...
首页> 外文期刊>British Journal of Haematology >Bendamustine plus rituximab chemoimmunotherapy and maintenance lenalidomide in relapsed, refractory chronic lymphocytic leukaemia and small lymphocytic lymphoma: AWisconsin Oncology Network Study
【24h】

Bendamustine plus rituximab chemoimmunotherapy and maintenance lenalidomide in relapsed, refractory chronic lymphocytic leukaemia and small lymphocytic lymphoma: AWisconsin Oncology Network Study

机译:苯达莫司汀联合利妥昔单抗的化学免疫疗法和来那度胺在复发,难治性慢性淋巴细胞白血病和小淋巴细胞淋巴瘤中的治疗:AWisconsin肿瘤网络研究

获取原文
获取原文并翻译 | 示例
           

摘要

Bendamustine+rituximab (BR) has demonstrated high response rates in relapsed/refractory (R/R) chronic lymphocytic leukaemia (CLL) and small lymphocytic lymphoma (SLL). However, progression-free survival (PFS) after BR is <18months. This study was designed to determine if maintenance lenalidomide after BR induction could improve PFS in R/R CLL/SLL. Thirty-four patients with R/R CLL/SLL who had received 1-5 prior chemotherapy regimens were treated with 6 cycles of BR induction. Patients achieving at least a minor response received twelve 28-d cycles of lenalidomide 5-10mg/d. The primary endpoint was PFS. The median age was 67years, with a median of 2 prior therapies. Eleven patients had confirmed presence of 17p and/or 11q deletions. Twenty-five (74%) completed 6 cycles of induction BR (response rate 56%). Nineteen (56%) patients received maintenance lenalidomide; only 6 patients completed the intended 12 cycles, highlighting the limited feasibility of lenalidomide in this setting, primarily due to haematological and infectious toxicities. The observed median PFS of 183months is not significantly different from that of BR induction in R/R CLL/SLL without maintenance therapy (152months). It is possible that lenalidomide maintenance may be more feasible and effective in the front-line setting, which is being tested in an ongoing trial (NCT01754857).
机译:Bendamustine + rituximab(BR)在复发/难治性(R / R)慢性淋巴细胞性白血病(CLL)和小淋巴细胞性淋巴瘤(SLL)中显示出高应答率。但是,BR后的无进展生存期(PFS)小于18个月。本研究旨在确定BR诱导后维持来那度胺是否可以改善R / R CLL / SLL中的PFS。接受过1-5次化疗方案的34例R / R CLL / SLL患者接受了6个周期的BR诱导治疗。达到至少轻微反应的患者接受来那度胺5-10mg / d的十二个28天周期。主要终点是PFS。中位年龄为67岁,中位有2种先前疗法。确认有11名患者存在17p和/或11q缺失。二十五(74%)人完成了6个诱导性BR周期(反应率56%)。 19名(56%)患者接受来那度胺维持治疗;只有6名患者完成了预期的12个周期,这主要说明来那度胺在这种情况下的可行性有限,这主要是由于血液学和感染毒性。在没有维持治疗的情况下,R / R CLL / SLL中观察到的183个月PFS中值与BR诱导的中值无显着差异。来那度胺维持治疗在前线治疗中可能更为可行和有效,该治疗正在进行中(NCT01754857)。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
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