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Review
. 2023 Aug 24;50(5):438-447.
doi: 10.1159/000531940. eCollection 2023 Oct.

Mobilization Strategies in Myeloma Patients Intended for Autologous Hematopoietic Cell Transplantation

Affiliations
Review

Mobilization Strategies in Myeloma Patients Intended for Autologous Hematopoietic Cell Transplantation

Esa Jantunen et al. Transfus Med Hemother. .

Abstract

Background: Multiple myeloma is currently the leading indication for autologous hematopoietic cell transplantation (AHCT). A prerequisite for AHCT is mobilization and collection of adequate blood graft to support high-dose therapy. Current mobilization strategies include granulocyte colony-stimulating factor (G-CSF) alone or in combination with chemotherapy most commonly cyclophosphamide (CY). More recently, plerixafor has become into agenda especially in patients who mobilize poorly. In the selection of a mobilization method, several factors should be considered.

Summary: Preplanned collection target is important as G-CSF plus plerixafor is more effective in the mobilization of CD34+ cells than G-CSF alone. On the other hand, CY plus G-CSF is superior to G-CSF only mobilization. Previous therapy and age of the patients are important considerations as G-CSF alone may not be effective enough in patients with risk factors for poor mobilization. These factors include extensive lenalidomide exposure, irradiation to bone marrow-bearing sites, higher age, or a previous mobilization failure. Also, local preferences and experiences as well as the number of apheresis needed are important issues as well as cost-effectiveness considerations. Mobilization method used may have implication for cellular composition of collected grafts, which might have an impact on posttransplant events such as hematologic and immune recovery in addition to also potential long-term outcomes.

Key message: Currently, G-CSF alone and preemptive plerixafor if needed might be considered as a standard mobilization strategy in MM patients intended for AHCT.

Keywords: CD34+ cells; Graft composition; Granulocyte colony-stimulating factor; Mobilization of blood grafts; Multiple myeloma; Plerixafor.

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Conflict of interest statement

A.P. reports honoraria from Behring and AbbVie and has participated in Scientific Advisory Board meetings organized by AbbVie, Janssen-Cilag, Novartis, and Takeda. V.V. reports consultancy fees from AbbVie, Amgen, Celgene, Janssen-Cilag, Roche, and Sanofi. R.S. has received Janssen-Cilag Research Funding for FMG-MM01 study, Celgene Research Funding for FMG-MM02 study, Celgene/BMS and Takeda Research Funding for NMSG#23/15 study, and Amgen and BMS Research Funding and compensation as a member of the Scientific Advisory Boards organized by Amgen, BMS, Celgene, Janssen-Cilag, and Takeda and consultancy fees from Amgen, Celgene, Janssen-Cilag, and Sanofi. The other authors declare no conflicts of interest.

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