Combination of disease burden before allogeneic transplantation and early post-transplant minimal residual disease predicts survival in patients with acute myeloid leukemia

被引:0
作者
Stock, Claudia Nunez-Torron [1 ,2 ,3 ,4 ]
Chillon, Carlos Jimenez [5 ]
Hernandez, Clara Lopez [6 ]
Moro, Fernando Martin [4 ,6 ]
Palomanes, Juan Marquet [4 ,6 ]
Villaespesa, Miguel Piris [4 ,6 ]
de Abia, Alejandro Luna [4 ,6 ]
Santiago, Ernesto Roldan [7 ]
Martin, Eulalia Rodriguez [7 ]
Rodriguez, Anabelle Chinea [4 ,6 ]
Gutierrez, Valentin Garcia [2 ,4 ,6 ]
Jimenez, Gemma Moreno [4 ,6 ]
Jimenez, Javier Lopez [2 ,4 ,6 ]
Puente, Pilar Herrera [2 ,4 ,6 ]
机构
[1] Hosp Univ Infanta Sofia, Dept Hematol & Hemoterapia, Ave Paseo Europa 34, Madrid 28702, Spain
[2] Univ Alcala Henares, Madrid, Spain
[3] Univ Europea Madrid, Madrid, Spain
[4] Hosp Univ Ramon & Cajal, Hematol & Hemotherapy Serv, Inst Ramon & Cajal Invest Sanitaria IRYCIS, Madrid, Spain
[5] Hosp Univ Gregorio Maranon, Dept Hematol & Hemoterapia, Madrid, Spain
[6] Hosp Univ Ramon & Cajal, Dept Hematol & Hemoterapia, Madrid, Spain
[7] Hosp Univ Ramon & Cajal, Dept Inmunol, Madrid, Spain
关键词
Acute myeloid leukemia; Allogeneic transplantation; Pretrasplantation disease burden; Minimal residual disease; multiparameter flow cytometry; HEMATOPOIETIC-CELL TRANSPLANTATION; FLOW-CYTOMETRY; REDUCED-INTENSITY; OUTCOMES; MRD; AML; RECOMMENDATIONS; DIAGNOSIS; RELAPSE; ADULTS;
D O I
10.1007/s00277-025-06325-x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The burden disease before allogeneic transplantation (HSCT) or the early post-transplant minimal residual disease (MRD) are both predictive parameters for relapse and post-HSCT survival in acute myeloid leukemia (AML). Nonetheless, the combination of both can provide more accurate information to identify high risk patients. To analyze the impact of pre-HSCT disease burden (MRD- vs. MRD + vs. active disease (AD), the early post-transplant MRD (posMRD + vs. posMRD-), and the combination of both pre- and post-HSCT disease status of the post-HSCT outcomes in AML patients. We retrospectively analyzed 173 patients with AML who underwent HSCT in a single institution, patients were classified according to pre-HSCT disease status, and post-HSCT MRD. MRD was measured by multiparameter flow cytometry using a cut-off of 0.1% for MRD+. The post-HSCT outcomes were analyzed based on the pre-transplant status, post-transplant status, and by combining both parameters. Patients with AD and MRD + before HSCT had worse 3y-event free (EFS) and overall survival (OS) than MRD- patients, due to a higher cumulative incidence of relapse (CIR). Also, patients with posMRD + had worse outcomes than posMRD- group. In the combined analysis, patient with MRD-/posMRD- had the best EFS and OS (3y-EFS 66.5%, 3y-OS 70.0%). Patients with MRD+/posMRD- have worse prognosis (3y-EFS 39.0%, 3y-OS 54.0%) and specially the group with AD/MRD- (3y-EFS 13.5%, 3y-OS 22.0%) and posMRD + regardless pre-HSCT disease status(3y-EFS 26.5%, 3y-OS 28.0%) had dismal OS and EFS. The combination of pre-HSCT disease burden and post-HSCT MRD measurements help us for identifying high-risk subgroups. Any level of pre-transplant disease (MRD+, and especially patients with active AD) is a risk factor, even when MRD- was achieved post-transplant. Patients with post-transplant MRD + also had an adverse prognosis. These should be target groups for implementing tailored pre- and post-transplant strategies to improve outcomes.
引用
收藏
页码:2469 / 2481
页数:13
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