1.陆军军医大学第二附属医院血液病医学中心,重庆 400037
2.陆军军医大学第二附属医院金凤实验室,重庆 401329
Received:17 February 2025,
Revised:2025-07-01,
Accepted:15 July 2025,
Published:28 October 2025
移动端阅览
刘嘉,朱丽丹,高世春,等.贝林妥欧单抗桥接异基因造血干细胞移植治疗微小残留病阳性急性B淋巴细胞白血病疗效分析[J].重庆医科大学学报,2025,50(10):1453-1456.
Liu Jia,Zhu Lidan,Gao Shichun,et al.Efficacy of blinatumomab as a bridge therapy for allogeneic hematopoietic stem cell transplantation in treatment of minimal residual disease-positive B-lineage acute lymphoblastic leukemia[J].Journal of Chongqing Medical University,2025,50(10):1453-1456.
刘嘉,朱丽丹,高世春,等.贝林妥欧单抗桥接异基因造血干细胞移植治疗微小残留病阳性急性B淋巴细胞白血病疗效分析[J].重庆医科大学学报,2025,50(10):1453-1456. DOI: 10.13406/j.cnki.cyxb.003939.
Liu Jia,Zhu Lidan,Gao Shichun,et al.Efficacy of blinatumomab as a bridge therapy for allogeneic hematopoietic stem cell transplantation in treatment of minimal residual disease-positive B-lineage acute lymphoblastic leukemia[J].Journal of Chongqing Medical University,2025,50(10):1453-1456. DOI: 10.13406/j.cnki.cyxb.003939.
目的
2
探索有效治疗策略,以降低异基因造血干细胞移植(allogeneic hematopoietic stem cell transplantation,allo-HSCT)前微小残留病(minimal residual disease,MRD)阳性急性B淋巴细胞白血病(acute B-cell lymphocyte leukemia,B-ALL)患者移植后高复发风险。
方法
2
回顾性分析陆军军医大学第二附属医院血液病医学中心2022年11月至2024年11月10例移植前MRD阳性B-ALL患者,中位年龄30(7~56)岁,男4例,女6例,4例无关供者移植,6例亲缘间单倍体移植。10例患者均给予贝林妥欧单抗(≥45 kg,28 µg/d,14 d;
<
45 kg,5 µg/m
2
/d,14 d),7 d之内桥接异基因造血干细胞移植预处理。
结果
2
10例患者经贝林妥欧单抗治疗后MRD均转阴,造血干细胞移植后100%供者造血重建,中性粒细胞重建中位时间12(9~22)d,血小板重建中位时间13.5(9~22)d。至2025年1月,中位观察时间14(2~26)个月,2例复发,1例MRD转阳,复发率20%;9例存活,1例死于疾病复发,1例复发后经Car T细胞治疗再次达到完全缓解,MRD转阳患者经白细胞介素-2(interleukin-2,IL-2)治疗MRD再次转阴,目前均存活。治疗期间,有1例患者并发细胞因子释放综合征,1例患者并发新冠病毒感染,1例患者并发带状疱疹及病毒性脑炎,3例患者出现Ⅰ~Ⅱ度急性移植物抗宿主病,4例出现慢性移植物抗宿主病,无移植相关微血栓病变发生。
结论
2
贝林妥欧单抗桥接异基因造血干细胞移植治疗MRD阳性B-ALL可明显降低移植后复发、并发症较少且易控制,后续可通过多中心、随机对照临床研究进一步验证其有效性和安全性。
Objective
2
To investigate effective strategies to reduce the high risk of recurrence after allogeneic hematopoietic stem cell transplantation(allo-HSCT) in patients with minimal residual disease(MRD)-positive B-lineage acute lymphoblastic leukemia(B-ALL).
Methods
2
A retrospective analysis was performed for ten B-ALL patients with positive MRD before transplantation at our center from November 2022 to November 2024. There were four male patients and six female patients,with a median age of 30(7-56) years. Of all patients,four received transplantation from unrelated donors,and six received haploidentical transplantation from relatives. All ten patients received blinatumomab(28 µg/day for 14 days for patients ≥45 kg; 5 µg/m²/day for 14 days for patients <45 kg) and were bridged to the conditioning regimen for allo-HSCT within 7 days.
Results
2
After treatment with blinatumomab,all ten patients achieved the clearance of MRD. After allo-HSCT,100% of the patients achieved donor hematopoietic reconstitution. The median time to neutrophil reconstitution was 12(9-22) days,and the median time to platelet reconstitution was 13.5(9-22) days. As of January 2025,the median observation time was 14(2-26) months; of all patients,two experienced recurrence,and one had positive MRD again,with a recurrence rate of 20%. Among the ten patients,nine survived and one died of disease recurrence. One patient achieved complete remission again after chimeric antigen receptor T-cell(CAR-T) therapy following recurrence,and the patient with positive MRD achieved the clearance of MRD again after interleukin-2 treatment; both patients were currently alive. During treatment,one patient developed cytokine release syndrome,one patient was comorbid with SARS-CoV-2 infection,one patient had herpes zoster and viral encephalitis,three patients developed grade Ⅰ-Ⅱ acute graft-versus-host disease,and four patients developed chronic graft-versus-host disease; no transplantation-associated thrombotic microangiopathy was observed.
Conclusion
2
For patients with MRD-positive B-ALL,blinatumomab as a bridge therapy for allo-HSCT can significantly reduce recurrence after transplantation,with fewer complications that are easy to control. Multicenter randomized controlled clinical studies can be performed to further verify its efficacy and safety.
中国抗癌协会血液肿瘤专委会 , 中华医学会血液学分会白血病淋巴瘤学组 . 中国成人急性淋巴细胞白血病诊断与治疗指南(2024) [J ] . 中华血液学杂志 , 2024 , 45 ( 5 ): 417 - 429 .
Hematology Oncology Committee , Chinese Anti-Cancer Association , Leukemia & Lymphoma Group , Chinese Society of Hematology , Chinese Medical Association . Chinese guideline for diagnosis and treatment of adult acute lymphoblastic leukemia(2024) [J ] . Chin J Hematol , 2024 , 45 ( 5 ): 417 - 429 .
中国临床肿瘤学会指南工作委员会 . 儿童及青少年白血病诊疗指南2022 [M ] . 北京 : 人民卫生出版社 , 2022 .
Chinese Society of Clinical Oncology . Clinical guideline for diagnosis and treatment of leukemias in children and adolescent(2022) [M ] . Beijing : People’s Health Publishing House , 2022 .
沈雨晴 , 莫 霖 , 余 璐 , 等 . 急性白血病患儿行为特征的潜在类别分析及影响因素 [J ] . 重庆医科大学学报 , 2024 , 49 ( 3 ): 303 - 310 .
Shen YQ , Mo L , Yu L , et al . Latent class analysis of behavioral characteristics of children with acute leukemia and associated influencing factors [J ] . J Chongqing Med Univ , 2024 , 49 ( 3 ): 303 - 310 .
Gökbuget N , Boissel N , Chiaretti S , et al . Diagnosis,prognostic factors,and assessment of ALL in adults: 2024 ELN recommendations from a European expert panel [J ] . Blood , 2024 , 143 ( 19 ): 1891 - 1902 .
张瑞东 , 王天友 . 儿童急性淋巴细胞白血病的免疫治疗 [J ] . 中华儿科杂志 , 2023 , 61 ( 10 ): 865 - 868 .
Zhang RD , Wang TY . Immunotherapy in pediatric acute lymphoblastic leukemia [J ] . Chin J Pediatr , 2023 , 61 ( 10 ): 865 - 868 .
Ye XS , Wu YQ , Zhang HQ , et al . Rapid generation of CD19 CAR-T cells by minicircle DNA enables anti-tumor activity and prevents fatal CAR-B leukemia [J ] . Cancer Lett , 2023 , 568 : 216278 .
von Stackelberg A , Locatelli F , Zugmaier G , et al . Phase Ⅰ/phase Ⅱ study of blinatumomab in pediatric patients with relapsed/refractory acute lymphoblastic leukemia [J ] . J Clin Oncol , 2016 , 34 ( 36 ): 4381 - 4389 .
Gökbuget N , Dombret H , Bonifacio M , et al . Blinatumomab for minimal residual disease in adults with B-cell precursor acute lymphoblastic leukemia [J ] . Blood , 2018 , 131 ( 14 ): 1522 - 1531 .
Kantarjian H , Stein A , Gökbuget N , et al . Blinatumomab versus chemotherapy for advanced acute lymphoblastic leukemia [J ] . N Engl J Med , 2017 , 376 ( 9 ): 836 - 847 .
Wang Y , Chang YJ , Chen J , et al . Consensus on the monitoring,treatment,and prevention of leukaemia relapse after allogeneic haematopoietic stem cell transplantation in China:2024 update [J ] . Cancer Lett , 2024 , 605 : 217264 .
Gökbuget N , Kneba M , Raff T , et al . Adult patients with acute lymphoblastic leukemia and molecular failure display a poor prognosis and are candidates for stem cell transplantation and targeted therapies [J ] . Blood , 2012 , 120 ( 9 ): 1868 - 1876 .
Bassan R , Spinelli O , Oldani E , et al . Improved risk classification for risk-specific therapy based on the molecular study of minimal residual disease(MRD) in adult acute lymphoblastic leukemia(ALL) [J ] . Blood , 2009 , 113 ( 18 ): 4153 - 4162 .
Zhou Y , Slack R , Jorgensen JL , et al . The effect of peritransplant minimal residual disease in adults with acute lymphoblastic leukemia undergoing allogeneic hematopoietic stem cell transplantation [J ] . Clin Lymphoma Myeloma Leuk , 2014 , 14 ( 4 ): 319 - 326 .
Bassan R , Spinelli O , Oldani E , et al . Different molecular levels of post-induction minimal residual disease may predict hematopoietic stem cell transplantation outcome in adult Philadelphia-negative acute lymphoblastic leukemia [J ] . Blood Cancer J , 2014 , 4 ( 7 ): e225 .
Bader P , Salzmann-Manrique E , Balduzzi A , et al . More precisely defining risk peri-HCT in pediatric ALL:pre- vs post-MRD measures,serial positivity,and risk modeling [J ] . Blood Adv , 2019 , 3 ( 21 ): 3393 - 3405 .
Lyons KU , Gore L . Bispecific T-cell engagers in childhood B-acute lymphoblastic leukemia [J ] . Haematologica , 2024 , 109 ( 6 ): 1668 - 1676 .
0
Views
3
下载量
0
CSCD
Publicity Resources
Related Articles
Related Author
Related Institution
京公网安备11010802024621
