Back to Search Start Over

Improved Outcome in Young Children Compared to Adolescents and Adults After Allogeneic Hematopoietic Stem Cell Transplant for Acute Myeloid Leukemia: a Retrospective Study From Francophone Society of Bone Marrow Transplantation and Cell Therapy (SFGM-TC) (SFGM-TC)

Authors :
Cécile POCHON
Marie Detrait
Jean-Hugues Dalle
Gérard Michel
Nathalie Dhédin
Yves Chalandon
Eolia Brissot
Edouard Forcade
Anne Sirvent
Faezeh Izzadifar-Legrand
Mauricette Michallet
Cécile Renard
Ibrahim Yakoub-Agha
Fanny Gonzales
Jacques- Olivier Bay
Justyna Kanold
Jérome Cornillon
Claude Eric Bulabois
Marie Angoso
Stéphanie Nguyen
Hélène Labussière-Wallet
Patrice Chevallier
Fanny Rialland
Ali Bazarbachi
Yves Beguin
Anne Huynh
Anne-Lise Ménard
Pascale Schneider
Bénédicte Neven
Catherine Paillard
Nicole Raus
Eliane Albuisson
Thomas Remen
Marie-Thérèse Rubio
Publication Year :
2021
Publisher :
Research Square Platform LLC, 2021.

Abstract

Background: There are currently few data on the outcome of acute myeloid leukemia (AML) in adolescents and young adults (AYAs) after allogeneic HSCT. The aim of this study is to describe the outcome and its specific risk factors for children, AYAs and adults after a first allogeneic HSCT for AML. Methods: In this retrospective study, we compared the outcome of AML patients receiving a first allogeneic HSCT between 2005 and 2017 according to their age at transplantation’s time: children (Results: With a median follow-up of 4.37 years (min-max 0.18 – 14.73 years), the probability of 2 year-overall survival (OS) was 71.4% in children, 61.1% in AYAs and 62.9% in adults (p=0.0009 for intergroup difference). Both relapse and non-relapse mortality (NRM) Cumulative Incidence (CI) estimated at 2 years were different between the age groups (30.8% for children, 35.2% for AYAs and 29.4% for adults - p=0.0254, and 7.0% for children, 10.6% for AYAs and 14.2% for adults, pConclusion: Age is an independent risk factor for NRM and extensive chronic GVHD. This study suggests that AYAs AML patients should be treated with chemotherapy-based MAC regimen and bone marrow as stem cells source.

Details

Database :
OpenAIRE
Accession number :
edsair.doi...........c4b713b5f610fe0f54afdf761188d24e
Full Text :
https://doi.org/10.21203/rs.3.rs-718867/v1