| Literature DB >> 27442600 |
Samantha Pozzi1, Massimo Gentile2, Stefano Sacchi1, Raffaella Marcheselli1, Alessandro Corso3, Federica Cocito3, Pellegrino Musto4, Attilio Guarini5, Carla Minoia5, Iolanda Vincelli6, Roberto Ria7, Elena Rivolti8, Giuseppe Mele9, Alessia Bari1, Carla Mazzone2, Stefania Badiali1, Luigi Marcheselli1, Antonio Palumbo10, Fortunato Morabito2.
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/m2 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.Entities:
Keywords: Multiple myeloma; bendamustine; clinical trial; lenalidomide
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Year: 2016 PMID: 27442600 DOI: 10.1080/10428194.2016.1205741
Source DB: PubMed Journal: Leuk Lymphoma ISSN: 1026-8022