Suppr超能文献

韩国高危多发性骨髓瘤患者的特征和临床结局(KMM 1805)。

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

机构信息

Division of Hematology-Oncology, Department of Medicine, Sungkyunkwan University School of Medicine, Samsung Medical Center, Seoul, Korea.

Division of Hematology, Department of Internal Medicine, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.

出版信息

Int J Hematol. 2022 Jul;116(1):110-121. doi: 10.1007/s12185-022-03332-w. Epub 2022 May 11.

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.

摘要

多发性骨髓瘤(MM)高危细胞遗传学患者的最佳治疗方法必须确定,但亚组特征尚未明确。我们使用韩国骨髓瘤登记处(KMR)的真实数据,分析了新诊断的 MM 患者中≥1 种高危细胞遗传学异常的特征和临床结局:第 1 组:t(4;14)或 t(14;16);第 2 组:del(17p);第 3 组:t(4;14)/del(17p)或 t(14;16)/del(17p)。共有 347 例高危患者被确定(男性占 48.7%;中位年龄为 63 岁)。中位无进展生存期(PFS)和总生存期(OS)分别为 19.0 个月(95%CI 17.0-20.0)和 50.0 个月(95%CI 37.0-61.0)。PFS(p=0.047)和 OS(p=0.020)在各组间差异有统计学意义。在根据移植资格分层后,在可移植患者中,第 3 组的 PFS 和 OS 差异具有统计学意义,而在那些具有增益(1q)的患者中则更差。根据细胞遗传学异常和修订的国际分期系统(R-ISS)分层的患者,PFS(p<0.001)和 OS(p=0.003)差异有统计学意义,在 R-ISS III/第 3 组中生存最差(中位 OS 21.0 个月)。高危细胞遗传学异常的数量是 PFS 和 OS 的不良预后标志物(p<0.001)。真实世界 KMR 数据显示,影响 MM 患者预后不良的危险因素包括 del(17p)、R-ISS 分期和细胞遗传学异常数量。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验