| Literature DB >> 31953532 |
Thomas Hueso1,2, Thomas Gastinne3,4, Sylvain Garciaz5, Emmanuelle Tchernonog6, Caroline Delette7, René-Olivier Casasnovas8,9, Eric Durot10, Roch Houot11,12, Benoît Tessoulin3,4, Olivier Tournilhac13, Sandra Malak14, Emmanuel Gyan15,16, Luc-Matthieu Fornecker17, Julie Abraham18, Baptiste Delapierre1,2, Frédéric Peyrade19, Richard Lemal13, Rémy Gressin20, Sylvain Chantepie1,2, Cécile Borel21, Rémy Morello22, Krimo Bouabdallah23, Ahmad Ibrahim24, Reda Bouabdallah5, Steven Le Gouill3,4, Gandhi Damaj25,26.
Abstract
The combination of carmustine, etoposide, cytarabine, and melphalan (BEAM) as conditioning regimen prior to autologous stem-cell transplantation (ASCT) remains the standard of care for patients with mantle cell lymphoma (MCL) who are eligible for transplantation. The replacement of carmustine with bendamustine (BeEAM) was described as a promising alternative in non-Hodgkin lymphoma. The aim of this retrospective study was to compare the BeEAM with the BEAM regimen in MCL patients in the frontline setting. Sixty and 108 patients were included in the BeEAM and the BEAM groups, respectively. At 3 years, progression-free survival (PFS) was significantly higher in the BeEAM than in the BEAM group (84% [73-96] vs. 63% [51-79], p = 0.03). The overall survival was not statistically different between the two groups (p = 0.2). In multivariable analysis, BeEAM regimen remained associated with higher PFS (HR = 0.377, 95% CI, 0.146-0.970; p = 0.043). Subgroup analyses in patients treated with prior rituximab-aracytine induction alone showed that BeEAM improved the PFS compared with BEAM regimen (p = 0.04). Despite the high rate of acute renal failure KDIGO III (32%), treatment-related mortality was not increased with the BeEAM regimen. A prospective randomized trial will be necessary to confirm the beneficial effect of the BeEAM regimen in MCL patients undergoing ASCT.Entities:
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Year: 2020 PMID: 31953532 DOI: 10.1038/s41409-020-0783-y
Source DB: PubMed Journal: Bone Marrow Transplant ISSN: 0268-3369 Impact factor: 5.483