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Characteristics and clinical outcome of high-risk multiple myeloma patients in Korea (KMM 1805)
DC Field | Value | Language |
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dc.contributor.author | 김진석 | - |
dc.date.accessioned | 2023-06-02T00:43:57Z | - |
dc.date.available | 2023-06-02T00:43:57Z | - |
dc.date.issued | 2022-07 | - |
dc.identifier.issn | 0925-5710 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/194387 | - |
dc.description.abstract | Optimal treatments for multiple myeloma (MM) patients with high-risk cytogenetics must be determined, but subgroup features are not well-defined. We used real-world data from the Korean Myeloma Registry (KMR) to analyze the characteristics and clinical outcomes of newly diagnosed MM patients with ≥ 1 high-risk cytogenetic abnormality: Group 1: t(4;14) or t(14;16); Group 2: del(17p); Group 3: t(4;14)/del(17p) or t(14;16)/del(17p). Overall, 347 high-risk patients were identified (males, 48.7%; median age, 63 years). Median progression-free survival (PFS) and overall survival (OS) were 19.0 months (95% CI 17.0-20.0) and 50.0 months (95% CI 37.0-61.0), respectively. PFS (p = 0.047) and OS (p = 0.020) differed significantly between groups. After stratification by transplant eligibility, PFS and OS were significantly poorer in Group 3 among transplant-eligible patients, and even poorer in those with gain(1q). Patients stratified by cytogenetic abnormality and revised International Staging System (R-ISS) had significantly different PFS (p < 0.001) and OS (p = 0.003), with the worst survival in R-ISS III/Group 3 (median OS 21.0 months). Higher number of high-risk cytogenetic abnormalities was a negative prognostic marker for PFS and OS (p < 0.001). Real-world KMR data showed that risk factors for poor prognosis of MM patients included del(17p), R-ISS stage, and number of cytogenetic abnormalities. | - |
dc.description.statementOfResponsibility | restriction | - |
dc.language | English | - |
dc.publisher | Springer Japan | - |
dc.relation.isPartOf | INTERNATIONAL JOURNAL OF HEMATOLOGY | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.subject.MESH | Chromosome Aberrations | - |
dc.subject.MESH | Cytogenetic Analysis | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Middle Aged | - |
dc.subject.MESH | Multiple Myeloma* / diagnosis | - |
dc.subject.MESH | Multiple Myeloma* / genetics | - |
dc.subject.MESH | Multiple Myeloma* / therapy | - |
dc.subject.MESH | Prognosis | - |
dc.subject.MESH | Risk Factors | - |
dc.title | Characteristics and clinical outcome of high-risk multiple myeloma patients in Korea (KMM 1805) | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Internal Medicine (내과학교실) | - |
dc.contributor.googleauthor | Kihyun Kim | - |
dc.contributor.googleauthor | Jin Seok Kim | - |
dc.contributor.googleauthor | Sung-Soo Yoon | - |
dc.contributor.googleauthor | Dok Hyun Yoon | - |
dc.contributor.googleauthor | Hyeon-Seok Eom | - |
dc.contributor.googleauthor | Je-Jung Lee | - |
dc.contributor.googleauthor | Hyeon Woo Yim | - |
dc.contributor.googleauthor | Misun Park | - |
dc.contributor.googleauthor | Hojoon Lee | - |
dc.contributor.googleauthor | Chang-Ki Min | - |
dc.identifier.doi | 10.1007/s12185-022-03332-w | - |
dc.contributor.localId | A01017 | - |
dc.relation.journalcode | J01120 | - |
dc.identifier.eissn | 1865-3774 | - |
dc.identifier.pmid | 35543899 | - |
dc.identifier.url | https://link.springer.com/article/10.1007/s12185-022-03332-w | - |
dc.subject.keyword | High-risk cytogenetic abnormality | - |
dc.subject.keyword | Korean Myeloma Registry | - |
dc.subject.keyword | Multiple myeloma | - |
dc.subject.keyword | Survival | - |
dc.contributor.alternativeName | Kim, Jin Seok | - |
dc.contributor.affiliatedAuthor | 김진석 | - |
dc.citation.volume | 116 | - |
dc.citation.number | 1 | - |
dc.citation.startPage | 110 | - |
dc.citation.endPage | 121 | - |
dc.identifier.bibliographicCitation | INTERNATIONAL JOURNAL OF HEMATOLOGY, Vol.116(1) : 110-121, 2022-07 | - |
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