Institute of Hematology 'Seràgnoli', University of Bologna, Bologna, Italy.
Ann Oncol. 2013 Nov;24(11):2892-7. doi: 10.1093/annonc/mdt366. Epub 2013 Sep 12.
Mantle cell lymphoma (MCL) is an uncommon type of non-Hodgkin lymphoma with poor overall prognosis, requiring the development of new therapies. Lenalidomide is an immunomodulatory agent demonstrating antitumor and antiproliferative effects in MCL. We report results from a long-term subset analysis of 57 patients with relapsed/refractory MCL from the NHL-003 phase II multicenter study of single-agent lenalidomide in patients with aggressive lymphoma
Lenalidomide was administered orally 25 mg daily on days 1-21 every 28 days until progressive disease (PD) or intolerability. The primary end point was overall response rate (ORR).
Fifty-seven patients with relapsed/refractory, advanced-stage MCL had a median of three prior therapies. The ORR was 35% [complete response (CR)/CR unconfirmed (CRu) 12%], with a median duration of response (DOR) of 16.3 months (not yet reached in patients with CR/CRu) by blinded independent central review. The median time to first response was 1.9 months. Median progression-free survival was 8.8 months, and overall survival had not yet been reached. The most common grade 3/4 adverse events (AEs) were neutropenia (46%), thrombocytopenia (30%), and anemia (13%).
These results show the activity of lenalidomide in heavily pretreated, relapsed/refractory MCL. Responders had a durable response with manageable side-effects. Clinical trial number posted on www.clinicaltrials.gov NCT00413036.
套细胞淋巴瘤(MCL)是一种罕见的非霍奇金淋巴瘤,总体预后较差,需要开发新的治疗方法。来那度胺是一种免疫调节药物,在 MCL 中具有抗肿瘤和抗增殖作用。我们报告了 NHL-003 期研究中 57 例复发性/难治性 MCL 患者的长期亚组分析结果,该研究是一项评估来那度胺单药治疗侵袭性淋巴瘤患者的 II 期多中心研究。
来那度胺每天口服 25mg,第 1-21 天,每 28 天一次,直到疾病进展(PD)或不耐受。主要终点是总缓解率(ORR)。
57 例复发/难治性、晚期 MCL 患者的中位既往治疗数为 3 次。ORR 为 35%[完全缓解(CR)/未确认的 CR(CRu)12%],盲法独立中心评估的中位缓解持续时间(DOR)为 16.3 个月(CR/CRu 患者尚未达到)。首次缓解的中位时间为 1.9 个月。中位无进展生存期为 8.8 个月,总生存期尚未达到。最常见的 3/4 级不良事件(AE)为中性粒细胞减少(46%)、血小板减少(30%)和贫血(13%)。
这些结果表明来那度胺在既往大量治疗、复发/难治性 MCL 患者中具有活性。缓解者的反应持久且副作用可控。临床试验编号在 www.clinicaltrials.gov 上公布 NCT00413036。