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

被引:1
作者
Kim, Kihyun [1 ]
Kim, Jin Seok [2 ]
Yoon, Sung-Soo [3 ]
Yoon, Dok Hyun [4 ]
Eom, Hyeon-Seok [5 ]
Lee, Je-Jung [6 ]
Yim, Hyeon Woo [7 ,8 ]
Park, Misun [8 ]
Lee, Hojoon [9 ]
Min, Chang-Ki [10 ]
机构
[1] Sungkyunkwan Univ, Samsung Med Ctr, Sch Med, Div Hematol Oncol,Dept Med, Seoul, South Korea
[2] Yonsei Univ, Coll Med, Severance Hosp, Div Hematol,Dept Internal Med, Seoul, South Korea
[3] Seoul Natl Univ, Seoul Natl Univ Hosp, Dept Internal Med, Div Hematol Oncol,Coll Med, Seoul, South Korea
[4] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Oncol, Seoul, South Korea
[5] Natl Canc Ctr, Ctr Hematol Malignancy, Dept Hematol Oncol, Goyang Si, Gyunggi Do, South Korea
[6] Chonnam Natl Univ, Hwasun Hosp, Med Sch, Dept Hematol Oncol, Hwasun, Jeollanm Do, South Korea
[7] Catholic Univ Korea, Coll Med, Dept Prevent Med, Seoul, South Korea
[8] Catholic Univ Korea, Coll Med, Clin Res Coordinating Ctr, Seoul, South Korea
[9] Amgen Korea, Seoul, South Korea
[10] Catholic Univ Korea, Seoul St Marys Hosp, Dept Hematol, Coll Med, Seoul, South Korea
关键词
High-risk cytogenetic abnormality; Korean Myeloma Registry; Multiple myeloma; Survival; INTERNATIONAL STAGING SYSTEM; STEM-CELL TRANSPLANTATION; CYTOGENETIC ABNORMALITIES; INDUCTION THERAPY; BORTEZOMIB; CHROMOSOME-13; DEXAMETHASONE; PATHOGENESIS; PROGRESSION; IMPACT;
D O I
10.1007/s12185-022-03332-w
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:110 / 121
页数:12
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