Early Post-Transplantation Serum Ferritin Level Predicts Survival in Recipients of Haploidentical Stem Cell Transplantation Using Post-Transplantation Cyclophosphamide as Graft-versus-Host Disease Prophylaxis.

Age Allogeneic hematopoietic stem cell transplantation Disease Risk Index Ferritin Haploidentical Post-transplantation cyclophosphamide

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:
10 2021
Historique:
received: 20 04 2021
revised: 30 06 2021
accepted: 30 06 2021
pubmed: 11 7 2021
medline: 21 10 2021
entrez: 10 7 2021
Statut: ppublish

Résumé

The negative impact of high serum ferritin level (SFL) before and after allogeneic hematopoietic cell transplantation (allo-HSCT) on outcomes is well recognized. However, it is poorly documented in adults undergoing haploidentical HSCT (haplo-HSCT) with post-transplantation cyclophosphamide (PTCY) for hematologic malignancies. The main objective was to assess the impact of pretransplantation and post-transplantation SFL on overall survival (OS), disease-free survival (DFS), and nonrelapse mortality (NRM) in patients undergoing haplo-HSCT with PTCY. The secondary objective was to identify factors associated with outcomes after transplantation by comparing SFL with other parameters related to the status of patients or donors. This multicentric retrospective study included 223 consecutive patients who underwent haplo-HSCT with PTCY in 4 French centers (Nantes, Angers, Besançon, and Brest) between October 2013 and January 2020. The impact of SFL on OS, DFS, and NRM at different time points was assessed based on receiver operating characteristic curves. With a median follow-up of 37.6 months (interquartile range, 23.5 to 51.0 months), 3-year OS, DFS, and NRM were 48.1 ± 4%, 46.3 ± 4%, and 30.0 ± 3%, respectively. Pretransplantation SFL had no impact on outcomes irrespective of the cutoff tested. Considering patients alive at 3 months post-transplantation, an SFL ≥3500 µg/L at 3 months was statistically significantly associated with worse 3-year OS (32.7 ± 8.7% versus 53.4 ± 7.2%; P = .01) and DFS (30.1 ± 8.2% versus 53.1 ± 7.1%; P = .008), with a trend toward higher NRM (33.2 ± 8.6% versus 17.6 ± 5.4%; P = .10). Similarly, high SFL (≥2700 µg/L) at 6 months post-transplantation was associated with worse 3-year OS (56.1 ± 9.1% versus 79.2 ± 6.0%; P = .02) and DFS (53.6 ± 8.7% versus 74.9 ± 6.2%; P = .01), with a trend toward higher NRM (21.4 ± 7.4% versus 8.2 ± 4.0%; P = .10). In multivariate analysis, high 3-month and 6-month FL remained associated with lower OS and DFS, with a trend toward higher NRM. Pretransplantation SFL appears to have no impact on outcomes in haplo-HSCT with PTCY, in contrast to what is documented in the matched allo-HSCT setting. In contrast, in the haplo-HSCT setting, high SFL early post-transplantation is associated with lower survival and a trend toward higher NRM.

Identifiants

pubmed: 34245928
pii: S2666-6367(21)01035-6
doi: 10.1016/j.jtct.2021.06.032
pii:
doi:

Substances chimiques

Cyclophosphamide 8N3DW7272P
Ferritins 9007-73-2

Types de publication

Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

861.e1-861.e7

Informations de copyright

Copyright © 2021 The American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. All rights reserved.

Auteurs

Maxime Jullien (M)

Hematology Department, Nantes University Hospital, Nantes, France.

Corentin Orvain (C)

Hematology Department, Angers University Hospital, Angers, France; INSERM, CRCINA, University of Angers, Angers, France.

Ana Berceanu (A)

Hematology Department, Besançon University Hospital, Besançon, France.

Marie-Anne Couturier (MA)

Hematology Department, Brest University Hospital, Brest, France.

Thierry Guillaume (T)

Hematology Department, Nantes University Hospital, Nantes, France.

Pierre Peterlin (P)

Hematology Department, Nantes University Hospital, Nantes, France.

Alice Garnier (A)

Hematology Department, Nantes University Hospital, Nantes, France.

Amandine Le Bourgeois (AL)

Hematology Department, Nantes University Hospital, Nantes, France.

Marion Klemencie (M)

Hematology Department, Angers University Hospital, Angers, France.

Aline Schmidt (A)

Hematology Department, Angers University Hospital, Angers, France; INSERM, CRCINA, University of Angers, Angers, France.

Mathilde Hunault (M)

Hematology Department, Angers University Hospital, Angers, France; INSERM, CRCINA, University of Angers, Angers, France.

Etienne Daguindau (E)

Hematology Department, Besançon University Hospital, Besançon, France.

Xavier Roussel (X)

Hematology Department, Besançon University Hospital, Besançon, France.

Pascal Delepine (P)

Cell Therapy Unit, Etablissement Français du Sang-Bretagne, Brest, France.

Gaelle Guillerm (G)

Hematology Department, Brest University Hospital, Brest, France.

Aurelien Giltat (A)

Hematology Department, Besançon University Hospital, Besançon, France.

Sylvie François (S)

Hematology Department, Angers University Hospital, Angers, France.

Sylvain Thepot (S)

INSERM, CRCINA, University of Angers, Angers, France.

Steven Le Gouill (SL)

Hematology Department, Nantes University Hospital, Nantes, France; INSERM UMR1232, CRCINA IRS-UN, University of Nantes, Nantes, France.

Marie-C Béné (MC)

INSERM UMR1232, CRCINA IRS-UN, University of Nantes, Nantes, France; Hematology Biology, Nantes University Hospital, Nantes, France.

Patrice Chevallier (P)

Hematology Department, Nantes University Hospital, Nantes, France; INSERM UMR1232, CRCINA IRS-UN, University of Nantes, Nantes, France. Electronic address: patrice.chevallier@chu-nantes.fr.

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