Chang Julie E, Havighurst Thomas, Kim KyungMann, Eickhoff Jens, Traynor Anne M, Kirby-Slimp Rachel, Volk Lynn M, Werndli Jae, Go Ronald S, Weiss Matthias, Blank Jules, Kahl Brad S
Department of Medicine, University of Wisconsin School of Medicine and Public Health and the UW Carbone Cancer Center, Madison, WI, USA.
Department of Biostatistics and Medical Informatics, University of Wisconsin, Madison, WI, USA.
Br J Haematol. 2016 Apr;173(2):283-91. doi: 10.1111/bjh.13957. Epub 2016 Feb 23.
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 <18 months. 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 5-10 mg/d. The primary endpoint was PFS. The median age was 67 years, 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 18·3 months is not significantly different from that of BR induction in R/R CLL/SLL without maintenance therapy (15·2 months). 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).
苯达莫司汀联合利妥昔单抗(BR)已在复发/难治性(R/R)慢性淋巴细胞白血病(CLL)和小淋巴细胞淋巴瘤(SLL)中显示出高缓解率。然而,BR治疗后的无进展生存期(PFS)<18个月。本研究旨在确定BR诱导治疗后使用来那度胺维持治疗是否能改善R/R CLL/SLL患者的PFS。34例接受过1-5线既往化疗方案的R/R CLL/SLL患者接受6个周期的BR诱导治疗。至少达到微小缓解的患者接受12个28天周期的来那度胺治疗,剂量为5-10mg/d。主要终点为PFS。中位年龄为67岁,既往治疗的中位次数为2次。11例患者确诊存在17p和/或11q缺失。25例(74%)完成了6个周期的诱导BR治疗(缓解率为56%)。19例(56%)患者接受来那度胺维持治疗;只有6例患者完成了预定的12个周期,这突出了来那度胺在这种情况下的可行性有限,主要是由于血液学和感染性毒性。观察到的中位PFS为18.3个月,与未进行维持治疗的R/R CLL/SLL患者的BR诱导治疗的中位PFS(15.2个月)无显著差异。来那度胺维持治疗在一线治疗中可能更可行且有效,目前正在进行的一项试验(NCT01754857)中对此进行测试。