Wu Yong-Li, Wang Nan, Yan Ying-Zhao, Yuan Li-Jun, Wang Li-Li, Li Hong-Hua, Li Meng
Department of Hematology, The First Medical Center, Chinese PLA General Hospital, Beijing 100853, China.
Department of Hematology, The First Medical Center, Chinese PLA General Hospital, Beijing 100853, China,E-mail:
Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2020 Dec;28(6):1804-1810. doi: 10.19746/j.cnki.issn.1009-2137.2020.06.003.
To evaluate the clinical characteristics, genetic abnormalities, treatment efficacy and prognostic factors in patients with plasma cell leukemia(PCL).
30 patients diagnosed as PCL in our hospital from January 1993 to December 2019 were enrolled, and the clinical characteristics, laboratory findings, therapeutic regimes, and survival data of the patients were retrospectively analyzed.
The median age of the 30 patients was 56.5 (28-80) years old, among them, 25 patients were primary plasma cell leukemia, and 5 patients were secondary plasma cell leukemia. Complex karyotypes and subdiploids were most common in cytogenetic abnormalities. Among the 20 cases of chromosome G banding, 11 (55%) cases were complex karyotypes and 8 (40%) cases were hypodiploid. Fluorescent in situ hybridization (FISH) test showed that among 11 cases, 6 cases showed 17p13 deletion, 8 cases showed at least two kinds of abnormalities, which including t (14; 16), t (8; 14), t (11;14), 17p13 deletion, and 13q14 deletion. The median overall survival (OS) time was 10.5 months for all patients. The median OS time of the patients in ECOG score ≤ 2 group was 21.5 months, which was significantly longer than those in the ECOG score>2 group(1.2 months) (P=0.017). The median OS time of the patients treated with novel agents (including proteasome inhibitor and/or immunomodulator) was 24.9 months, which was significantly longer than the patients treated with traditional chemotherapy group(10.5 months) (P<0.001). For the patients treated with novel agents, the median OS time of patients accepted two novel agents combination was 30.9 months, which was longer than those of single novel agent(11.5 months) (P=0.021). The effect of genetic abnormolity to the OS of the patients showed no statistical difference. Multivariate statistical analysis showed that ECOG score>2 was the independent prognostic factor of plasma cell leukemia patients. There were two patients underwent allogeneic hematopoietic stem cell transplantation in the study,but died due to the pulmonary infection within 6 months after transplantation.
In the era of novel agents, ECOG score is an independent prognostic factor of plasma cell leukemia. Multiple novel agents treatment should be underwent as soon as possible to improve the prognosis of the patients. Pulmonary infection is a common factor that cause the death of the patients after allogeneic hematopoietic stem cell transplantation.
评估浆细胞白血病(PCL)患者的临床特征、基因异常、治疗疗效及预后因素。
选取1993年1月至2019年12月在我院确诊为PCL的30例患者,回顾性分析患者的临床特征、实验室检查结果、治疗方案及生存数据。
30例患者的中位年龄为56.5(28 - 80)岁,其中原发性浆细胞白血病25例,继发性浆细胞白血病5例。细胞遗传学异常中复杂核型和亚二倍体最为常见。在20例染色体G显带分析中,11例(55%)为复杂核型,8例(40%)为亚二倍体。荧光原位杂交(FISH)检测显示,11例中6例存在17p13缺失,8例至少存在两种异常,包括t(14;16)、t(8;14)、t(11;14)、17p13缺失和13q14缺失。所有患者的中位总生存(OS)时间为10.5个月。ECOG评分≤2组患者的中位OS时间为21.5个月,显著长于ECOG评分>2组患者(1.2个月)(P = 0.017)。接受新型药物(包括蛋白酶体抑制剂和/或免疫调节剂)治疗的患者中位OS时间为24.9个月,显著长于接受传统化疗组患者(10.5个月)(P<0.001)。对于接受新型药物治疗的患者,接受两种新型药物联合治疗的患者中位OS时间为30.9个月,长于接受单一新型药物治疗的患者(11.5个月)(P = 0.021)。基因异常对患者OS的影响无统计学差异。多因素统计分析显示,ECOG评分>2是浆细胞白血病患者的独立预后因素。本研究中有2例患者接受了异基因造血干细胞移植,但均在移植后6个月内因肺部感染死亡。
在新型药物时代,ECOG评分是浆细胞白血病的独立预后因素。应尽早采用多种新型药物治疗以改善患者预后。肺部感染是异基因造血干细胞移植后患者死亡的常见因素。