Li Y, Liu J R, Li J, Chen W M
Department of Hematology, Beijing Chaoyang Hospital, Capital Medical University, Myeloma Research Center of Beijing, Beijing 100020, China Peking University People's Hospital, Peking University Institute of Hematology, National Clinical Research Center for Hematologic Disease, Beijing Key Laboratory of Hematopoietic Stem Cell Transplantation for Hematological Diseases, Beijing 100044, China.
Department of Hematology, The First Affiliated Hospital of Sun Yat-Sen University, Guangzhou 510080, China.
Zhonghua Xue Ye Xue Za Zhi. 2024 Oct 14;45(10):944-950. doi: 10.3760/cma.j.cn121090-20240814-00303.
To investigate the prognosis of newly diagnosed multiple myeloma (MM) patients with t (14;16) abnormality. Clinical data from 564 patients diagnosed with initial MM from January 2018 to November 2020 at Beijing Chaoyang Hospital affiliated with Capital Medical University and the First Affiliated Hospital of Sun Yat-sen University were collected and retrospectively analyzed. The prognoses of patients with t (14;16) were analyzed and compared with the prognoses of patients with normal FISH, and those with t (4;14) and del (17p) . Among 564 newly diagnosed MM patients, 19 (3.4%) exhibited t (14;16) abnormalities, with 14 cases diagnosed with 1q21+ and three cases with del (17p). Progression-free survival (PFS) and overall survival (OS) of patients with t (14;16) were significantly shorter compared with patients with normal FISH (the median PFS: 14 months not reached, <0.001; the median OS: 42 months not reached, =0.002). No statistically significant difference was detected in PFS and OS between the 15 patients with t (14;16) and the 15 with t (4;14) after propensity score matching (the median PFS: 13.0 months not reached, =0.247; the median OS: 42 months not reached, =0.609). Similarly, no statistically significant difference was observed in PFS and OS between 15 patients with t (14;16) and 15 with del (17p) (the median PFS: 13 months 31 months, =0.939; the median OS: 42 months 37.3 months, =0.557). Propensity score matching indicated that when combined with 1q21+, no statistically significant differences were present in PFS and OS between patients with t (14;16) and patients with t (4;14) or patients with del (17p) (all >0.05). Whether or not the patients with t (14;16) had undergone auto-HSCT did not significantly impact the PFS and OS (all >0.05) . t (14;16) is often associated with high-risk cytogenetic abnormalities in newly diagnosed MM patients, and its adverse prognostic value is similar to that of t (4;14) and del (17p) .
探讨新诊断的伴有t(14;16)异常的多发性骨髓瘤(MM)患者的预后。收集2018年1月至2020年11月在首都医科大学附属北京朝阳医院和中山大学附属第一医院初次诊断为MM的564例患者的临床资料并进行回顾性分析。分析t(14;16)患者的预后,并与荧光原位杂交(FISH)正常、t(4;14)和17p缺失患者的预后进行比较。在564例新诊断的MM患者中,19例(3.4%)表现出t(14;16)异常,其中14例诊断为1q21+,3例诊断为17p缺失。与FISH正常的患者相比,t(14;16)患者的无进展生存期(PFS)和总生存期(OS)显著缩短(中位PFS:14个月 未达到,<0.001;中位OS:42个月 未达到,=0.002)。倾向评分匹配后,15例t(14;16)患者和15例t(4;14)患者的PFS和OS未检测到统计学显著差异(中位PFS:13.0个月 未达到,=0.247;中位OS:42个月 未达到,=0.609)。同样,15例t(14;16)患者和15例17p缺失患者的PFS和OS也未观察到统计学显著差异(中位PFS:13个月 31个月,=0.939;中位OS:42个月 37.个月,=0.557)。倾向评分匹配表明,当与1q21+合并时,t(14;16)患者与t(4;14)患者或17p缺失患者的PFS和OS均无统计学显著差异(均>0.05)。t(14;16)患者是否接受自体造血干细胞移植(auto-HSCT)对PFS和OS均无显著影响(均>0.05)。t(14;16)常与新诊断的MM患者的高危细胞遗传学异常相关,其不良预后价值与t(4;14)和17p缺失相似。