Evidence for continued dose escalation of plerixafor for hematopoietic progenitor cell collections in sickle cell disease Research Letter


Authors: Boulad, F.; Zhang, J.; Yazdanbakhsh, K.; Sadelain, M.; Shi, P. A.
Title: Evidence for continued dose escalation of plerixafor for hematopoietic progenitor cell collections in sickle cell disease
Abstract: We present data from our study of plerixafor mobilization (NCT02193191) relevant to the question of whether further dose escalation of plerixafor can address inconsistent adequacy of CD34+ mobilization for gene therapy of sickle cell disease (SCD). We found that, in the same patient, higher plerixafor dosing was associated with higher fold increases in PB CD34+ count, but not necessarily higher absolute CD34+ counts. Variation in pre-apheresis absolute CD34+ counts was related to intra-individual variation in baseline PB CD34+ counts and inter-individual variation in responsiveness to plerixafor. Overall, our results support further studies of continued dose escalation of plerixafor for autologous HPC collection in SCD. © 2021 Elsevier Inc.
Keywords: gene therapy; plerixafor; sickle cell disease; cxcr4; hematopoietic progenitor cell mobilization
Journal Title: Blood Cells, Molecules, and Diseases
Volume: 90
ISSN: 1079-9796
Publisher: Elsevier Inc.  
Date Published: 2021-09-01
Start Page: 102588
Language: English
DOI: 10.1016/j.bcmd.2021.102588
PROVIDER: scopus
PUBMED: 34166998
PMCID: PMC8338885
DOI/URL:
Notes: Article -- Export Date: 1 July 2021 -- Source: Scopus
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  1. Farid Boulad
    329 Boulad
  2. Michel W J Sadelain
    584 Sadelain