Institute of Haematology and Medical Oncology "L. e A. Seràgnoli," University of Bologna, Italy.
Clin Lymphoma Myeloma Leuk. 2011 Dec;11(6):462-6. doi: 10.1016/j.clml.2011.02.001. Epub 2011 May 4.
Diffuse large B-cell lymphoma (DLBCL) is the most common subtype of aggressive non-Hodgkin lymphoma and despite recent chemotherapeutic advances up to half of all patients relapse. Here we report the results from a phase 2, single-arm, single-center trial evaluating the safety and efficacy of lenalidomide plus rituximab in elderly patients with relapsed or refractory DLBCL.
Between March and June 2009, elderly patients (65 years of age or older) with relapsed/refractory DLBCL who had been heavily pretreated were recruited. Oral lenalidomide (20 mg/d for 21 days of each 28-day cycle) was initiated for four cycles and rituximab (375 mg/m(2)) was administered on day 1 and day 21 of each 28-day cycle for four cycles. After this induction phase, patients achieving a complete response (CR), partial response (PR), or stable disease (SD) were given lenalidomide maintenance therapy at the same schedule for another 8 months.
A total of 23 patients with a median of three prior treatments (range, 2 to 8) were included. The overall response rate (CR + PR) at the end of the induction phase was 35% (n = 8). Ten patients (7 CR, 1 PR, and 2 SD patients) were eligible for lenalidomide maintenance and 8 of these patients achieved a CR. Adverse events were manageable and the most common included neutropenia and thrombocytopenia.
Oral lenalidomide in combination with rituximab is active in elderly patients with relapsed/refractory DLBCL with a high percentage of patients achieving a continuous CR after lenalidomide maintenance.
弥漫性大 B 细胞淋巴瘤(DLBCL)是侵袭性非霍奇金淋巴瘤中最常见的亚型,尽管最近化疗有所进展,但仍有近一半的患者复发。在此,我们报告了一项 2 期、单臂、单中心试验的结果,该试验评估了来那度胺联合利妥昔单抗在复发/难治性 DLBCL 老年患者中的安全性和疗效。
2009 年 3 月至 6 月期间,招募了年龄在 65 岁及以上、经大量预处理后复发/难治性 DLBCL 的老年患者。口服来那度胺(21 天周期的第 1 至 20 天,每天 20mg),共 4 个周期;利妥昔单抗(375mg/m²)在每个 28 天周期的第 1 天和第 21 天给药,共 4 个周期。在诱导期结束后,达到完全缓解(CR)、部分缓解(PR)或疾病稳定(SD)的患者接受相同方案的来那度胺维持治疗,为期 8 个月。
共纳入 23 例患者,中位治疗次数为 3 次(范围为 2 至 8 次)。诱导期结束时的总缓解率(CR+PR)为 35%(n=8)。10 例患者(7 例 CR、1 例 PR 和 2 例 SD 患者)有资格接受来那度胺维持治疗,其中 8 例患者达到 CR。不良事件可管理,最常见的是中性粒细胞减少和血小板减少。
来那度胺联合利妥昔单抗在复发/难治性 DLBCL 老年患者中具有活性,其中很大比例的患者在来那度胺维持治疗后持续达到 CR。