摘要
目的:探讨供者淋巴细胞输注(donor lymphocyte infusion,DLI)治疗异基因造血干细胞移植(allo-HSCT)后复发的高危白血病患者的疗效。方法:回顾性分析2000年8月至2015年4月期间在南方医科大学珠江医院行allo-HSCT后复发而予以供者淋巴细胞输注的15例高危白血病患者,以及期间行allo-HSCT后复发而未予以供者淋巴细胞输注的13例高危白血病患者,并对两类患者的1和3年OS率进行对比。结果:行DLI的15例患者的1和3年生存率分别为58.3%和46.7%,1和3年DFS率分别为22.0%和11.0%,患者的死亡原因主要为疾病复发(5例),急性GVHD反应(1例)。未行DLI术的13例患者1年和3年OS率分别为29.9%和15.0%,1年DFS率为11.2%,患者的死亡原因主要为疾病复发(9例)。移植后复发行DLI治疗的患者与未行DLI的患者相比,移植后复发行DLI治疗的患者的1和3年OS率均高于未行DLI患者,但两者OS率差异无统计学显著性(P=0.069)。结论:DLI治疗仍然是目前治疗移植后复发的较为有效的方法,联合其他方式或改变供者淋巴细胞的细胞输注类型或将可以提高DLI的疗效。
Objective:To investigate the efficacy of donor lymphocyte infusion(DLI) for treating relapsed high-risk leukemia patients after allogeneic hematopoietic stem cell transplantation(allo-HSCT).Methods:The data of 15 leukemia patients who had received DLI and 13 leukemia patients who had not received DLI in Zhujiang Hospital from2000 to 2014 were studied retrospectively,and their 1 and 3 year overall survival rate(OS) were compared between the two groups.Results:In 15 patients received DLI,the 1 and 3 year OS were 58.3%and 46.7%,the 1 and 3 year disease-free survival(DFS) were 22.0%and 11.0%,respectively.The main death cause in these patients included relapse(n = 5) and acute GVHD(n = 1),whereas in 13 patients who had not received DLI,the 1 and 3 year OS were29.9%and 15.0%respectively,their 1 year DFS were 11.2%.The main death cause in these patients were relapse(n= 9).The 1 and 3 year OS of patients who had received DLI was higher as compared with the patients who had not received DLI.but this difference was no statistically significant(P = 0.069).Conclusion:DLI is an effective method for treating patients with relapsed leukemia,and may improve the therapeutic efficacy of DLI by combining other methods or alternating the types of the donor lymphocytes.
出处
《中国实验血液学杂志》
CAS
CSCD
北大核心
2015年第4期982-988,共7页
Journal of Experimental Hematology
基金
国家自然科学基金面上项目(81372249)
国家自然科学基金青年项目(81300431)
广东省产学研项目(2013B091500072)
关键词
白血病
供者淋巴细胞输注
异基因造血干细胞移植
donor lymphocyte transfusion
leukemia
allogeneic hematopoietic stem cell transplantation