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Monosomal and complex karyotypes as prognostic parameters in patients with International Prognostic Scoring System higher risk myelodysplastic syndrome treated with azacitidine

Authors
Hwang, K.-L.Song, M.-K.Shin, H.-J.Na, H.-J.Shin, D.-H.Kim, J.-K.Moon, J.-H.Ahn, J.-S.Song, I.-C.Hong, J.Lee, G.-W.Chung, J.-S.
Issue Date
2014
Publisher
Korean Society of Hematology
Keywords
Azacitidine; Chromosomal abnormalities; Complex karyotype; Monosomal karyotype; Myelodysplastic syndrome
Citation
Blood Research, v.49, no.4, pp.234 - 240
Journal Title
Blood Research
Volume
49
Number
4
Start Page
234
End Page
240
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/12974
DOI
10.5045/br.2014.49.4.234
ISSN
2287-979X
Abstract
Background Azacitidine (AZA) is standard care for patients with myelodysplastic syndrome (MDS) who have not had allogeneic stem cell transplantation. Chromosomal abnormalities (CA)including complex karyotype (CK) or monosomal karyotype (MK) are associated with clinical outcome in patients with MDS. Methods We investigated which prognostic factors including CAs would predict clinical outcomes in patients with International Prognostic Scoring System (IPSS) higher risk MDS treatedwith AZA, retrospectively. CK was defined as the presence of three or more numerical or structural CAs. MK was defined as the presence of two or more distinct autosomal monosomies or single autosomal monosomy with at least one additional structural CA. Results A total of 243 patients who treated with AZA, were enrolled. CK was present in 124 patientsand MK was present in 90 patients. Bone marrow blasts ≥15% and CK were associated with poorer response (P=0.038, P=0.007) and overall survival (OS) (P>0.001, P >0.001) independently. Although MK in CK group was not associated with prognosis, non-MK status in non-CK group reflected favorable OS (P=0.005). The group including <3 CAs was associated with poorer OS (group including >3 CAs vs. only three CAs, P=0.001; group with <3 CAs vs. only three CAs, P=0.001). Conclusion CK was an important prognostic parameter associated with worse outcome. MK may predict poor survival in only non-CK status. The higher number of CAs was associated with poorer survival. © 2014 Korean Society of Hematology.
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