Impact of adjunct cytogenetic abnormalities for prognostic stratification in patients with myelodysplastic syndrome and deletion 5q.

Details

Ressource 1Download: 20882045.pdf (780.06 [Ko])
State: Public
Version: Author's accepted manuscript
License: Not specified
Serval ID
serval:BIB_BD04315DCC0E
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Impact of adjunct cytogenetic abnormalities for prognostic stratification in patients with myelodysplastic syndrome and deletion 5q.
Journal
Leukemia
Author(s)
Mallo M., Cervera J., Schanz J., Such E., García-Manero G., Luño E., Steidl C., Espinet B., Vallespí T., Germing U., Blum S., Ohyashiki K., Grau J., Pfeilstöcker M., Hernández J.M., Noesslinger T., Giagounidis A., Aul C., Calasanz M.J., Martín M.L., Valent P., Collado R., Haferlach C., Fonatsch C., Lübbert M., Stauder R., Hildebrandt B., Krieger O., Pedro C., Arenillas L., Sanz M.Á., Valencia A., Florensa L., Sanz G.F., Haase D., Solé F.
ISSN
1476-5551 (Electronic)
ISSN-L
0887-6924
Publication state
Published
Issued date
2011
Peer-reviewed
Oui
Volume
25
Number
1
Pages
110-120
Language
english
Notes
Publication types: Journal Article ; Multicenter Study ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov'tPublication Status: ppublish
Abstract
This cooperative study assessed prognostic factors for overall survival (OS) and risk of transformation to acute myeloid leukemia (AML) in 541 patients with de novo myelodysplastic syndrome (MDS) and deletion 5q. Additional chromosomal abnormalities were strongly related to different patients' characteristics. In multivariate analysis, the most important predictors of both OS and AML transformation risk were number of chromosomal abnormalities (P<0.001 for both outcomes), platelet count (P<0.001 and P=0.001, respectively) and proportion of bone marrow blasts (P<0.001 and P=0.016, respectively). The number of chromosomal abnormalities defined three risk categories for AML transformation (del(5q), del(5q)+1 and del(5q)+ ≥ 2 abnormalities) and two for OS (one group: del(5q) and del(5q)+1; and del(5q)+ ≥ 2 abnormalities, as the other one); with a median survival time of 58.0 and 6.8 months, respectively. Platelet count (P=0.001) and age (P=0.034) predicted OS in patients with '5q-syndrome'. This study demonstrates the importance of additional chromosomal abnormalities in MDS patients with deletion 5q, challenges the current '5q-syndrome' definition and constitutes a useful reference series to properly analyze the results of clinical trials in these patients.
Keywords
Adult, Aged, Aged, 80 and over, Anemia, Macrocytic/genetics, Anemia, Macrocytic/mortality, Chromosome Aberrations, Chromosome Deletion, Chromosomes, Human, Pair 5/genetics, Female, Humans, Karyotyping, Male, Middle Aged, Myelodysplastic Syndromes/genetics, Myelodysplastic Syndromes/mortality, Prognosis, Retrospective Studies
Pubmed
Web of science
Open Access
Yes
Create date
23/02/2012 14:45
Last modification date
20/08/2019 16:31
Usage data