| Literature DB >> 32865474 |
Patrick Hagen1, Anita D'Souza2, Parameswaran Hari2, Omar Davila3, Mei-Jie Zhang2, David H Vesole4, Scott E Smith1, Tulio E Rodriguez5, Patrick J Stiff1.
Abstract
Melphalan at a dose of 200 mg/m2 (MEL200) remains the standard high dose therapy before autologous stem cell transplantation (ASCT) for multiple myeloma (MM). Intensifying the high dose regimen has shown promising results. We report here 7-year follow up of our novel high dose regimen of busulfan and melphalan followed by bortezomib (BuMelVel). Forty-three MM patients received BuMelVel high dose therapy with pharmacokinetic adjusted busulfan. Outcomes were compared to a matched control cohort from the CIBMTR database (n = 162) receiving MEL200. The primary endpoint was progression free survival. Five year PFS was 47% v 30% (95% CI; 32-62) in favor or the BuMelVel group (95% CI; 23-37) (p = 0.05). In multivariate analysis for PFS, BuMelVel (HR 0.65; 95% CI 0.44-0.97)(p = 0.036) was predictive. Similar to recent reports of double alkylator therapy, although depth of response was similar between the BuMelVel group and MEL200, the BUMELVEL group experienced an improved PFS.Entities:
Keywords: Multiple myeloma; autologous stem cell transplantation; bortezomib; busulfan; melphalan
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Year: 2020 PMID: 32865474 PMCID: PMC7786301 DOI: 10.1080/10428194.2020.1811275
Source DB: PubMed Journal: Leuk Lymphoma ISSN: 1026-8022