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Exploratory analysis of intensified conditioning as first line treatment for patients with high risk multiple myeloma.

Authors :
Bommier C
Talbot A
Harel S
Cuccuini W
Gérard L
Arnulf B
Source :
Hematological oncology [Hematol Oncol] 2020 Oct; Vol. 38 (4), pp. 517-522. Date of Electronic Publication: 2020 Jul 29.
Publication Year :
2020

Abstract

Multiple myeloma has extremely heterogeneous outcomes. Among prognostic factors, t(4;14) and del(17p) are rare oncogenic events associated with very poor prognosis. In an exploratory case-control study, we compared the combination of Busulfan-Melphalan or TBI-Melphalan with high dose Melphalan as a conditioning regimen in a series of 48 patients with del(17p) or t(4;14). These regimens were preceded by a Bortezomib-containing induction. Progression-free survival (PFS) was the primary endpoint whereas overall survival (OS) and complete response (CR) rate were the secondary endpoints. Twenty consecutive cases of high-risk myeloma received a reinforced conditioning regimen of Busulfan 0.8 mg/kg x4/j IV from day-6 to day-3 pre- graft (BuMel) or total body irradiation (TBI) 12 Gy (TbiMel), having received Melphalan 140 mg/m <superscript>2</superscript> at day-2 pre-graft. These cases were matched to 28 controls treated with Melphalan 200 mg/m <superscript>2</superscript> at day-2 (Mel200). After intensification ± consolidation, with a median follow-up of 6.3 years, the CR rate was higher in the BuMel/TbiMel group (65% vs 50%, P = .006). No differences were observed between both groups in terms of PFS and OS (P = .96). PFS in patients with a del(17p) mutation tended to be superior in the BuMel/TbiMel group. Our exploratory study shows that reinforcing the intensification regimen with Busulfan or TBI does not seem to improve the prognosis associated to t(4;14) and del(17p) abnormalities.<br /> (© 2020 John Wiley & Sons Ltd.)

Details

Language :
English
ISSN :
1099-1069
Volume :
38
Issue :
4
Database :
MEDLINE
Journal :
Hematological oncology
Publication Type :
Academic Journal
Accession number :
32569436
Full Text :
https://doi.org/10.1002/hon.2767