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Characteristics and clinical outcome of high-risk multiple myeloma patients in Korea (KMM 1805) : x

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Authors

Kim, Kihyun; Kim, Jin Seok; Yoon, Sung-Soo; Yoon, Dok Hyun; Eom, Hyeon-Seok; Lee, Je-Jung; Yim, Hyeon Woo; Park, Misun; Lee, Hojoon; Min, Chang-Ki

Issue Date
2022-07
Publisher
Japanese Society of Hematology
Citation
International Journal of Hematology, Vol.116 No.1, pp.110-121
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.
ISSN
0925-5710
URI
https://hdl.handle.net/10371/184621
DOI
https://doi.org/10.1007/s12185-022-03332-w
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