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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

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dc.contributor.authorHwang, K.-L.-
dc.contributor.authorSong, M.-K.-
dc.contributor.authorShin, H.-J.-
dc.contributor.authorNa, H.-J.-
dc.contributor.authorShin, D.-H.-
dc.contributor.authorKim, J.-K.-
dc.contributor.authorMoon, J.-H.-
dc.contributor.authorAhn, J.-S.-
dc.contributor.authorSong, I.-C.-
dc.contributor.authorHong, J.-
dc.contributor.authorLee, G.-W.-
dc.contributor.authorChung, J.-S.-
dc.date.available2020-02-28T18:44:29Z-
dc.date.created2020-02-12-
dc.date.issued2014-
dc.identifier.issn2287-979X-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/12974-
dc.description.abstractBackground 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.-
dc.language영어-
dc.language.isoen-
dc.publisherKorean Society of Hematology-
dc.relation.isPartOfBlood Research-
dc.subjectazacitidine-
dc.subjecthydroxyurea-
dc.subjectadult-
dc.subjectaged-
dc.subjectArticle-
dc.subjectcancer chemotherapy-
dc.subjectcancer prognosis-
dc.subjectcancer survival-
dc.subjectcancer survivor-
dc.subjectchromosome 5-
dc.subjectchromosome 7-
dc.subjectchromosome aberration-
dc.subjectcomplex karyotype-
dc.subjectcontrolled study-
dc.subjectcytogenetics-
dc.subjectdrug dose reduction-
dc.subjectfemale-
dc.subjectfollow up-
dc.subjecthuman-
dc.subjectInternational Prognostic Scoring System-
dc.subjectkaryotype-
dc.subjectmajor clinical study-
dc.subjectmale-
dc.subjectmonosomal karyotype-
dc.subjectmyelodysplastic syndrome-
dc.subjectmyeloproliferative neoplasm-
dc.subjectoutcome assessment-
dc.subjectoverall survival-
dc.subjectretrospective study-
dc.subjectsex ratio-
dc.subjecttherapy delay-
dc.subjecttreatment duration-
dc.titleMonosomal and complex karyotypes as prognostic parameters in patients with International Prognostic Scoring System higher risk myelodysplastic syndrome treated with azacitidine-
dc.typeArticle-
dc.type.rimsART-
dc.description.journalClass1-
dc.identifier.doi10.5045/br.2014.49.4.234-
dc.identifier.bibliographicCitationBlood Research, v.49, no.4, pp.234 - 240-
dc.identifier.kciidART001937018-
dc.identifier.scopusid2-s2.0-84920995801-
dc.citation.endPage240-
dc.citation.startPage234-
dc.citation.titleBlood Research-
dc.citation.volume49-
dc.citation.number4-
dc.contributor.affiliatedAuthorHong, J.-
dc.type.docTypeArticle-
dc.subject.keywordAuthorAzacitidine-
dc.subject.keywordAuthorChromosomal abnormalities-
dc.subject.keywordAuthorComplex karyotype-
dc.subject.keywordAuthorMonosomal karyotype-
dc.subject.keywordAuthorMyelodysplastic syndrome-
dc.subject.keywordPlusazacitidine-
dc.subject.keywordPlushydroxyurea-
dc.subject.keywordPlusadult-
dc.subject.keywordPlusaged-
dc.subject.keywordPlusArticle-
dc.subject.keywordPluscancer chemotherapy-
dc.subject.keywordPluscancer prognosis-
dc.subject.keywordPluscancer survival-
dc.subject.keywordPluscancer survivor-
dc.subject.keywordPluschromosome 5-
dc.subject.keywordPluschromosome 7-
dc.subject.keywordPluschromosome aberration-
dc.subject.keywordPluscomplex karyotype-
dc.subject.keywordPluscontrolled study-
dc.subject.keywordPluscytogenetics-
dc.subject.keywordPlusdrug dose reduction-
dc.subject.keywordPlusfemale-
dc.subject.keywordPlusfollow up-
dc.subject.keywordPlushuman-
dc.subject.keywordPlusInternational Prognostic Scoring System-
dc.subject.keywordPluskaryotype-
dc.subject.keywordPlusmajor clinical study-
dc.subject.keywordPlusmale-
dc.subject.keywordPlusmonosomal karyotype-
dc.subject.keywordPlusmyelodysplastic syndrome-
dc.subject.keywordPlusmyeloproliferative neoplasm-
dc.subject.keywordPlusoutcome assessment-
dc.subject.keywordPlusoverall survival-
dc.subject.keywordPlusretrospective study-
dc.subject.keywordPlussex ratio-
dc.subject.keywordPlustherapy delay-
dc.subject.keywordPlustreatment duration-
dc.description.journalRegisteredClassscopus-
dc.description.journalRegisteredClasskci-
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