Suppr超能文献

来那度胺用于多发性骨髓瘤患者干细胞移植后。

Lenalidomide after stem-cell transplantation for multiple myeloma.

机构信息

Blood and Marrow Transplant Program, Roswell Park Cancer Institute, Buffalo, NY 14263, USA.

出版信息

N Engl J Med. 2012 May 10;366(19):1770-81. doi: 10.1056/NEJMoa1114083.

Abstract

BACKGROUND

Data are lacking on whether lenalidomide maintenance therapy prolongs the time to disease progression after autologous hematopoietic stem-cell transplantation in patients with multiple myeloma.

METHODS

Between April 2005 and July 2009, we randomly assigned 460 patients who were younger than 71 years of age and had stable disease or a marginal, partial, or complete response 100 days after undergoing stem-cell transplantation to lenalidomide or placebo, which was administered until disease progression. The starting dose of lenalidomide was 10 mg per day (range, 5 to 15).

RESULTS

The study-drug assignments were unblinded in 2009, when a planned interim analysis showed a significantly longer time to disease progression in the lenalidomide group. At unblinding, 20% of patients who received lenalidomide and 44% of patients who received placebo had progressive disease or had died (P<0.001); of the remaining 128 patients who received placebo and who did not have progressive disease, 86 crossed over to lenalidomide. At a median follow-up of 34 months, 86 of 231 patients who received lenalidomide (37%) and 132 of 229 patients who received placebo (58%) had disease progression or had died. The median time to progression was 46 months in the lenalidomide group and 27 months in the placebo group (P<0.001). A total of 35 patients who received lenalidomide (15%) and 53 patients who received placebo (23%) died (P=0.03). More grade 3 or 4 hematologic adverse events and grade 3 nonhematologic adverse events occurred in patients who received lenalidomide (P<0.001 for both comparisons). Second primary cancers occurred in 18 patients who received lenalidomide (8%) and 6 patients who received placebo (3%).

CONCLUSIONS

Lenalidomide maintenance therapy, initiated at day 100 after hematopoietic stem-cell transplantation, was associated with more toxicity and second cancers but a significantly longer time to disease progression and significantly improved overall survival among patients with myeloma. (Funded by the National Cancer Institute; ClinicalTrials.gov number, NCT00114101.).

摘要

背景

关于来那度胺维持疗法是否能延长多发性骨髓瘤患者自体造血干细胞移植后疾病进展的时间,目前的数据尚不清楚。

方法

在 2005 年 4 月至 2009 年 7 月期间,我们将 460 名年龄小于 71 岁、干细胞移植后 100 天疾病稳定或有边缘性、部分缓解或完全缓解的患者随机分为来那度胺组或安慰剂组,接受来那度胺或安慰剂治疗,直至疾病进展。来那度胺的起始剂量为每天 10mg(5-15mg 范围)。

结果

2009 年进行了计划中的中期分析,结果显示来那度胺组疾病进展时间明显延长,此时研究药物的分配情况被揭盲。揭盲时,接受来那度胺的患者中有 20%和接受安慰剂的患者中有 44%出现疾病进展或死亡(P<0.001);在其余 128 名未出现疾病进展且接受安慰剂的患者中,86 名交叉接受来那度胺治疗。中位随访 34 个月时,接受来那度胺的 231 名患者中有 86 名(37%)和接受安慰剂的 229 名患者中有 132 名(58%)出现疾病进展或死亡。来那度胺组的中位进展时间为 46 个月,安慰剂组为 27 个月(P<0.001)。接受来那度胺的 35 名患者(15%)和接受安慰剂的 53 名患者(23%)死亡(P=0.03)。接受来那度胺的患者更常发生 3 级或 4 级血液学不良事件和 3 级非血液学不良事件(两者比较均 P<0.001)。接受来那度胺的 18 名患者(8%)和接受安慰剂的 6 名患者(3%)发生第二原发癌。

结论

在造血干细胞移植后 100 天开始接受来那度胺维持治疗可导致更多的毒性和第二原发癌,但可显著延长多发性骨髓瘤患者的疾病进展时间和显著改善总生存期。(国家癌症研究所资助;ClinicalTrials.gov 编号,NCT00114101。)

相似文献

引用本文的文献

本文引用的文献

8
Multiple myeloma.多发性骨髓瘤
N Engl J Med. 2011 Mar 17;364(11):1046-60. doi: 10.1056/NEJMra1011442.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验