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Motixafortide and G-CSF to mobilize hematopoietic stem cells for autologous transplantation in multiple myeloma: a randomized phase 3 trial

Authors :
Zachary D. Crees
Michael P. Rettig
Reyka G. Jayasinghe
Keith Stockerl-Goldstein
Sarah M. Larson
Illes Arpad
Giulio A. Milone
Massimo Martino
Patrick Stiff
Douglas Sborov
Denise Pereira
Ivana Micallef
Gemma Moreno-Jiménez
Gabor Mikala
Maria Liz Paciello Coronel
Udo Holtick
John Hiemenz
Muzaffar H. Qazilbash
Nancy Hardy
Tahir Latif
Irene García-Cadenas
Abi Vainstein-Haras
Ella Sorani
Irit Gliko-Kabir
Inbal Goldstein
Debby Ickowicz
Liron Shemesh-Darvish
Shaul Kadosh
Feng Gao
Mark A. Schroeder
Ravi Vij
John F. DiPersio
Source :
Nature Medicine. 29:869-879
Publication Year :
2023
Publisher :
Springer Science and Business Media LLC, 2023.

Abstract

Autologous hematopoietic stem cell transplantation (ASCT) improves survival in multiple myeloma (MM). However, many individuals are unable to collect optimal CD34+ hematopoietic stem and progenitor cell (HSPC) numbers with granulocyte colony-stimulating factor (G-CSF) mobilization. Motixafortide is a novel cyclic-peptide CXCR4 inhibitor with extended in vivo activity. The GENESIS trial was a prospective, phase 3, double-blind, placebo-controlled, multicenter study with the objective of assessing the superiority of motixafortide + G-CSF over placebo + G-CSF to mobilize HSPCs for ASCT in MM. The primary endpoint was the proportion of patients collecting ≥6 × 106 CD34+ cells kg–1 within two apheresis procedures; the secondary endpoint was to achieve this goal in one apheresis. A total of 122 adult patients with MM undergoing ASCT were enrolled at 18 sites across five countries and randomized (2:1) to motixafortide + G-CSF or placebo + G-CSF for HSPC mobilization. Motixafortide + G-CSF enabled 92.5% to successfully meet the primary endpoint versus 26.2% with placebo + G-CSF (odds ratio (OR) 53.3, 95% confidence interval (CI) 14.12–201.33, P P + HSPC numbers within two apheresis procedures versus placebo + G-CSF while preferentially mobilizing increased numbers of immunophenotypically and transcriptionally primitive HSPCs. Trial Registration: ClinicalTrials.gov, NCT03246529

Details

ISSN :
1546170X and 10788956
Volume :
29
Database :
OpenAIRE
Journal :
Nature Medicine
Accession number :
edsair.doi...........0a69e4c0e0036bff2e542cdd026f0744
Full Text :
https://doi.org/10.1038/s41591-023-02273-z