[新型药物时代原发性浆细胞白血病的预后因素分析]。

Q3 Medicine
J J Deng, X Y Jin, Z Y Zhang, H X Zhou, G Z Yang, C Y Geng, Y Jian, W M Chen, W Gao
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引用次数: 0

摘要

目的:探讨新型药物时代原发性浆细胞白血病(pPCL)的预后因素:探讨新型药物时代原发性浆细胞白血病(pPCL)的预后因素。方法回顾性收集首都医科大学附属北京朝阳医院血液科2011年至2022年收治的66例原发性浆细胞白血病患者的临床资料,分析其预后因素。结果66 名 pPCL 患者的中位年龄为 59 岁(29-79 岁)。中位总生存期(OS)为19.0(95% CI 10.4-27.6)个月,中位无进展生存期(PFS)为11.0(95% CI 6.5-15.6)个月。治疗后最佳反应为很好部分缓解(VGPR)或更好的患者的中位 OS 和 PFS 明显长于反应为部分缓解(PR)或更差的患者(中位 OS:33.0 个月 vs 6.0 个月):33.0 个月 vs 6.0 个月,Pvs 3.0 个月,Pvs 6.0 个月,P=0.002),接受移植的患者的 PFS 有比未接受移植的患者更长的趋势(19.0 个月 vs 8.0 个月,P=0.299)。接受维持治疗的患者的中位 OS 和 PFS 明显长于未接受维持治疗的患者(中位 OS:56.0 个月 vs 4.0 个月):而接受维持治疗(HR=0.075,95% CI 0.022-0.253,PHR=0.175,95% CI 0.048-0.638,P=0.008)是pPCL患者的独立保护因素。结论在使用新型药物的时代,高钙血症、接受维持治疗以及治疗后反应达到或优于VGPR是pPCL的独立预后因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Analysis of the prognostic factors in primary plasma cell leukemia in the era of novel agents].

Objective: To explore the prognostic factors of primary plasma cell leukemia (pPCL) in the era of novel agents. Methods: The clinical data of 66 patients with pPCL treated at the Department of Haematology, Beijing Chao-Yang Hospital, Capital Medical University from 2011 to 2022 were retrospectively collected to analyze their prognostic factors. Results: Among the 66 patients with pPCL, the median age was 59 (range: 29-79) years. The median overall survival (OS) duration was 19.0 (95% CI 10.4-27.6) months, and the median progression-free survival (PFS) duration was 11.0 (95% CI 6.5-15.6) months. The median OS and PFS were significantly longer in patients with the best post-treatment response of very good partial remission (VGPR) or better than in patients with a response of partial remission (PR) or worse (median OS: 33.0 months vs 6.0 months, P<0.001; median PFS: 16.0 months vs 3.0 months, P<0.001). OS was significantly longer in patients who underwent autologous hematopoietic stem cell transplantation than in those who did not undergo transplantation (49.0 months vs 6.0 months, P=0.002), and there was a trend toward a longer PFS in patients who underwent transplantation than in those who did not undergo transplantation (19.0 months vs 8.0 months, P=0.299). The median OS and PFS were significantly longer in patients who received maintenance therapy than in those who did not receive maintenance therapy (median OS: 56.0 months vs 4.0 months, P<0.001; median PFS: 20.0 months vs 2.0 months, P<0.001). Multivariate analysis showed that hypercalcemia was an independent risk factor (HR=3.204, 95% CI 1.068-9.610, P=0.038) for patients with pPCL, while receiving maintenance therapy (HR=0.075, 95% CI 0.022-0.253, P<0.001) and post-treatment response of VGPR or better (HR=0.175, 95% CI 0.048-0.638, P=0.008) were independent protective factors for patients with pPCL. Conclusions: In the era of novel agents, hypercalcemia, receiving maintenance therapy, and post-treatment response of VGPR or better are independent prognostic factors for pPCL.

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