A comparison of four leukapheresis methods to harvest an optimal dose of CD34+ cells: A single center experience.


Journal

European journal of haematology
ISSN: 1600-0609
Titre abrégé: Eur J Haematol
Pays: England
ID NLM: 8703985

Informations de publication

Date de publication:
Dec 2022
Historique:
revised: 22 08 2022
received: 18 03 2022
accepted: 22 08 2022
pubmed: 29 8 2022
medline: 15 11 2022
entrez: 28 8 2022
Statut: ppublish

Résumé

Chemokine receptor CXCR4 antagonist plerixafor (Px) as well as high volume (HV) leukapheresis have been shown to reduce hematopoietic stem progenitor cell (HSPC) mobilization failure rates. However, no direct comparisons of such methods currently exists. We compared the HSPC collection yield based on basal peripheral blood CD34+ cell numbers in patients diagnosed with multiple myeloma or non-Hodgkin's lymphoma undergoing autologous stem cell transplantation in a retrospective chart review. The leukapheresis methods used included HV versus regular volume (RV) with or without Px. There were 116 patients in the study group while the historical control group had 34 patients. Control group underwent RV leukapheresis without Px. Addition of Px or HV in the study group failed to display significant improvement in CD34+ cell collection yield; however, when basal CD34+ cell numbers were taken into account, both Px + RV and HV without Px increased CD34+ cell collection yield. The collection failure rates of HV without Px group were comparable to Px + RV when the basal CD34+ cell numbers were over 20/μl. Of interest, multivariate linear regression analysis did not detect any significant difference between HV versus Px + RV or other leukapheresis methods in CD34 yields or collection failure rates from a single collection after controlling for other factors (sex, age, or underlying disease). In multivariate analysis, pre apheresis CD34+ cell number was significantly and positively associated with the CD34+ cell yields from a single apheresis. In our studies, the majority of patients can be rescued without Px by HV alone as a potential cost saving approach. In summary, trend in our studies reflects that both Px and HV are capable of reducing the mobilization failure rates except the poorest mobilizers, which will need to be validated in larger studies.

Sections du résumé

BACKGROUND BACKGROUND
Chemokine receptor CXCR4 antagonist plerixafor (Px) as well as high volume (HV) leukapheresis have been shown to reduce hematopoietic stem progenitor cell (HSPC) mobilization failure rates. However, no direct comparisons of such methods currently exists.
METHODS AND MATERIALS METHODS
We compared the HSPC collection yield based on basal peripheral blood CD34+ cell numbers in patients diagnosed with multiple myeloma or non-Hodgkin's lymphoma undergoing autologous stem cell transplantation in a retrospective chart review. The leukapheresis methods used included HV versus regular volume (RV) with or without Px. There were 116 patients in the study group while the historical control group had 34 patients.
RESULTS AND CONCLUSIONS CONCLUSIONS
Control group underwent RV leukapheresis without Px. Addition of Px or HV in the study group failed to display significant improvement in CD34+ cell collection yield; however, when basal CD34+ cell numbers were taken into account, both Px + RV and HV without Px increased CD34+ cell collection yield. The collection failure rates of HV without Px group were comparable to Px + RV when the basal CD34+ cell numbers were over 20/μl. Of interest, multivariate linear regression analysis did not detect any significant difference between HV versus Px + RV or other leukapheresis methods in CD34 yields or collection failure rates from a single collection after controlling for other factors (sex, age, or underlying disease). In multivariate analysis, pre apheresis CD34+ cell number was significantly and positively associated with the CD34+ cell yields from a single apheresis. In our studies, the majority of patients can be rescued without Px by HV alone as a potential cost saving approach. In summary, trend in our studies reflects that both Px and HV are capable of reducing the mobilization failure rates except the poorest mobilizers, which will need to be validated in larger studies.

Identifiants

pubmed: 36030395
doi: 10.1111/ejh.13856
doi:

Substances chimiques

Cyclams 0
Granulocyte Colony-Stimulating Factor 143011-72-7
Heterocyclic Compounds 0
Benzylamines 0
Antigens, CD34 0
Immunologic Factors 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

711-718

Informations de copyright

© 2022 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Références

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Weaver CH, Hazelton B, Birch R, et al. An analysis of engraftment kinetics as a function of the CD34 content of peripheral blood progenitor cell collections in 692 patients after the administration of myeloablative chemotherapy. Blood. 1995;86:3961-3969.
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Auteurs

Yuankai Lin (Y)

Division of Hematology and Oncology, University of Illinois College of Medicine, Chicago, Illinois, USA.

Youngmin Park (Y)

Clinical Stem Cell Laboratory, UI Health, Chicago, Illinois, USA.

Amit Khanal (A)

Division of Hematology and Oncology, University of Illinois College of Medicine, Chicago, Illinois, USA.

Sally Campbell-Lee (S)

Division of Epidemiology and Biostatistics, University of Illinois, Chicago, Illinois, USA.

Li Liu (L)

Division of Epidemiology and Biostatistics, University of Illinois, Chicago, Illinois, USA.
Biorstatistics Shared Resource Center, University of Illinois Cancer Center, Chicago, Illinois, USA.

Zhengjia Chen (Z)

Division of Epidemiology and Biostatistics, University of Illinois, Chicago, Illinois, USA.
Biorstatistics Shared Resource Center, University of Illinois Cancer Center, Chicago, Illinois, USA.

Pritesh Patel (P)

Division of Hematology and Oncology, University of Illinois College of Medicine, Chicago, Illinois, USA.

Vladimir Vidanovic (V)

Division of Epidemiology and Biostatistics, University of Illinois, Chicago, Illinois, USA.

Karen Sweiss (K)

Department of Pharmacy Practice, College of Pharmacy, University of Illinois, Chicago, Illinois, USA.

Grace Irene (G)

Clinical Stem Cell Laboratory, UI Health, Chicago, Illinois, USA.

David Peace (D)

Division of Hematology and Oncology, University of Illinois College of Medicine, Chicago, Illinois, USA.

Damiano Rondelli (D)

Division of Hematology and Oncology, University of Illinois College of Medicine, Chicago, Illinois, USA.

Nadim Mahmud (N)

Division of Hematology and Oncology, University of Illinois College of Medicine, Chicago, Illinois, USA.
Clinical Stem Cell Laboratory, UI Health, Chicago, Illinois, USA.

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Classifications MeSH