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KMID : 0366220140490040234
Korean Journal of Hematology
2014 Volume.49 No. 4 p.234 ~ p.240
Monosomal and complex karyotypes as prognostic parameters in patients with International Prognostic Scoring System higher risk myelodysplastic syndrome treated with azacitidine
Hwang Kyung-Lim

Song Moo-Kon
Shin Ho-Jin
Na Hae-Jung
Shin Dong-Hun
Kim Joong-Keun
Moon Joon-Ho
Ahn Jae-Sook
Song Ik-Chan
Hong Jun-Shik
Lee Gyeong-Won
Chung Joo-Seop
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 clin-ical 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 treated with 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 mon-osomies 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 patients and MK was present in 90 patients. Bone marrow blasts ¡Ã15% and CK were associated with poorer response (P=0.038, P=0.007) and overall survival (OS) (P£¼0.001, P£¼0.001) 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 £¾3 CAs was associated with poorer OS (group including £¼3 CAs vs. only three CAs, P=0.001; group with £¾3 CAs vs. only three CAs, P=0.001).

Conclusion: CK was an important prognostic parameter associated with worse outcome. MK may pre-dict poor survival in only non-CK status. The higher number of CAs was associated with poorer survival.
KEYWORD
Myelodysplastic syndrome, Azacitidine, Complex karyotype, Monosomal karyotype, Chromosomal abnormalities
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