Post-transplant cyclophosphamide versus antithymocyte globulin in patients with acute myeloid leukemia in first complete remission undergoing allogeneic stem cell transplantation from 10/10 HLA-matched unrelated donors.


Journal

Journal of hematology & oncology
ISSN: 1756-8722
Titre abrégé: J Hematol Oncol
Pays: England
ID NLM: 101468937

Informations de publication

Date de publication:
03 07 2020
Historique:
received: 18 05 2020
accepted: 23 06 2020
entrez: 5 7 2020
pubmed: 6 7 2020
medline: 18 5 2021
Statut: epublish

Résumé

Graft-versus-host disease (GVHD) remains a major contributor to mortality and morbidity after allogeneic stem-cell transplantation (allo-HSCT). The updated recommendations suggest that rabbit antithymocyte globulin or anti-T-lymphocyte globulin (ATG) should be used for GVHD prophylaxis in patients undergoing matched-unrelated donor (MUD) allo-HSCT. More recently, using post-transplant cyclophosphamide (PTCY) in the haploidentical setting has resulted in low incidences of both acute (aGVHD) and chronic GVHD (cGVHD). Therefore, the aim of our study was to compare GVHD prophylaxis using either PTCY or ATG in patients with acute myeloid leukemia (AML) who underwent allo-HSCT in first remission (CR1) from a 10/10 HLA-MUD. Overall, 174 and 1452 patients from the EBMT registry receiving PTCY and ATG were included. Cumulative incidence of aGVHD and cGVHD, leukemia-free survival, overall survival, non-relapse mortality, cumulative incidence of relapse, and refined GVHD-free, relapse-free survival were compared between the 2 groups. Propensity score matching was also performed in order to confirm the results of the main analysis RESULTS: No statistical difference between the PTCY and ATG groups was observed for the incidence of grade II-IV aGVHD. The same held true for the incidence of cGVHD and for extensive cGVHD. In univariate and multivariate analyses, no statistical differences were observed for all other transplant outcomes. These results were also confirmed using matched-pair analysis. These results highlight that, in the10/10 HLA-MUD setting, the use of PTCY for GVHD prophylaxis may provide similar outcomes to those obtained with ATG in patients with AML in CR1.

Sections du résumé

BACKGROUND
Graft-versus-host disease (GVHD) remains a major contributor to mortality and morbidity after allogeneic stem-cell transplantation (allo-HSCT). The updated recommendations suggest that rabbit antithymocyte globulin or anti-T-lymphocyte globulin (ATG) should be used for GVHD prophylaxis in patients undergoing matched-unrelated donor (MUD) allo-HSCT. More recently, using post-transplant cyclophosphamide (PTCY) in the haploidentical setting has resulted in low incidences of both acute (aGVHD) and chronic GVHD (cGVHD). Therefore, the aim of our study was to compare GVHD prophylaxis using either PTCY or ATG in patients with acute myeloid leukemia (AML) who underwent allo-HSCT in first remission (CR1) from a 10/10 HLA-MUD.
METHODS
Overall, 174 and 1452 patients from the EBMT registry receiving PTCY and ATG were included. Cumulative incidence of aGVHD and cGVHD, leukemia-free survival, overall survival, non-relapse mortality, cumulative incidence of relapse, and refined GVHD-free, relapse-free survival were compared between the 2 groups. Propensity score matching was also performed in order to confirm the results of the main analysis RESULTS: No statistical difference between the PTCY and ATG groups was observed for the incidence of grade II-IV aGVHD. The same held true for the incidence of cGVHD and for extensive cGVHD. In univariate and multivariate analyses, no statistical differences were observed for all other transplant outcomes. These results were also confirmed using matched-pair analysis.
CONCLUSION
These results highlight that, in the10/10 HLA-MUD setting, the use of PTCY for GVHD prophylaxis may provide similar outcomes to those obtained with ATG in patients with AML in CR1.

Identifiants

pubmed: 32620146
doi: 10.1186/s13045-020-00923-0
pii: 10.1186/s13045-020-00923-0
pmc: PMC7333262
doi:

Substances chimiques

Antilymphocyte Serum 0
Immunosuppressive Agents 0
Cyclophosphamide 8N3DW7272P
thymoglobulin D7RD81HE4W

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

87

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Auteurs

Eolia Brissot (E)

Sorbonne Université, AP-HP, INSERM UMRs938, Paris, France. eolia.brissot@aphp.fr.
Service d'Hématologie clinique et de Thérapie cellulaire, Assistance Publique-Hôpitaux de Paris, Hôpital Saint-Antoine, 184, rue du Faubourg Saint Antoine, 75012, Paris, France. eolia.brissot@aphp.fr.

Myriam Labopin (M)

European Society for Blood and Marrow Transplantation Paris Study Office/CEREST-TC, Paris, France.

Ian Moiseev (I)

R.M. Gorbacheva Memorial Institute of Oncology, Hematology and Transplantation, Pavlov First Saint Petersburg State Medical University, St. Petersburg, Russian Federation.

J J Cornelissen (JJ)

Department of Hematology, Erasmus University Medical Center, Rotterdam, the Netherlands.

Ellen Meijer (E)

Amsterdam University Medical Center, VU Medical Center, Department of Hematology, Cancer Center Amsterdam, Amsterdam, Netherlands.

Gwendolyn Van Gorkom (G)

Dept. Internal Medicine, Hematology/Oncology, University Hospital Maastricht, Maastricht, The Netherlands.

Montserrat Rovira (M)

Apheresis & Cellular Therapy Unit, Department of Hemotherapy and Hemostasis, ICMHO, Hospital Clínic, University of Barcelona, Barcelona, Spain.

Fabio Ciceri (F)

Hematology and Bone Marrow Transplantation, IRCCS San Raffaele Scientific Institute, Milan, Italy.
University Vita-Salute San Raffaele, Milan, Italy.

Laimonas Griskevicius (L)

Hematology, Oncology & Transfusion Center, Vilnius University Hospital Santaros Klinikos, Vilnius University, Vilnius, Lithuania.

Didier Blaise (D)

Centre de Recherche en Cancérologie de Marseille, Institut Paoli Calmettes, Marseille, France.

Edouard Forcade (E)

CHU Bordeaux, Hospital Haut-Leveque, Pessac, France.

Martin Mistrik (M)

Department of Haematology and Transfusion Medicine, University Hospital and Comenius University, Bratislava, Slovak Republic.

Stephan Mielke (S)

Department of Internal Medicine II, University Hospital of Würzburg, Oberdürrbacher Str. 6, D-97080, Würzburg, Germany.

Claude Eric Bulabois (CE)

Department of Hematology, CHU de Grenoble, Grenoble, France.

Riitta Niittyvuopio (R)

HUCH Comprehensive Cancer Center, Stem Cell Transplantation Unit, Helsinki, Finland.

Eric Deconinck (E)

Service d'Hématologie, Hopital Jean Minjoz, Besançon, France.

Annalisa Ruggeri (A)

Hematology and Bone Marrow Transplantation, IRCCS San Raffaele Scientific Institute, Milan, Italy.
University Vita-Salute San Raffaele, Milan, Italy.

Jaime Sanz (J)

Department of Haematology, University Hospital La Fe, University of Valencia, Valencia, Spain.
Department of Haematology, Centro de Investigación Biomédica en Red de Cáncer, Instituto Carlos III, Madrid, Spain.

Alexandros Spyridonidis (A)

Department of Internal Medicine, Bone Marrow Transplantation Unit, University Hospital of Patras, Patras, Greece.

Bipin Savani (B)

Long Term Transplant Clinic, Vanderbilt University Medical Center, Nashville, TN, USA.

Sebastian Giebel (S)

Department of Bone Marrow Transplantation and Oncohematology, Maria Sklodowska-Curie Memorial Cencer Center and Institute of Oncology, Gliwice, Poland.

Arnon Nagler (A)

Hematology Division, BMT and Cord Blood Bank, Chaim Sheba Medical Center, Tel-Hashomer, Israel.

Mohamad Mohty (M)

Sorbonne Université, AP-HP, INSERM UMRs938, Paris, France.
Service d'Hématologie clinique et de Thérapie cellulaire, Assistance Publique-Hôpitaux de Paris, Hôpital Saint-Antoine, 184, rue du Faubourg Saint Antoine, 75012, Paris, France.

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