| Literature DB >> 27124703 |
Katja Weisel1, Chantal Doyen2, Meletios Dimopoulos3, Adrian Yee4, Juan José Lahuerta5, Amber Martin6, Karin Travers6, Eric Druyts7, Kabirraaj Toor7, Niels Abildgaard8, Jin Lu9, Jan Van Droogenbroeck10, Catarina Geraldes11, Mario Petrini12, Laurent Voillat13, Eric Voog14, Thierry Facon15.
Abstract
In newly diagnosed multiple myeloma (MM), patients ineligible for front-line autologous stem cell transplantation (ASCT), melphalan and prednisone (MP) with thalidomide (MPT) or bortezomib (VMP) are standard first-line therapeutic options. Despite new treatment regimens incorporating bortezomib or lenalidomide, MM remains incurable. The FIRST study demonstrated significant improvement in progression-free survival (PFS) and overall survival (OS) for the combination of lenalidomide and low-dose dexamethasone (Rd) until progression vs. MPT in transplant-ineligible ndMM patients. However, to date no head-to-head randomized controlled trials (RCTs) have compared Rd or MPT versus VMP. We conducted a network meta-analysis using RCTs identified through a systematic literature review to evaluate the relative efficacy of Rd versus other regimens on survival endpoints in previously untreated MM patients ineligible for ASCT. In this analysis, Rd was associated with a significant PFS and survival advantage versus other first-line treatments (VMP, MPT, MP), challenging the role of alkylators in this setting.Entities:
Keywords: Lenalidomide; multiple myeloma; network meta-analysis; systematic review
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Year: 2016 PMID: 27124703 DOI: 10.1080/10428194.2016.1177772
Source DB: PubMed Journal: Leuk Lymphoma ISSN: 1026-8022