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Clinical characteristics and outcome of refractory/relapsed myeloid leukemia in children with Down syndrome.

Authors :
Taga T
Saito AM
Kudo K
Tomizawa D
Terui K
Moritake H
Kinoshita A
Iwamoto S
Nakayama H
Takahashi H
Tawa A
Shimada A
Taki T
Kigasawa H
Koh K
Adachi S
Source :
Blood [Blood] 2012 Aug 30; Vol. 120 (9), pp. 1810-5. Date of Electronic Publication: 2012 Jul 09.
Publication Year :
2012

Abstract

Myeloid leukemia in Down syndrome (ML-DS) is associated with good response to chemotherapy and favorable prognosis. Because little research has been focused on refractory/relapsed (R/R) cases, we conducted a retrospective analysis for R/R ML-DS. Among ML-DS patients diagnosed between 2000 and 2010 in Japan, 26 relapsed (25 in the BM and 1 in the skin), and 3 refractory patients were enrolled. The male/female ratio was 18/11. The median age at initial diagnosis of ML-DS was 2 years, and the median time to relapse was 8.6 months. Each patient initially had been treated with ML-DS-specific protocols. Thirteen of the 26 patients achieved complete remission with various kinds of reinduction chemotherapies; 2 of 8 survived without further recurrence after receiving allogeneic hematopoietic stem cell transplantation, and 4 of 5 maintained complete remissions with chemotherapy alone. Treatment failures mostly were associated with disease progression rather than treatment-related toxicities. The 3-year OS rate was 25.9% ± 8.5%. A longer duration from initial diagnosis to relapse was a significant favorable prognostic factor (P < .0001). We conclude that clinical outcome for patients with R/R ML-DS generally are unfavorable, even in those receiving hematopoietic stem cell transplantation. Novel methods to identify poor prognostic factors for ML-DS are necessary.

Details

Language :
English
ISSN :
1528-0020
Volume :
120
Issue :
9
Database :
MEDLINE
Journal :
Blood
Publication Type :
Academic Journal
Accession number :
22776818
Full Text :
https://doi.org/10.1182/blood-2012-03-414755