations in analytical methods. In addition, combination treatments required evaluation. Therefore, individual patient data were sought for all randomized trials in untreated chronic lymphocytic leukemia which involved a purine analog, but which did not include antibody therapies. Sixteen trials were found, addressing seven comparisons. Eight trials, with 2,753 patients, showed that single agent purine analog improved progression free survival (odds ratio=0.71; 95 confidence interval=0.63- 0.79). Heterogeneity remained substantial. Three trials, with 1,403 patients, showed that progression free survival was further improved by the addition of cyclophosphamide (odds ratio=0.54; 0.47-0.62). Fewer data were available on the addition of other drugs to purine analog, and none showed clear benefit. Two trials, with 544 patients, suggested cladribine improved progression free survival compared to fludarabine (odds ratio=0.77; 0.63-0.95). No differences were seen in overall survival for any comparisons. In conclusion, purine analogs, particularly combined with cyclophosphamide, significantly improve progression free survival but not survival. Some groups, such as the elderly, may not see the same benefits and maximizing doses may be important for all treatments, including chlorambucil. Longer follow up, consistent definitions and detailed reporting of trials should be encouraged.
机译:一项关于嘌呤类似物的系统评价显示,在治疗对反应和无进展生存期的影响方面,试验之间存在异质性,但对生存率没有影响,部分原因可能是分析方法的差异。此外,联合治疗需要评估。因此,所有涉及嘌呤类似物但不包括抗体疗法的未经治疗的慢性淋巴细胞白血病的随机试验都寻求个体患者数据。共纳入16项试验,涉及7项比较。涉及2,753名患者的8项试验显示,单药嘌呤类似物可改善无进展生存期(比值比=0.71;95%置信区间=0.63-0.79)。异质性仍然很大。三项涉及1,403名患者的试验显示,添加环磷酰胺可进一步改善无进展生存期(比值比=0.54;0.47-0.62)。关于在嘌呤类似物中添加其他药物的数据较少,也没有显示出明显的益处。两项涉及544名患者的试验表明,与氟达拉滨相比,克拉屈滨可改善无进展生存期(比值比=0.77;0.63-0.95)。对于任何比较,总生存期均未见差异。总之,嘌呤类似物,特别是与环磷酰胺联合使用,可显著改善无进展生存期,但不能改善生存期。一些群体,如老年人,可能看不到相同的益处,最大剂量可能对所有治疗都很重要,包括苯丁酸氮芥。应鼓励对试验进行更长的随访、一致的定义和详细的报告。

著录项

相似文献

  • 外文文献
  • 中文文献
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号