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
相关论文
共 45 条
[41]   Monitoring of post-transplant CBFB-MYH11 as minimal residual disease, rather than KIT mutations, can predict relapseafter allogeneic haematopoietic cell transplantation inadults with inv(16) acute myeloid leukaemia [J].
Tang, Fei-Fei ;
Xu, Lan-Ping ;
Zhang, Xiao-Hui ;
Chen, Huan ;
Chen, Yu-Hong ;
Han, Wei ;
Wang, Yu ;
Yan, Chen-Hua ;
Sun, Yu-Qian ;
Mo, Xiao-Dong ;
Liu, Kai-Yan ;
Huang, Xiao-Jun .
BRITISH JOURNAL OF HAEMATOLOGY, 2018, 180 (03) :448-451
[42]   Measurable residual disease monitoring by NGS before allogeneic hematopoietic cell transplantation in AML [J].
Thol, Felicitas ;
Gabdoulline, Razif ;
Liebich, Alessandro ;
Klement, Piroska ;
Schiller, Johannes ;
Kandziora, Christian ;
Hambach, Lothar ;
Stadler, Michael ;
Koenecke, Christian ;
Flintrop, Madita ;
Pankratz, Mira ;
Wichmann, Martin ;
Neziri, Blerina ;
Buettner, Konstantin ;
Heida, Bennet ;
Klesse, Sabrina ;
Chaturvedi, Anuhar ;
Kloos, Arnold ;
Goehring, Gudrun ;
Schlegelberger, Brigitte ;
Gaidzik, Verena I. ;
Bullinger, Lars ;
Fiedler, Walter ;
Heim, Albert ;
Hamwi, Iyas ;
Eder, Matthias ;
Krauter, Juergen ;
Schlenk, Richard F. ;
Paschka, Peter ;
Doehner, Konstanze ;
Doehner, Hartmut ;
Ganser, Arnold ;
Heuser, Michael .
BLOOD, 2018, 132 (16) :1703-1713
[43]   Comparison of minimal residual disease as outcome predictor for AML patients in first complete remission undergoing myeloablative or nonmyeloablative allogeneic hematopoietic cell transplantation [J].
Walter, R. B. ;
Gyurkocza, B. ;
Storer, B. E. ;
Godwin, C. D. ;
Pagel, J. M. ;
Buckley, S. A. ;
Sorror, M. L. ;
Wood, B. L. ;
Storb, R. ;
Appelbaum, F. R. ;
Sandmaier, B. M. .
LEUKEMIA, 2015, 29 (01) :137-144
[44]   Significance of minimal residual disease before myeloablative allogeneic hematopoietic cell transplantation for AML in first and second complete remission [J].
Walter, Roland B. ;
Buckley, Sarah A. ;
Pagel, John M. ;
Wood, Brent L. ;
Storer, Barry E. ;
Sandmaier, Brenda M. ;
Fang, Min ;
Gyurkocza, Boglarka ;
Delaney, Colleen ;
Radich, Jerald P. ;
Estey, Elihu H. ;
Appelbaum, Frederick R. .
BLOOD, 2013, 122 (10) :1813-1821
[45]   Pre- and post-transplant quantification of measurable ('minimal') residual disease via multiparameter flow cytometry in adult acute myeloid leukemia [J].
Zhou, Y. ;
Othus, M. ;
Araki, D. ;
Wood, B. L. ;
Radich, J. P. ;
Halpern, A. B. ;
Mielcarek, M. ;
Estey, E. H. ;
Appelbaum, F. R. ;
Walter, R. B. .
LEUKEMIA, 2016, 30 (07) :1456-1464