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Haematopoietic cell transplantation for children with acute megakaryoblastic leukaemia without Down syndrome.

Authors :
Hama A
Taga T
Tomizawa D
Muramatsu H
Hasegawa D
Adachi S
Yoshida N
Noguchi M
Sato M
Okada K
Koh K
Mitsui T
Takahashi Y
Miyamura T
Hashii Y
Kato K
Atsuta Y
Okamoto Y
Source :
British journal of haematology [Br J Haematol] 2023 May; Vol. 201 (4), pp. 747-756. Date of Electronic Publication: 2023 Feb 14.
Publication Year :
2023

Abstract

Patients with acute megakaryoblastic leukaemia of Down syndrome (DS-AMKL) have an excellent survival rate; however, patients with non-DS-AMKL experience poor outcomes. Therefore, this study retrospectively analysed 203 children with non-DS-AMKL who underwent their first haematopoietic cell transplantation (HCT) from 1986 to 2015 using a nationwide Japanese HCT registry data to assess HCT outcomes for non-DS-AMKL. The 5-year overall survival (OS) and event-free survival (EFS) rates were 43% and 38% respectively. The 5-year OS rate was significantly higher for patients who underwent HCT in the first complete remission (CR1, 72%) than for those in the second CR (CR2, 23%) and non-CR (16%) (p < 0.001), and for those from a human leukocyte antigen (HLA)-matched (52%) than for those from an HLA-mismatched donor (27%) (p < 0.001). Multivariate analysis for OS revealed that HCT in CR2 and non-CR was a significant risk factor (hazard ratio, 5.86; 95% confidence interval, 3.56-9.53; p < 0.001). The 3-year EFS in patients who received HCT in CR1 using reduced-intensity conditioning (RIC, 35%) was significantly lower than in those using myeloablative conditioning (busulfan-based, 71%; total body irradiation-based, 58%) (p < 0.001). Risk stratification in patients with non-DS-AMKL should be established to determine HCT indication in CR1.<br /> (© 2023 British Society for Haematology and John Wiley & Sons Ltd.)

Details

Language :
English
ISSN :
1365-2141
Volume :
201
Issue :
4
Database :
MEDLINE
Journal :
British journal of haematology
Publication Type :
Academic Journal
Accession number :
36786154
Full Text :
https://doi.org/10.1111/bjh.18691