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The effects of different schedules of bortezomib, melphalan, and prednisone for patients with newly diagnosed multiple myeloma who are transplant ineligible: a matching-adjusted indirect comparison.

Maria-Victoria Mateos-MantecaJesús San F MiguelHartmut GoldschmidtPieter SonneveldMeletios- Athanasios DimopoulosBart HeegMahmoud HashimWilliam DeraedtPeter HuAnnette LamJianming He
Published in: Leukemia & lymphoma (2019)
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.
Keyphrases
  • multiple myeloma
  • newly diagnosed
  • phase iii
  • study protocol
  • clinical trial
  • free survival
  • phase ii
  • high dose
  • electronic health record
  • open label
  • oxidative stress
  • machine learning
  • big data