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Survival outcomes of children with relapsed or refractory myeloid leukemia associated with Down syndrome.

Authors :
Raghuram N
Hasegawa D
Nakashima K
Rahman S
Antoniou E
Skajaa T
Merli P
Verma A
Rabin KR
Aftandilian C
Kotecha RS
Cheuk D
Jahnukainen K
Kolenova A
Balwierz W
Norton A
O'Brien M
Cellot S
Chopek A
Arad-Cohen N
Goemans B
Rojas-Vasquez M
Ariffin H
Bartram J
Kolb EA
Locatelli F
Klusmann JH
Hasle H
McGuire B
Hasnain A
Sung L
Hitzler J
Source :
Blood advances [Blood Adv] 2023 Nov 14; Vol. 7 (21), pp. 6532-6539.
Publication Year :
2023

Abstract

Children with Down syndrome (DS) are at a significantly higher risk of developing acute myeloid leukemia, also termed myeloid leukemia associated with DS (ML-DS). In contrast to the highly favorable prognosis of primary ML-DS, the limited data that are available for children who relapse or who have refractory ML-DS (r/r ML-DS) suggest a dismal prognosis. There are few clinical trials and no standardized treatment approach for this population. We conducted a retrospective analysis of international study groups and pediatric oncology centers and identified 62 patients who received treatment with curative intent for r/r ML-DS between year 2000 to 2021. Median time from diagnosis to relapse was 6.8 (range, 1.1-45.5) months. Three-year event-free survival (EFS) and overall survival (OS) were 20.9 ± 5.3% and 22.1 ± 5.4%, respectively. Survival was associated with receipt of hematopoietic stem cell transplantation (HSCT) (hazard ratio [HR], 0.28), duration of first complete remission (CR1) (HR, 0.31 for > 12 months) and attainment of remission after relapse (HR, 4.03). Patients who achieved complete remission (CR) before HSCT, had an improved OS and EFS of 56.0 ± 11.8% and 50.5 ± 11.9%, respectively compared to those who underwent HSCT without CR (3-year OS and EFS of 10.0 ± 9.5%). Treatment failure after HSCT was predominantly because of disease recurrence (52%) followed by treatment-related mortality (10%). The prognosis of r/r ML-DS remains dismal even in the current treatment period and serve as a reference point for current prognostication and future interventional studies. Clinical trials aimed at improving the survival of patients with r/r ML-DS are needed.<br /> (Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0), permitting only noncommercial, nonderivative use with attribution. All other rights reserved.)

Details

Language :
English
ISSN :
2473-9537
Volume :
7
Issue :
21
Database :
MEDLINE
Journal :
Blood advances
Publication Type :
Academic Journal
Accession number :
36735769
Full Text :
https://doi.org/10.1182/bloodadvances.2022009381