Impact of allogeneic stem cell transplantation comorbidity indexes after haplotransplant using post-transplant cyclophosphamide.


Journal

Cancer medicine
ISSN: 2045-7634
Titre abrégé: Cancer Med
Pays: United States
ID NLM: 101595310

Informations de publication

Date de publication:
10 2021
Historique:
revised: 11 08 2021
received: 21 04 2021
accepted: 26 08 2021
pubmed: 22 9 2021
medline: 11 3 2022
entrez: 21 9 2021
Statut: ppublish

Résumé

Three different scoring systems have been developed to assess pre-transplant comorbidity in allogeneic hematopoietic stem cell transplantation (Allo-HSCT): the Hematopoietic Cell Transplantation-Specific Comorbidity Index, the Comorbidity/Age index, and the Augmented Comorbidity/Age index. All were devised to predict overall survival (OS) and disease-free survival (DFS) survivals and non-relapse mortality (NRM) in patients receiving HLA-matched Allo-HSCT, but their performance has scarcely been studied in the haploidentical Allo-HSCT setting with post-transplant cyclophosphamide, a procedure in constant expansion worldwide. To address this issue, their impact on survivals and NRM was examined in a cohort of 223 patients treated with haploidentical Allo-HSCT in four different centers. With a median follow-up of 35.6 months, 3-year OS, DFS, and NRM were 48.1% ± 4%, 46.3% ± 4%, and 30.0% ± 3%, respectively. No impact was found for any of the three comorbidity scores in univariate analysis. In multivariate analyses, the only three factors associated with lower OS were DRI (p < 0.001), an older age of recipients (≥55 years old, p = 0.02) and of donors (≥40 years old, p = 0.005). Older donor age was also associated with lower DFS and higher NRM. The comorbidity scores do not predict survivals nor NRM in haploidentical Allo-HSCT with PTCY, suggesting that pre-transplant comorbidities should not be a contra-indication to this procedure.

Sections du résumé

BACKGROUND
Three different scoring systems have been developed to assess pre-transplant comorbidity in allogeneic hematopoietic stem cell transplantation (Allo-HSCT): the Hematopoietic Cell Transplantation-Specific Comorbidity Index, the Comorbidity/Age index, and the Augmented Comorbidity/Age index. All were devised to predict overall survival (OS) and disease-free survival (DFS) survivals and non-relapse mortality (NRM) in patients receiving HLA-matched Allo-HSCT, but their performance has scarcely been studied in the haploidentical Allo-HSCT setting with post-transplant cyclophosphamide, a procedure in constant expansion worldwide.
METHODS
To address this issue, their impact on survivals and NRM was examined in a cohort of 223 patients treated with haploidentical Allo-HSCT in four different centers.
RESULTS
With a median follow-up of 35.6 months, 3-year OS, DFS, and NRM were 48.1% ± 4%, 46.3% ± 4%, and 30.0% ± 3%, respectively. No impact was found for any of the three comorbidity scores in univariate analysis. In multivariate analyses, the only three factors associated with lower OS were DRI (p < 0.001), an older age of recipients (≥55 years old, p = 0.02) and of donors (≥40 years old, p = 0.005). Older donor age was also associated with lower DFS and higher NRM.
CONCLUSION
The comorbidity scores do not predict survivals nor NRM in haploidentical Allo-HSCT with PTCY, suggesting that pre-transplant comorbidities should not be a contra-indication to this procedure.

Identifiants

pubmed: 34547182
doi: 10.1002/cam4.4262
pmc: PMC8525117
doi:

Substances chimiques

Cyclophosphamide 8N3DW7272P

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

7194-7202

Informations de copyright

© 2021 The Authors. Cancer Medicine published by John Wiley & Sons Ltd.

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Auteurs

Maxime Jullien (M)

Hematology Department, Nantes University Hospital, Nantes, France.

Corentin Orvain (C)

Hematology Department, Angers University Hospital, 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 (A)

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.

Mathilde Hunault (M)

Hematology Department, Angers University Hospital, 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, Site of Brest, Brest, France.

Gaelle Guillerm (G)

Hematology Department, Brest University Hospital, Brest, France.

Aurelien Giltat (A)

Hematology Department, Angers University Hospital, Angers, France.

Sylvie François (S)

Hematology Department, Angers University Hospital, Angers, France.

Sylvain Thepot (S)

Hematology Department, Angers University Hospital, Angers, France.

Steven Le Gouill (S)

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.

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