Myeloablative Unrelated Cord Blood Transplantation in Adolescents and Young Adults with Acute Leukemia.


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:
12 2019
Historique:
received: 23 05 2019
revised: 09 07 2019
accepted: 23 07 2019
pubmed: 9 8 2019
medline: 9 9 2020
entrez: 9 8 2019
Statut: ppublish

Résumé

Outcomes for adolescents and young adults (AYAs) with leukemia differ from other age groups and are still under-represented in clinical research. The aim of this study was to analyze outcomes of umbilical cord blood transplant (UCBT) in AYAs with acute leukemia reported to Eurocord/European Society for Blood and Marrow Transplantation. Patients (N = 504) had acute lymphoblastic (59%) or myeloid leukemia (41%), were aged 15 to 25 years, and received UCBT after myeloablative conditioning regimens between 2004 and 2016. The primary endpoint was 3-year overall survival (OS). Median follow-up was 3.9 years. Transplant was single in 58% and double UCBT in 42%. Three-year OS was 45% and leukemia free survival (LFS) was 41%. Cumulative incidence functions (CIFs) of nonrelapse mortality (NRM) and relapse were 31% and 28%, respectively. CIF of acute graft-versus-host disease (GVHD) grades II to IV at day 100 was 28%. Three-year CIF of chronic GVHD was 25%. In adjusted analysis, better disease status at UCBT (hazard ratio [HR], 2.74; P < .001) and more recent UCBT (HR, 1.43; P = .01) were associated with increased OS, and a similar effect of these factors was observed on LFS. Contrastingly, the use of antithymocyte globulin had a negative effect in LFS. The risk of acute GVHD grades II to IV increased with the use of double UCBT (HR, 1.65; P  = .02) and decreased with more recent transplant period (HR, .65; P = .02) and antithymocyte globulin use (HR, .55; P  = .01). Outcomes of AYA UCBT improved in more recent years, becoming comparable with pediatric results. Demonstrating the feasibility of UCBT in AYAs facilitates stem cell source selection and provides the basis for future prospective studies.

Identifiants

pubmed: 31394275
pii: S1083-8791(19)30503-8
doi: 10.1016/j.bbmt.2019.07.031
pii:
doi:

Substances chimiques

Antilymphocyte Serum 0

Types de publication

Clinical Trial Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

2438-2446

Informations de copyright

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

Auteurs

Hiromi Hayashi (H)

Eurocord, Hôpital Saint Louis, Assistance Publique-Hôpitaux de Paris, Université de Paris, Paris, France; Monacord, Centre Scientifique de Monaco, Principauté de Monaco, Monaco; Department of Hematology and Oncology, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

Fernanda Volt (F)

Eurocord, Hôpital Saint Louis, Assistance Publique-Hôpitaux de Paris, Université de Paris, Paris, France; Monacord, Centre Scientifique de Monaco, Principauté de Monaco, Monaco.

Jaime Sanz (J)

Hospital Universitario La Fe, Valencia, Spain.

Eefke Petersen (E)

University Medical Centre, Utrecht, The Netherlands.

Nathalie Dhedin (N)

Hematology for Adolescents and Young Adults Unit, Hôpital Saint-Louis, Paris, France.

Rachael Hough (R)

University College London, London, United Kingdom.

Noel Milpied (N)

Hospital Haut-Lévêque, Bordeaux, France.

Emanuele Angelucci (E)

Hematology and Transplant Center, Istituto di Ricovero e Cura a Carattere Scientifico Ospedale Policlinico San Martino, Genova, Italy.

Ibrahim Yakoub-Agha (I)

Centre hospitalier universitaire de Lille, Lille Inflammation Research International Center, Institut national de la santé et de la recherche médical U995, Université de Lille, Lille, France.

Mauricette Michallet (M)

Service d'Hematologie, Centre Léon Bérard, Lyon, France.

Gerard Michel (G)

Hôpital de la Timone Enfant, Marseille, France.

Mahmoud Aljurf (M)

King Faisal Specialist Hospital & Research Centre, Riyadh, Saudi Arabia.

Chantal Kenzey (C)

Eurocord, Hôpital Saint Louis, Assistance Publique-Hôpitaux de Paris, Université de Paris, Paris, France; Monacord, Centre Scientifique de Monaco, Principauté de Monaco, Monaco.

Vanderson Rocha (V)

Eurocord, Hôpital Saint Louis, Assistance Publique-Hôpitaux de Paris, Université de Paris, Paris, France; Monacord, Centre Scientifique de Monaco, Principauté de Monaco, Monaco.

Jean-Hugues Dalle (JH)

Hôpital Universitaire Robert-Debré, Paris, France; Paediatric Disease Working Party of European Society for Blood and Marrow Transplantation.

Peter Bader (P)

Paediatric Disease Working Party of European Society for Blood and Marrow Transplantation; Goethe-Universität Frankfurt am Main, Frankfurt, Germany.

Annalisa Ruggeri (A)

Eurocord, Hôpital Saint Louis, Assistance Publique-Hôpitaux de Paris, Université de Paris, Paris, France; Monacord, Centre Scientifique de Monaco, Principauté de Monaco, Monaco; Ospedale Pediatrico Bambino Gesù, Rome, Italy; Cellular Therapy & Immunobiology Working Party of European Society for Blood and Marrow Transplantation.

Eliane Gluckman (E)

Eurocord, Hôpital Saint Louis, Assistance Publique-Hôpitaux de Paris, Université de Paris, Paris, France; Monacord, Centre Scientifique de Monaco, Principauté de Monaco, Monaco. Electronic address: eliane.gluckman@gmail.com.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH