| Literature DB >> 31686561 |
Maria-Victoria Mateos1, Jesus San-Miguel2, Hartmut Goldschmidt3, Pieter Sonneveld4, Meletios A Dimopoulos5, Bart Heeg6, Mahmoud Hashim6, William Deraedt7, Peter Hu8, Annette Lam9, Jianming He9.
Abstract
For patients with newly diagnosed multiple myeloma (NDMM) who are transplant ineligible, bortezomib-melphalan-prednisone (VMP) demonstrated superior efficacy based on the VISTA trial. In subsequent trials, twice-weekly bortezomib was limited to the first cycle or completely replaced with once-weekly bortezomib to reduce toxicity. Following a systematic literature review, the efficacy and safety of modified VMP schedules (pooled data from the once-weekly bortezomib VMP arm of the GIMEMA trial and the VMP arm of the ALCYONE trial) were compared to the VISTA schedule using naïve and unanchored matching-adjusted indirect comparison (MAIC). Median progression-free survival was similar between VISTA and modified VMP (20.7 months [95% CI, 18.4-24.3] vs 19.6 months [95% CI, 18.8-21.0]). Peripheral neuropathy was significantly reduced with modified VMP versus VISTA VMP (all grades: naïve, 32.1% vs 46.8% and MAIC, 32.1% vs 46.7%; both p < .0001). These findings support a modified VMP dosing schedule for patients with NDMM who are transplant ineligible.Entities:
Keywords: VMP; matching-adjusted indirect comparison; multiple myeloma
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Year: 2019 PMID: 31686561 DOI: 10.1080/10428194.2019.1675881
Source DB: PubMed Journal: Leuk Lymphoma ISSN: 1026-8022