19例新治多发性骨髓瘤患者t(14;16)]。

Y Li, J R Liu, J Li, W M Chen
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引用次数: 0

摘要

目的:探讨t(14;16)异常的新诊断多发性骨髓瘤(MM)患者的预后。方法:收集2018年1月至2020年11月首都医科大学附属北京朝阳医院和中山大学第一附属医院564例首发MM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FISH正常患者的预后以及t(4;14)和del (17p)患者的预后进行比较。结果:564例新诊断MM患者中,出现t(14;16)异常19例(3.4%),其中1q21+ 14例,del 3例(17p)。与正常FISH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vs未达到,Pvs未达到,P=0.002)。倾向评分匹配后,15例t(14;16)组患者与15例t(4;14)组患者的PFS和OS无统计学差异(中位PFS: 13.0个月vs未达到,P=0.247;中位OS: 42个月vs未达到,P=0.609)。同样,15例t组患者(14;16)和15例del组患者(17p)的PFS和OS无统计学差异(中位PFS: 13个月vs 31个月,P=0.939;中位OS: 42个月vs 37.3个月,P=0.557)。倾向评分匹配显示,当联合1q21+时,t患者(14;16)与t患者(4;14)或del患者(17p)的PFS和OS差异无统计学意义(均P < 0.05)。t(14;16)患者是否进行了自体造血干细胞移植对PFS和OS无显著影响(P < 0.05)。结论:在新诊断的MM患者中,t(14;16)常与高危细胞遗传学异常相关,其不良预后价值与t(4;14)和del (17p)相似。
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[Prognostic analysis of 19 newly treated multiple myeloma patients with t(14; 16)].

Objective: To investigate the prognosis of newly diagnosed multiple myeloma (MM) patients with t (14;16) abnormality. Methods: 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) . Results: 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 vs not reached, P<0.001; the median OS: 42 months vs not reached, P=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 vs not reached, P=0.247; the median OS: 42 months vs not reached, P=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 vs 31 months, P=0.939; the median OS: 42 months vs 37.3 months, P=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 P>0.05). Whether or not the patients with t (14;16) had undergone auto-HSCT did not significantly impact the PFS and OS (all P>0.05) . Conclusion: 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) .

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