Optimized therapeutic strategy for patients with refractory or relapsed acute myeloid leukemia: long-term clinical outcomes and health-related quality of life assessment

被引:12
|
作者
Yan, Chen-hua [1 ,2 ,3 ]
Wang, Yu [1 ,2 ,3 ]
Sun, Yu-qian [1 ,2 ,3 ]
Cheng, Yi-fei [1 ,2 ,3 ]
Mo, Xiao-dong [1 ,2 ,3 ]
Wang, Feng-rong [1 ,2 ,3 ]
Chen, Yu-hong [1 ,2 ,3 ]
Zhang, Yuan-yuan [1 ,2 ,3 ]
Han, Ting-ting [1 ,2 ,3 ]
Chen, Huan [1 ,2 ,3 ]
Xu, Lan-ping [1 ,2 ,3 ]
Zhang, Xiao-hui [1 ,2 ,3 ]
Liu, Kai-yan [1 ,2 ,3 ]
Huang, Xiao-jun [1 ,2 ,3 ,4 ]
机构
[1] Peking Univ Peoples Hosp, Peking Univ Inst Hematol, Beijing 100044, Peoples R China
[2] Natl Clin Res Ctr Hematol Dis, Beijing 100044, Peoples R China
[3] Beijing Key Lab Hematopoiet Stem Cell Transplanta, Beijing 100044, Peoples R China
[4] Peking Tsinghua Ctr Life Sci, Beijing 100044, Peoples R China
基金
中国国家自然科学基金;
关键词
acute myeloid leukemia; allogeneic hematopoietic stem cell transplantation; refractory; relapsed; total therapy; STEM-CELL TRANSPLANTATION; VERSUS-HOST-DISEASE; STAGE ACUTE-LEUKEMIA; MARROW TRANSPLANTATION; HEMATOPOIETIC SCT; ADULT PATIENTS; WORKING PARTY; BLOOD; DLI; PREVENTION;
D O I
10.1002/cac2.12376
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background Patients with refractory or relapsed acute myeloid leukemia (AML) have poor survival, necessitating the exploration of optimized therapeutic strategy. Here, we aimed to investigate clinical outcomes and health-related quality of life (HR-QoL) after total therapy, which included allogeneic hematopoietic stem cell transplantation (allo-HSCT), and prophylactic donor lymphocyte infusion (DLI) in the early phase after transplantation, followed by multiple measurable residual disease (MRD) and graft-versus-host disease (GvHD)-guided DLIs. Methods Consecutive patients who had refractory or relapsed AML and had received non-T-cell-depleted allo-HSCT at Peking University Institute of Hematology were included in the study. If the patients achieved complete remission at 30 days after transplantation and had no evidence of relapse, severe infection, organ failure, and active GvHD at the time of planned DLI, prophylactic DLI was administered at 30 days after transplantation for human leukocyte antigen (HLA)-matched related HSCT or at 45-60 days after transplantation for haploidentical or unrelated HSCT. Subsequently, multiple DLIs were administered based on MRD results and whether they developed GvHD after transplantation. Results A total of 105 patients were eligible. Eighty-seven patients received prophylactic DLI (group B), while 18 did not receive prophylactic DLI (group A). Among 105 patients, the cumulative incidence of grade 2-4 acute GvHD and chronic GvHD was 40.6% (95% confidence interval [CI] = 30.6%-50.6%) and 73.3% (95% CI = 67.4%-79.2%), respectively. The cumulative incidence of relapse (CIR), transplant-related mortality (TRM), and leukemia-free survival (LFS) at 5 years after transplantation were 31.5% (95% CI = 21.9%-41.1%), 22.1% (95% CI = 11.3%-32.9%), and 46.4% (95% CI = 36.8%-56.0%), respectively. In group B, the CIR, TRM, and LFS at 5 years after transplantation were 27.6% (95% CI = 17.6%-37.6%), 21.6% (95% CI = 11.2%-32.0%), and 50.8% (95% CI = 40.0%-61.6%), respectively. At the end of follow-up, 48 patients survived, and more than 90% of survivors had satisfactory recoveries of HR-QoL. Conclusions Our study indicated that total therapy is not only associated with decreased CIR, comparable TRM, and better long-term LFS, but also with satisfactory HR-QoL for refractory or relapsed AML, compared with those of standard of care therapy reported previously. Therefore, total therapy may be an optimized therapeutic strategy for refractory or relapsed AML.
引用
收藏
页码:1387 / 1402
页数:16
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