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Published in: Irish Journal of Medical Science (1971 -) 4/2015

01-12-2015 | Original Article

Child and adolescent Down syndrome-associated leukaemia: the Irish experience

Authors: C. O’Rafferty, J. Kelly, L. Storey, C. Ryan, A. O’Marcaigh, O. Smith

Published in: Irish Journal of Medical Science (1971 -) | Issue 4/2015

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Abstract

Background

Down syndrome (DS), the most common syndromic chromosomal abnormality is associated with a unique susceptibility to develop both acute myeloid (ML) and lymphoblastic leukaemia (ALL). These leukaemias differ from the non-DS-related types of leukaemia and are thought to be distinct biological entities.

Aims

To perform a retrospective review of our experience of treating DS-related leukaemia at Our Lady’s Children’s Hospital.

Methods

Data were extracted from a database established in 2000 to prospectively gather data on DS-associated leukaemias and their outcomes following polychemotherapy. Kaplan–Meier survival curves were constructed.

Results

Nineteen patients with DS-ML were treated and 19 with DS-ALL. Sixteen (84 %) patients with DS-ML are alive and in complete remission with a median follow-up of 7 years. All deaths in this cohort were due to treatment-related mortality (TRM). Of the DS-ALL patients, 12 (63 %) remain alive with a median follow-up of 3.6 years. TRM accounted for five of the six deaths. One death was due to leukaemic relapse.

Conclusion

High cure rates are seen in DS-ML using contemporary polychemotherapy protocols, however, there is significant TRM in this cohort. DS-ALL does not have the same high cure rate as non-DS-ALL (>90 %) and again this is mainly due to an excess of TRM.
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Metadata
Title
Child and adolescent Down syndrome-associated leukaemia: the Irish experience
Authors
C. O’Rafferty
J. Kelly
L. Storey
C. Ryan
A. O’Marcaigh
O. Smith
Publication date
01-12-2015
Publisher
Springer London
Published in
Irish Journal of Medical Science (1971 -) / Issue 4/2015
Print ISSN: 0021-1265
Electronic ISSN: 1863-4362
DOI
https://doi.org/10.1007/s11845-014-1212-2

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