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Lenalidomide in Pretreated Mantle Cell Lymphoma Patients: An Italian Observational Multicenter Retrospective Study in Daily Clinical Practice (the Lenamant Study)

机译:Lenalidomide在预处理的地幔细胞淋巴瘤患者:日常临床实践中的意大利观察多中心回顾性研究(烯醇研究)

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Abstract Background Mantle cell lymphoma (MCL) has the worst prognosis of B‐cell subtypes owing to its aggressive clinical disease course and incurability with standard chemo‐immunotherapy. Options for relapsed MCL are limited, although several single agents have been studied. Lenalidomide is available in Italy for patients with MCL based on a local disposition of the Italian Drug Agency. Subjects, Materials, and Methods An observational retrospective study was conducted in 24 Italian hematology centers with the aim to improve information on effectiveness and safety of lenalidomide use in real practice. Results Seventy patients received lenalidomide for 21/28 days with a median of eight cycles. At the end of therapy, there were 22 complete responses (31.4%), 11 partial responses, 6 stable diseases, and 31 progressions, with an overall response rate of 47.1%. Eighteen patients (22.9%) received lenalidomide in combination with either dexamethasone ( n ?=?13) or rituximab ( n ?=?5). Median overall survival (OS) was reached at 33 months and median disease‐free survival (DFS) at 20 months: 14/22 patients are in continuous complete response with a median of 26 months. Patients who received lenalidomide alone were compared with patients who received lenalidomide in combination: OS and DFS did not differ. Progression‐free survivals are significantly different: at 56 months, 36% in the combination group versus 13% in patients who received lenalidomide alone. Toxicities were manageable, even if 17 of them led to an early drug discontinuation. Conclusion Lenalidomide therapy for relapsed MCL patients is effective and tolerable even in a real‐life context. Implication for Practice Several factors influence treatment choice in relapsed/refractory mantle cell lymphoma (rrMCL), and the therapeutic scenario is continuously evolving. In fact, rrMCL became the first lymphoma for which four novel agents have been approved: temsirolimus, lenalidomide, ibrutinib, and bortezomib. The rrMCL therapeutic algorithm is not so well established because data in the everyday clinical practice are still poor. Lenalidomide for rrMCL patients is effective and tolerable even in a real‐life context.
机译:摘要背景披风细胞淋巴瘤(MCL)由于其具有侵略性临床疾病课程和与标准化疗免疫疗法而耐用而具有最严重的B细胞亚型预后。虽然已经研究了几种单一药剂,所重复的MCL的选项是有限的。 Lenalidomide在意大利提供了基于意大利药品局的当地处置的MCL患者。受试者,材料和方法在24种意大利血液中心进行了观察回顾性研究,其目的是改善实际实践中番三种胺类使用的有效性和安全性的信息。结果七十名患者接受了Lenalidomide 21/28天,中位数为8个循环。在治疗结束时,有22例完全反应(31.4%),11分歧,6个稳定性疾病和31个进展,总体反应率为47.1%。十八名患者(22.9%)与地塞米松(n?= 13)或rituximab(n?=Δ5)组合接受Lenalidomide。在33个月内达到中位数总生存(OS),20个月内达到中位病残存活(DFS):14/22名患者与26个月的中位数持续完全完全反应。单独接受Lenalidomide的患者与接受Lenalidomide组合的患者进行比较:OS和DFS没有差异。无进展的幸存者显着不同:56个月,组合组与单独接受Lenalidomide的患者的组合组与13%的36%。毒性是可管理的,即使其中17人导致早期药物停药。结论转发MCL患者的Lenalidomide治疗即使在现实生活中也是有效和耐受性。实施实践的含义若干因素影响复发/难治性搭腔细胞淋巴瘤(RRMCL)中的治疗选择,治疗情况不断发展。事实上,RRMCL成为第一个已批准的四种新试剂的淋巴瘤:Temsirolimus,Lenalidomide,Ibrutinib和Bortezomib。 RRMCC治疗算法不太建立,因为日常临床实践中的数据仍然很差。即使在现实生活环境中,RRMCL患者的Lenalidomide也是有效和可容忍的。

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