Cheng Ping, Guan Jun, Zhou Ying, Wang Qiu-Xiang, Wang Lan-Lan, Zhang Ting, Cheng Hui
Department of Hematology, The First Hospital of Wuhan, Wuhan 430022, Hubei Province, China.
Department of Hematology, The First Hospital of Wuhan, Wuhan 430022, Hubei Province, China .E-mail:
Zhongguo Shi Yan Xue Ye Xue Za Zhi. 2024 Feb;32(1):164-170. doi: 10.19746/j.cnki.issn.1009-2137.2024.01.026.
To investigate the value of immunoglobulin heavy chain () gene rearrangement in monitoring minimal residual disease (MRD) in multiple myeloma (MM) received autologous hematopoietic stem cell transplantation(auto-HSCT).
The clinical data of 26 MM patients who received auto-HSCT in the Department of Hematology, Wuhan First Hospital from 2018 to 2022 were collected. rearrangement was detected by multiplex PCR combined with capillary electrophoresis fragment analysis to evaluate minimal residual disease (MRD), and the outcome of the disease was analyzed statistically.
Among the 26 MM patients, 18 were males and 8 were females, with a median age of 59(41-70) years. The median follow-up time after transplantation was 33 (7-52) months. Compared with the rearrangement negative group (=17), the proportion of CR and sCR of patients with rearrangement positive in bone marrow samples before auto-HSCT at 3 months after transplantation was lower (1/9 14/17), and the duration of remission (DOR) after transplantation was shorter(10.78±4.35 15.88±5.22 months), with statistically significant difference in DOR between the two groups( < 0.05). Compared with rearrangement negative group (=21), the proportion of CR and sCR of patients with positive rearrangement results from peripheral blood stem cell collection at 3 months after transplantation was lower(0/5 15/21), the duration of remission (DOR) after transplantation was shorter(9.60±4.83 15.19±5.11 months), and the difference in DOR between the two groups was statistically significant ( < 0.05). During the follow-up period, 5 patients (5/9) with positive rearrangement results in bone marrow specimens died, and all patients with negative rearrangement results survived. Four patients (4/5) with positive rearrangement results by peripheral blood stem cell samples died, while one patient (1/21) with negative rearrangement results died. In both bone marrow and peripheral blood stem cell samples, the survival time of rearrangement-positive patients after transplantation was shorter than that of rearrangement-negative patients( < 0.05). Logistic regression analysis showed that gender, disease stage, the proportion of bone marrow smear plasma cells at initial diagnosis, stem cell mobilization plan, efficacy evaluation before transplantation (≥CR and <CR), and CD34 cell count had no effect on rearrangement results of stem cell collection ( >0.05).
By detecting rearrangement of MM patients receiving auto-HSCT, the depth of MRD can be further evaluated, which has a certain guiding significance for the efficacy and prognosis of the disease.
探讨免疫球蛋白重链()基因重排在监测接受自体造血干细胞移植(auto-HSCT)的多发性骨髓瘤(MM)微小残留病(MRD)中的价值。
收集2018年至2022年在武汉市第一医院血液科接受auto-HSCT的26例MM患者的临床资料。采用多重聚合酶链反应(PCR)结合毛细管电泳片段分析检测重排,以评估微小残留病(MRD),并对疾病转归进行统计学分析。
26例MM患者中,男性18例,女性8例,中位年龄59(41 - 70)岁。移植后中位随访时间为33(7 - 52)个月。与重排阴性组(=17)相比,auto-HSCT前骨髓样本重排阳性的患者在移植后3个月时完全缓解(CR)和严格完全缓解(sCR)的比例较低(1/9 14/17),移植后缓解持续时间(DOR)较短(10.78±4.35 15.88±5.22个月),两组DOR差异有统计学意义(<0.05)。与重排阴性组(=21)相比,移植后3个月外周血干细胞采集时重排结果阳性的患者CR和sCR的比例较低(0/5 15/21),移植后缓解持续时间(DOR)较短(9.60±4.83 15.19±5.11个月),两组DOR差异有统计学意义(<0.05)。随访期间,骨髓标本重排结果阳性的5例患者(5/9)死亡,重排结果阴性的患者均存活。外周血干细胞样本重排结果阳性的4例患者(4/5)死亡,重排结果阴性的1例患者(1/21)死亡。在骨髓和外周血干细胞样本中,重排阳性患者移植后的生存时间均短于重排阴性患者(<0.05)。Logistic回归分析显示,性别、疾病分期、初诊时骨髓涂片浆细胞比例、干细胞动员方案以及移植前疗效评估(≥CR和<CR)和CD34细胞计数对干细胞采集时的重排结果均无影响(>0.05)。
通过检测接受auto-HSCT的MM患者的重排,可进一步评估MRD深度这对疾病的疗效和预后具有一定的指导意义。