Successful Mobilization of Autologous Hematopoietic Peripheral Blood Stem Cells after Salvage Chemotherapy in Patients with Low CD34 Blood Cell Counts.
Humans
Hematopoietic Stem Cell Mobilization
/ methods
Transplantation, Autologous
Hematopoietic Stem Cell Transplantation
/ methods
Cyclams
Peripheral Blood Stem Cells
/ metabolism
Heterocyclic Compounds
/ pharmacology
Benzylamines
/ therapeutic use
Granulocyte Colony-Stimulating Factor
/ therapeutic use
Antigens, CD34
/ metabolism
Multiple Myeloma
/ therapy
Lymphoma, Non-Hodgkin
/ therapy
Blood Cell Count
Autologous PBSC
CD34+ cell count
Leukapheresis
Mobilization chemotherapy
Plerixafor
Journal
Transplantation and cellular therapy
ISSN: 2666-6367
Titre abrégé: Transplant Cell Ther
Pays: United States
ID NLM: 101774629
Informations de publication
Date de publication:
11 2022
11 2022
Historique:
received:
23
03
2022
revised:
11
08
2022
accepted:
15
08
2022
pubmed:
25
8
2022
medline:
8
11
2022
entrez:
24
8
2022
Statut:
ppublish
Résumé
A major barrier for proceeding to autologous stem cell transplantation (ASCT) is an inability to mobilize and collect an adequate number of peripheral blood (PB) stem cells (PBSC) for the transplant graft. Plerixafor added to granulocyte colony stimulating factor (G-CSF) alone, without prior chemotherapy, significantly improves the mobilization of autologous PBSC in patients with non-Hodgkin lymphoma (NHL) and multiple myeloma (MM). However, the efficacy of plerixafor and the best timing to give the drug to poorly mobilizing patients with very low PB CD34+ cell counts after salvage chemotherapy and G-CSF are not well defined. We hypothesized that PBSC mobilization and collection might be improved in heavily treated patients who mobilized very poorly after salvage chemotherapy and G-CSF by alternating the days of plerixafor administration and leukapheresis. A day of rest between plerixafor doses, while continuing G-CSF, could allow time for some replenishment of the marrow stem/progenitor cell pool before the next mobilization. A retrospective review of collection results in poorly mobilizing patients at our center was undertaken. Three cohorts were identified: those who got every-other-day plerixafor and leukapheresis, those who got sequential plerixafor and leukapheresis and those who got risk adapted plerixafor. Overall, 69% of patients with NHL and MM with PB CD34+ cell counts <5/µL after salvage chemotherapy and G-CSF were ultimately able to collect adequate CD34+ cells to support ASCT using daily plerixafor and leukapheresis. On the alternating plerixafor and leukapheresis schedule, all 17 patients achieved the cumulative CD34+ cell product goals required for ASCT. This positive observation after salvage chemotherapy and G-CSF led to the incorporation at our center of an alternate-day schedule of plerixafor and leukapheresis into our real-time risk adapted strategy for poor mobilizers. © 2023 American Society for Blood and Marrow Transplantation. Published by Elsevier Inc. All rights reserved.
Identifiants
pubmed: 36002104
pii: S2666-6367(22)01558-5
doi: 10.1016/j.jtct.2022.08.017
pii:
doi:
Substances chimiques
Cyclams
0
Heterocyclic Compounds
0
Benzylamines
0
Granulocyte Colony-Stimulating Factor
143011-72-7
Antigens, CD34
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
754-759Commentaires et corrections
Type : CommentIn
Informations de copyright
Copyright © 2022 The American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. All rights reserved.