Suppr超能文献

苯达莫司汀、低剂量地塞米松和来那度胺(BdL)用于治疗复发/难治性多发性骨髓瘤患者的I/II期研究证实了非常有前景的结果。

Bendamustine, Low-dose dexamethasone, and lenalidomide (BdL) for the treatment of patients with relapsed/refractory multiple myeloma confirms very promising results in a phase I/II study.

作者信息

Pozzi Samantha, Gentile Massimo, Sacchi Stefano, Marcheselli Raffaella, Corso Alessandro, Cocito Federica, Musto Pellegrino, Guarini Attilio, Minoia Carla, Vincelli Iolanda, Ria Roberto, Rivolti Elena, Mele Giuseppe, Bari Alessia, Mazzone Carla, Badiali Stefania, Marcheselli Luigi, Palumbo Antonio, Morabito Fortunato

机构信息

a Department of Diagnostic, Clinical Medicine and Public Health Medicine , University of Modena and Reggio Emilia , Modena , Italy.

b Department of Hemato-Oncology , Cosenza Hospital , Cosenza , Italy.

出版信息

Leuk Lymphoma. 2017 Mar;58(3):552-559. doi: 10.1080/10428194.2016.1205741. Epub 2016 Jul 21.

Abstract

Lenalidomide and dexamethasone are an effective treatment for naïve and relapsed multiple myeloma (MM) patients. Bendamustine is a good option for B-cell malignancies showing only partial cross resistance with alkylating agents used in MM patients. Based on these considerations, we proposed a phase I/II study testing escalating doses of bendamustine and lenalidomide and fixed low doses of dexamethasone (BdL). Fifteen patients were enrolled in phase I study. Maximum tolerated dose was established at dose "level 0": bendamustine 40 mg/m days 1,2; lenalidomide 10 mg days 1-21; d 40 mg days 1,8,15,22 every 28-day cycle, for six cycles. We enrolled 23 patients in the phase II study. BdL combination showed mainly hematological toxicities, fever and infections. Overall response rate was 47%. After median follow up of 22 months, median PFS was 10 months. Two-years OS rate was 65%. BdL combination confirmed to be a promising treatment for patients with relapsed/refractory MM.

摘要

来那度胺和地塞米松是初治及复发的多发性骨髓瘤(MM)患者的有效治疗方案。苯达莫司汀对于仅与MM患者使用的烷化剂有部分交叉耐药的B细胞恶性肿瘤是一个不错的选择。基于这些考虑,我们开展了一项I/II期研究,测试递增剂量的苯达莫司汀和来那度胺以及固定低剂量的地塞米松(BdL)。15名患者参加了I期研究。最大耐受剂量确定为“0级”剂量:苯达莫司汀40mg/m²,第1、2天;来那度胺10mg,第1 - 21天;地塞米松40mg,第1、8、15、22天,每28天为一个周期,共六个周期。我们在II期研究中纳入了23名患者。BdL联合方案主要表现出血液学毒性、发热和感染。总缓解率为47%。中位随访22个月后,中位无进展生存期为10个月。两年总生存率为65%。BdL联合方案被证实是复发/难治性MM患者的一种有前景的治疗方法。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验