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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:来那度胺在预处理的套细胞淋巴瘤患者中的应用:每日临床实践中的意大利多中心观察性回顾性研究(Lenamant研究)

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Background. Mantle cell lymphoma (MCL) has the worst prognosis of Ba??cell subtypes owing to its aggressive clinical disease course and incurability with standard chemoa??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 (na??=a??13) or rituximab (na??=a??5). Median overall survival (OS) was reached at 33 months and median diseasea??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. Progressiona??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 reala??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 reala??life context.
机译:背景。幔细胞淋巴瘤(MCL)的Ba ??细胞亚型预后最差,原因是其侵袭性的临床病程和标准的化学疗法免疫疗法无法治愈。尽管已经研究了几种单一药物,但复发性MCL的选择是有限的。根据意大利药物管理局的当地情况,来那度胺在意大利可用于MCL患者。主题,材料和方法。在意大利的24个血液学中心进行了一项观察性回顾性研究,目的是在实际操作中改善来那度胺使用的有效性和安全性信息。结果。 70名患者接受来那度胺治疗21/28天,中位值为8个周期。在治疗结束时,有22例完全缓解(31.4%),11例部分缓解,6种稳定疾病和31种进展,总缓解率为47.1%。 18名患者(22.9%)接受来那度胺联合地塞米松(na ?? = a ?? 13)或利妥昔单抗(na ?? = a ?? 5)联合治疗。在33个月时达到中位总体生存期(OS),在20个月时达到中值无病生存期(DFS):14/22患者持续完全缓解,中位值为26个月。将单独接受来那度胺的患者与接受来那度胺联合治疗的患者进行比较:OS和DFS无差异。无进展生存率显着不同:在56个月时,联合治疗组为36%,而接受来那度胺的患者为13%。毒性是可以控制的,即使其中17种导致了早期停药。结论。来那度胺治疗复发的MCL患者即使在现实生活中也有效且可耐受。对实践的启示。多种因素影响复发/难治性套细胞淋巴瘤(rrMCL)的治疗选择,并且治疗方案正在不断发展。实际上,rrMCL成为了首个被批准使用四种新型药物的患者:西罗莫司,来那度胺,依鲁替尼和硼替佐米。由于日常临床实践中的数据仍然很差,因此无法很好地建立rrMCL治疗算法。来那度胺对rrMCL患者即使在现实生活中也是有效且可耐受的。

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