Impact of in vivo T-cell depletion in patients with myelodysplastic syndromes undergoing allogeneic hematopoietic stem cell transplant: a registry study from the Chronic Malignancies Working Party of the EBMT.


Journal

Bone marrow transplantation
ISSN: 1476-5365
Titre abrégé: Bone Marrow Transplant
Pays: England
ID NLM: 8702459

Informations de publication

Date de publication:
05 2022
Historique:
received: 09 09 2020
accepted: 14 02 2022
revised: 18 03 2021
pubmed: 28 2 2022
medline: 14 5 2022
entrez: 27 2 2022
Statut: ppublish

Résumé

While in vivo T-cell depletion (TCD) is widely used, its benefit in patients with MDS still remains a matter of debate. This study evaluates the impact of TCD on outcomes, and compares ATG and alemtuzumab, in patients with MDS. 1284 patients from the EBMT registry were included in this study with 470 patients in the no-TCD group and 814 in the TCD group (alemtuzumab N = 168; ATG N = 646). At 6 months, aGVHD III-IV cumulative incidences (CI) for no-TCD, ATG or alemtuzumab groups were 13% vs 14% vs 11% (ns), respectively. At 5 years, CI of chronic GVHD were 64% vs 52% vs 51% (p < 0.00017); and CI of relapse was 23% vs 25% vs 39% (p < 0.0001) for no TCD, ATG and alemtuzumab respectively; OS was 47% vs 46% vs 34% (p = 0.009) respectively; and GRFS was 21% vs 28% and 20% (p = 0.045) respectively. In multivariable analysis, ATG improved GRFS, and alemtuzumab decreased OS. Both ATG and alemtuzumab decreased risk of chronic GVHD, but the increased risk of relapse with alemtuzumab is associated with a poor GRFS and suggest to not use alemtuzumab in the setting of allo-SCT for high risk disease.

Identifiants

pubmed: 35220412
doi: 10.1038/s41409-022-01620-x
pii: 10.1038/s41409-022-01620-x
doi:

Substances chimiques

Alemtuzumab 3A189DH42V

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

768-774

Informations de copyright

© 2022. The Author(s), under exclusive licence to Springer Nature Limited.

Références

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Auteurs

Edouard Forcade (E)

CHU Bordeaux, F-33000, Bordeaux, France.

Sylvie Chevret (S)

Hopital Saint-Louis, APHP, Université de Paris, Paris, France.

Jürgen Finke (J)

Department of Medicine I, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.

Gerhard Ehninger (G)

Universitaetsklinikum Dresden, Dresden, Germany.

Francis Ayuk (F)

University Hospital Eppendorf, Hamburg, Germany.

Dietrich Beelen (D)

University Hospital, Essen, Germany.

Linda Koster (L)

EBMT Data Office, Leiden, The Netherlands.

Arnold Ganser (A)

Hannover Medical School, Hannover, Germany.

Liisa Volin (L)

HUCH Comprehensive Cancer Center, Helsinki, Finland.

Henrik Sengeloev (H)

Rigshospitalet, Copenhagen, Denmark.

Mauricette Michallet (M)

Centre Hospitalier Lyon Sud, Lyon, France.

Johanna Tischer (J)

University Hospital, LMU Munich, Department of Medicine III, Munich, Germany.

Pavel Jindra (P)

Charles University Hospital, Pilsen, Czech Republic.

Maria Jesús Pascual Cascon (MJP)

Hospital Regional de Málaga, Málaga, Spain.

Yener Koc (Y)

Medical Park Hospitals, Antalya, Turkey.

Mutlu Arat (M)

Sisli Florence Nightingale Hospital, Istanbul, Turkey.

Agnieszka Tomaszewska (A)

Department of Hematology, Oncology and Internal Medicine, Medical University of Warsaw, Warsaw, Poland.

Patrick Hayden (P)

St James Hospital, Dublin, Ireland.

Theo de Witte (T)

Radboud University - Nijmegen Medical Centre, Nijmegen, The Netherlands.

Ibrahim Yakoub-Agha (I)

CHU de Lille, université de Lille, LIRIC, Inserm U995, 59000, Lille, France.

Nicolaus Kröger (N)

University Hospital Eppendorf, Hamburg, Germany.

Marie Robin (M)

Hopital Saint-Louis, APHP, Université de Paris, Paris, France. marie.robin@aphp.fr.

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