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Bendamustine + rituximab chemoimmunotherapy and maintenance lenalidomide in relapsed refractory chronic lymphocytic leukemia and small lymphocytic lymphoma: A Wisconsin Oncology Network Study

机译:苯达莫司汀+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:威斯康星州肿瘤学网络研究

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摘要

Bendamustine + rituximab (BR) has demonstrated high response rates in relapsed/refractory (R/R) chronic lymphocytic leukemia (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-day cycles of lenalidomide 5-10 mg/day. The primary endpoint was PFS. The median age was 67 years, with a median of 2 prior therapies. Eleven 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 due to primarily hematologic 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 ().
机译:苯达莫司汀+利妥昔单抗(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)<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名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5-10 mg /天的十二个28天周期。主要终点是PFS。中位年龄为67岁,中位为2种既往疗法。十一位已确认存在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例(56%)患者接受来那度胺维持治疗;只有6例患者完成了预期的12个周期,这突出表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。观察到的中位PFS为18.3个月,与未经维持治疗的R / R CLL / SLL中BR诱导的中位值无明显差异(15.2个月)。来那度胺维持治疗在一线治疗中可能更可行,更有效,该治疗正在进行中()。

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