Comparable Long-Term Outcome after Allogeneic Stem Cell Transplantation from Sibling and Matched Unrelated Donors in Patients with Acute Myeloid Leukemia Older Than 50 Years: A Report on Behalf of the Acute Leukemia Working Party of the European Society for Blood and Marrow Transplantation.


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:
11 2019
Historique:
received: 23 04 2019
revised: 30 05 2019
accepted: 26 06 2019
pubmed: 5 7 2019
medline: 18 8 2020
entrez: 5 7 2019
Statut: ppublish

Résumé

Allogeneic stem cell transplantation (SCT) is potentially curative therapy in acute myeloid leukemia (AML). Marked improvement has been achieved with SCT from matched unrelated donors (MUDs) in recent years. However, there are limited data comparing the long-term outcomes (beyond 10 years) after SCT from sibling donors and MUDs in older patients with AML. We analyzed these outcomes in a large cohort of patients with AML (n = 1134), age ≥50 years, who were alive and leukemia-free 2 years after SCT from matched siblings (n = 848) or MUDs (n = 286), with a median follow-up of 8.9 years. The median age was 56 and 58 years after SCT from siblings and MUDs, respectively (P = .005). In the sibling group, 77%, 12%, and 11% were in first complete remission (CR1), second complete remission (CR2), and active leukemia at SCT compared with 50%, 25%, and 25% in the MUD group, respectively (P < .001). Sixty-one percent of siblings and 62% of MUDs had reduced-intensity conditioning (P = .78). The 10-year leukemia-free survival (LFS) of patients surviving leukemia-free 2 years after SCT was 72% and 62%, respectively (P = .30). Multivariate analysis identified active leukemia at SCT (hazard ratio [HR], 1.86; P = .0001) or CR2 (HR, 1.51; P = .02) compared with CR1, female recipients (HR, 0.71; P = .006), adverse cytogenetics (HR, 2.52; P = .01), and prior graft-versus-host disease (HR, 1.31; P = .04) as independent factors predicting LFS. Donor and conditioning type were not significant. The cumulative incidence was 15% and 17% (P = .97) for late relapse mortality and 13% and 21% for late nonrelapse mortality, respectively (P = .15). In conclusion, long-term LFS is similar, and patients who are leukemia-free 2 years after SCT can expect favorable outcomes with both donor types.

Identifiants

pubmed: 31271887
pii: S1083-8791(19)30415-X
doi: 10.1016/j.bbmt.2019.06.031
pii:
doi:

Types de publication

Clinical Trial Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

2251-2260

Informations de copyright

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

Auteurs

Avichai Shimoni (A)

Chaim Sheba Medical Center, Tel-Hashomer, Tel-Aviv University, Tel-Aviv, Israel. Electronic address: avichai.shimoni@sheba.health.gov.il.

Myriam Labopin (M)

Acute Leukemia Working Party Office, Paris, France.

Bipin Savani (B)

Vanderbilt University Hematology & Transplantation, Nashville, Tennessee.

Michael Byrne (M)

Vanderbilt University Hematology & Transplantation, Nashville, Tennessee.

Liisa Volin (L)

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

Jürgen Finke (J)

Department of Medicine, Hematology, and Oncology, University of Freiburg, Freiburg, Germany.

Dietger Niederwieser (D)

Division of Hematology & Oncology, University Hospital Leipzig, Leipzig, Germany.

Gerhard Ehninger (G)

Medizinische Klinik und Poliklinik I, Universitaetsklinikum Dresden, Dresden, Germany.

Didier Blaise (D)

Programme de Transplantation & Therapie Cellulaire, Centre de Recherche en Cancérologie de Marseille, Institut Paoli Calmettes, Marseille, France.

Dietrich Beelen (D)

Department of Bone Marrow Transplantation, University Hospital, Essen, Germany.

Reza Tabrizi (R)

CHU Bordeaux, Hôpital Haut-leveque, Pessac, France.

Henrik Sengeloev (H)

Bone Marrow Transplant Unit L 4043, National University Hospital, Copenhagen, Denmark.

Arnold Ganser (A)

Department of Hematology, Hemostasis, Oncology, and Stem Cell Transplantation, Hannover Medical School, Hannover, Germany.

Jan J Cornelissen (JJ)

Department of Hematology, Erasmus MC Cancer Institute, University Medical Center Rotterdam, Rotterdam, The Netherlands.

Mohamad Mohty (M)

Service d'Hématologie et de Thérapie cellulaire, Hôpital Saint-Antoine, Paris, France.

Arnon Nagler (A)

Chaim Sheba Medical Center, Tel-Hashomer, Tel-Aviv University, Tel-Aviv, Israel; Acute Leukemia Working Party Office, Paris, France.

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