Peripheral Blood Stem Cells versus Bone Marrow for T Cell-Replete Haploidentical Transplantation with Post-Transplant Cyclophosphamide in Hodgkin Lymphoma.


Journal

Biology of blood and marrow transplantation : journal of the American Society for Blood and Marrow Transplantation
ISSN: 1523-6536
Titre abrégé: Biol Blood Marrow Transplant
Pays: United States
ID NLM: 9600628

Informations de publication

Date de publication:
09 2019
Historique:
received: 14 03 2019
revised: 09 05 2019
accepted: 17 05 2019
pubmed: 28 5 2019
medline: 30 7 2020
entrez: 26 5 2019
Statut: ppublish

Résumé

Haploidentical stem cell transplantation (haplo-SCT) with post-transplant cyclophosphamide (PT-Cy) represents a potential curative strategy for patients with Hodgkin lymphoma (HL) when a matched related or unrelated donor is not available. The role of graft source, either bone marrow (BM) or peripheral blood stem cells (PBSCs), in this setting has not been fully elucidated. We performed a retrospective study on 91 patients with HL to compare the outcome after BM (n = 53) or PBSC (n = 38) transplant. Eighty-nine patients engrafted with no difference between BM and PBSCs in terms of median time for neutrophil (20 versus 20 days, P = .405) and platelet (26 versus 26.5 days, P = .994) engraftment. With a median follow-up of 40.2 months, 100-day cumulative incidences of grades II to IV acute graft-versus host disease (GVHD) and grades II to IV acute GVHD were 24% and 4%, respectively. Graft source was not associated with a different risk of acute GVHD both by univariate and multivariate analyses. Consistently, 1-year cumulative incidence of chronic GVHD was 7% with no differences between the 2 graft types (P = .761). Two-year rates of overall survival (OS), progression-free survival (PFS), nonrelapse mortality, and GVHD/relapse-free survival (GRFS) were 67%, 58%, 20%, and 52%, respectively. By univariate analysis, pretransplant disease status was the main variable affecting all outcomes. By multivariate analysis, PBSCs resulted in a protective factor for OS (hazard ratio [HR], .29; P = .006), PFS (HR, .38; P = .001), and GRFS (HR, .44; P = .020). The other independent variables affecting the final outcome were pretransplant disease status and hematopoietic cell transplant-specific comorbidity index. In conclusion, when planning a haplo-SCT with PT-Cy for patients with poor-risk HL, graft type is an important variable to take into account when selecting the best available donor.

Identifiants

pubmed: 31128326
pii: S1083-8791(19)30328-3
doi: 10.1016/j.bbmt.2019.05.017
pii:
doi:

Substances chimiques

Cyclophosphamide 8N3DW7272P

Types de publication

Clinical Trial Comparative Study Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

1810-1817

Informations de copyright

Copyright © 2019 American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. All rights reserved.

Auteurs

Jacopo Mariotti (J)

Bone Marrow Transplant Unit, Humanitas Clinical and Research Center, Rozzano, Italy. Electronic address: jacopo.mariotti@cancercenter.humanitas.it.

Raynier Devillier (R)

Department of Hematology, Transplantation Program, Institut Paoli Calmettes, Marseille, France.

Stefania Bramanti (S)

Bone Marrow Transplant Unit, Humanitas Clinical and Research Center, Rozzano, Italy.

Laura Giordano (L)

Division of Biostatistics, Department of Oncology, Humanitas Clinical and Research Center, Rozzano, Italy.

Barbara Sarina (B)

Bone Marrow Transplant Unit, Humanitas Clinical and Research Center, Rozzano, Italy.

Sabine Furst (S)

Department of Hematology, Transplantation Program, Institut Paoli Calmettes, Marseille, France.

Angela Granata (A)

Department of Hematology, Transplantation Program, Institut Paoli Calmettes, Marseille, France.

Valerio Maisano (V)

Department of Hematology, Transplantation Program, Institut Paoli Calmettes, Marseille, France.

Thomas Pagliardini (T)

Department of Hematology, Transplantation Program, Institut Paoli Calmettes, Marseille, France.

Chiara De Philippis (C)

Bone Marrow Transplant Unit, Humanitas Clinical and Research Center, Rozzano, Italy.

Maria Kogan (M)

Bone Marrow Transplant Unit, Humanitas Clinical and Research Center, Rozzano, Italy.

Catherine Faucher (C)

Department of Hematology, Transplantation Program, Institut Paoli Calmettes, Marseille, France.

Samia Harbi (S)

Department of Hematology, Transplantation Program, Institut Paoli Calmettes, Marseille, France.

Christian Chabannon (C)

Cell Therapy Unit, Institut Paoli Calmettes, Marseille, France; Aix-Marseille Université, Marseille, France; Centre de Recherche en Cancérologie de Marseille, Marseille, France.

Carmelo Carlo-Stella (C)

Bone Marrow Transplant Unit, Humanitas Clinical and Research Center, Rozzano, Italy; Department of Medical Biotechnology and Translational Medicine, University of Milano, Milano, Italy.

Reda Bouabdallah (R)

Department of Hematology, Transplantation Program, Institut Paoli Calmettes, Marseille, France.

Armando Santoro (A)

Bone Marrow Transplant Unit, Humanitas Clinical and Research Center, Rozzano, Italy; Humanitas University, Humanitas Clinical and Research Hospital, Rozzano, Italy.

Didier Blaise (D)

Department of Hematology, Transplantation Program, Institut Paoli Calmettes, Marseille, France; Cell Therapy Unit, Institut Paoli Calmettes, Marseille, France; Aix-Marseille Université, Marseille, France.

Luca Castagna (L)

Bone Marrow Transplant Unit, Humanitas Clinical and Research Center, Rozzano, Italy.

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