Non-cryopreserved hematopoietic stem cells in autograft patients with lymphoma: a matched-pair analysis comparing a single center experience with the use of cryopreserved stem cells reported to the European Society for Blood and Marrow Transplantation registry.


Journal

Cytotherapy
ISSN: 1477-2566
Titre abrégé: Cytotherapy
Pays: England
ID NLM: 100895309

Informations de publication

Date de publication:
06 2021
Historique:
received: 10 10 2020
revised: 02 12 2020
accepted: 28 12 2020
pubmed: 9 3 2021
medline: 16 10 2021
entrez: 8 3 2021
Statut: ppublish

Résumé

Around 50 000 autologous stem cell transplantations are done each year worldwide using cryopreserved peripheral blood stem cells (PBSCs). Cryopreservation is time-consuming and expensive. Since 2007, several retrospective studies have shown that PBSCs can be stored at 4°C for 2-3 days, allowing autologous stem cell transplantation in patients with multiple myeloma receiving high-dose melphalan. Data with non-cryopreserved PBSCs in patients autografted for lymphoma following longer pre-conditioning regimens are limited. In addition, no controlled comparison has been able to detect unforeseen differences. The authors compared outcomes of 94 consecutive adult patients with lymphoma (66 with Hodgkin lymphoma) autografted in our department in Oran (Algeria) using PBSCs stored at 4°C, from 2009 to 2018, with patients receiving cryopreserved stem cells reported to the European Society for Blood and Marrow Transplantation registry. Patients autografted in Oran were matched with patients receiving cryopreserved PBSCs in the registry (four controls per patient in Oran). Neutrophil engraftment was significantly faster with cryopreserved PBSCs (P = 0.003). By day 10, only 17% of patients receiving non-cryopreserved PBSCs engrafted versus 48% for cryopreserved PBSCs. Likewise, platelet recovery to 20 000/mm This analysis suggests that, in patients with lymphoma receiving pre-transplant regimens such as carmustine, etoposide, cytarabine and melphalan, PBSCs stored at 4°C for up to 6 days can be used safely in centers with no cryopreservation facility. However, the kinetics of hematopoietic recovery showed a significant, albeit small, delay in engraftment for both neutrophils and platelets, which favors the use of cryopreservation if available.

Sections du résumé

BACKGROUND AIMS
Around 50 000 autologous stem cell transplantations are done each year worldwide using cryopreserved peripheral blood stem cells (PBSCs). Cryopreservation is time-consuming and expensive. Since 2007, several retrospective studies have shown that PBSCs can be stored at 4°C for 2-3 days, allowing autologous stem cell transplantation in patients with multiple myeloma receiving high-dose melphalan. Data with non-cryopreserved PBSCs in patients autografted for lymphoma following longer pre-conditioning regimens are limited. In addition, no controlled comparison has been able to detect unforeseen differences.
METHODS
The authors compared outcomes of 94 consecutive adult patients with lymphoma (66 with Hodgkin lymphoma) autografted in our department in Oran (Algeria) using PBSCs stored at 4°C, from 2009 to 2018, with patients receiving cryopreserved stem cells reported to the European Society for Blood and Marrow Transplantation registry. Patients autografted in Oran were matched with patients receiving cryopreserved PBSCs in the registry (four controls per patient in Oran).
RESULTS
Neutrophil engraftment was significantly faster with cryopreserved PBSCs (P = 0.003). By day 10, only 17% of patients receiving non-cryopreserved PBSCs engrafted versus 48% for cryopreserved PBSCs. Likewise, platelet recovery to 20 000/mm
CONCLUSIONS
This analysis suggests that, in patients with lymphoma receiving pre-transplant regimens such as carmustine, etoposide, cytarabine and melphalan, PBSCs stored at 4°C for up to 6 days can be used safely in centers with no cryopreservation facility. However, the kinetics of hematopoietic recovery showed a significant, albeit small, delay in engraftment for both neutrophils and platelets, which favors the use of cryopreservation if available.

Identifiants

pubmed: 33678598
pii: S1465-3249(21)00007-4
doi: 10.1016/j.jcyt.2020.12.016
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

483-487

Informations de copyright

Copyright © 2021 International Society for Cell & Gene Therapy. All rights reserved.

Auteurs

Mohamed-Amine Bekadja (MA)

Department of Hematology and Cell Therapy, Oran, Algeria.

Ariane Boumendil (A)

European Society for Blood and Marrow Transplantation Global Committee, Paris, France.

Didier Blaise (D)

Institut Paoli Calmettes, Cancer Research Center of Marseille, Aix Marseille University, Marseille, France.

Patrice Chevallier (P)

Department of Hematology and Cell Therapy, Centre Hospitalier Universitaire, Nantes, France.

Karl S Peggs (KS)

University College London Cancer Institute, London, UK.

Gilles Salles (G)

Department of Hematology and Cell Therapy, Hospices Civils, Lyon, France.

Sebastian Giebel (S)

Maria Sklodowska-Curie National Research Institute of Oncology, Gliwice, Poland.

Reinhard Marks (R)

University of Freiburg, Freiburg, Germany.

William Arcese (W)

Policlinico Universitario Tor Vergata, Rome, Italy.

Noel Milpied (N)

Department of Hematology and Stem Cell Transplantation, Centre Hospitalier Universitaire, Bordeaux, France.

Herve Finel (H)

European Society for Blood and Marrow Transplantation Global Committee, Paris, France.

Norbert Claude Gorin (NC)

European Society for Blood and Marrow Transplantation Global Committee, Paris, France; Department of Hematology and Cell Therapy, Hôpital Saint-Antoine, Sorbonne University, Paris, France. Electronic address: gorinclaude@gmail.com.

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