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Comparison of 3-month cytogenetic and molecular assays for early assessment of long-term clinical impact after BCR-ABL1 tyrosine kinase inhibitor treatment in chronic myeloid leukemia

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dc.contributor.authorKee, Kyung-Mi-
dc.contributor.authorKim, Soo-Hyun-
dc.contributor.authorYang, Seon-Young-
dc.contributor.authorShin, Jeong-U-
dc.contributor.authorNam, Yoon-Won-
dc.contributor.authorJang, Eun-Jung-
dc.contributor.authorHong-Tae Kim-
dc.contributor.authorLee, Se-Min-
dc.contributor.authorPark, Sung-Ho-
dc.contributor.authorKim, Dong-Wook-
dc.date.accessioned2023-01-27T06:29:31Z-
dc.date.available2023-01-27T06:29:31Z-
dc.date.created2021-12-28-
dc.date.issued2022-01-
dc.identifier.issn0145-2126-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/12970-
dc.description.abstract© 2021 Elsevier LtdTo compare the clinical significance of 3-month cytogenetic and molecular monitoring, we analyzed 1,410 paired cytogenetic and molecular data from 705 chronic-phase chronic myeloid leukemia patients. Based on early cytogenetic response (ECyR, Ph+≤35 %) and molecular response (EMR, BCR-ABL1IS≤10 %) at 3 months, the patients were divided into four groups (group 1: ECyR + EMR, n = 560; group 2: no ECyR + EMR, n = 27; group 3: ECyR + no EMR, n = 55; group 4: no ECyR + no EMR, n = 63). By 10 years, major molecular response (MMR), deep molecular response (MR4.5), overall survival (OS), and progression-free survival (PFS) rates were significantly high in group 1 (P < 0.001). Comparing groups 2 and 3, the MMR (P = 0.096), MR4.5 (P = 0.945), OS (P = 0.832), and PFS (P = 0.627) rates tended to be higher in group 2, although not significantly. Thus, the cytogenetic assay can not only be useful but its addition may also provide a more precise prediction of MR4.5.-
dc.language영어-
dc.publisherPergamon Press Ltd.-
dc.titleComparison of 3-month cytogenetic and molecular assays for early assessment of long-term clinical impact after BCR-ABL1 tyrosine kinase inhibitor treatment in chronic myeloid leukemia-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000800672300003-
dc.identifier.scopusid2-s2.0-85121236079-
dc.identifier.rimsid76994-
dc.contributor.affiliatedAuthorHong-Tae Kim-
dc.identifier.doi10.1016/j.leukres.2021.106754-
dc.identifier.bibliographicCitationLeukemia Research, v.112-
dc.relation.isPartOfLeukemia Research-
dc.citation.titleLeukemia Research-
dc.citation.volume112-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaOncology-
dc.relation.journalResearchAreaHematology-
dc.relation.journalWebOfScienceCategoryOncology-
dc.relation.journalWebOfScienceCategoryHematology-
dc.subject.keywordPlusPOLYMERASE-CHAIN-REACTION-
dc.subject.keywordPlusBCR-ABL-
dc.subject.keywordPlusTRANSCRIPT LEVELS-
dc.subject.keywordPlusIMATINIB MESYLATE-
dc.subject.keywordPlusPHASE-
dc.subject.keywordPlusINTERFERON-
dc.subject.keywordPlusPREDICTS-
dc.subject.keywordPlusDASATINIB-
dc.subject.keywordPlusCML-
dc.subject.keywordPlusACHIEVEMENT-
dc.subject.keywordAuthorChronic myeloid leukemia-
dc.subject.keywordAuthorCytogenetic response-
dc.subject.keywordAuthorEarly response-
dc.subject.keywordAuthorMolecular response-
dc.subject.keywordAuthorTyrosine kinase inhibitor-
Appears in Collections:
Center for Genomic Integrity(유전체 항상성 연구단) > 1. Journal Papers (저널논문)
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