Inferior outcome of allogeneic stem cell transplantation for secondary acute myeloid leukemia in first complete remission as compared to de novo acute myeloid leukemia

被引:39
|
作者
Schmaelter, Ann-Kristin [1 ]
Labopin, Myriam [2 ,3 ]
Socie, Gerard [4 ]
Itala-Remes, Maija [5 ]
Blaise, Didier [6 ]
Yakoub-Agha, Ibrahim [7 ]
Forcade, Edouard [8 ]
Cornelissen, Jan [9 ]
Ganser, Arnold [10 ]
Beelen, Dietrich [11 ]
Labussiere-Wallet, Helene [12 ]
Passweg, Jakob [13 ]
Savani, Bipin N. [14 ]
Schmid, Christoph [1 ]
Nagler, Arnon [3 ,15 ]
Mohty, Mohamad [2 ]
机构
[1] Augsburg Univ Hosp, Dept Hematol & Oncol, Augsburg, Germany
[2] Univ Paris 06, St Antoine Hosp, INSERM, Dept Haematol,UMR 938, Paris, France
[3] EBMT Paris Study Off CEREST TC, Paris, France
[4] Hop St Louis, Dept Hematol BMT, Paris, France
[5] HUCH Comprehens Canc Ctr, Stem Cell Transplantat Unit, Helsinki, Finland
[6] Inst Paoli Calmettes, Ctr Rech Cancerol Marseille, Programme Transplantat & Therapie Cellulaire, Marseille, France
[7] Univ Lille, CHU Lille, INSERM, LIRIC,U995, F-59000 Lille, France
[8] CHU Bordeaux, Hop Haut Leveque, Pessac, France
[9] Univ Med Ctr Rotterdam, Erasmus MC Canc Inst, Dept Hematol, Rotterdam, Netherlands
[10] Hannover Med Sch, Dept Haematol Hemostasis Oncol & Stem Cell Transp, Hannover, Germany
[11] Univ Hosp, Dept Bone Marrow Transplantat, Essen, Germany
[12] Ctr Hosp Lyon Sud, Serv Hematol, Lyon, France
[13] Univ Hosp, Hematol, Basel, Switzerland
[14] Vanderbilt Univ, Med Ctr, Div Hematol Oncol, Nashville, TN USA
[15] Chaim Sheba Med Ctr, Hematol Div, Tel Hashomer, Israel
关键词
AML; THERAPY; SURVIVAL; CYTOGENETICS; RELAPSE;
D O I
10.1038/s41408-020-0296-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Following chemotherapy, secondary acute myeloid leukemia (sAML), occurring after antecedent hematologic diseases, previous chemotherapy or radiation, has an inferior prognosis compared with de novo AML. To define the outcome of sAML in the context of allogeneic stem cell transplantation (alloSCT), a retrospective, registry-based comparison was performed, including 11,439 patients with de novo and 1325 with sAML. Among transplants in first complete remission (CR1) (n = 8,600), the 3-year cumulative incidence of relapse (RI) and non-relapse mortality (NRM) was 28.5% and 16.4% for de novo, and 35% and 23.4% for sAML. Three-year overall survival (OS), leukemia-free survival (LFS) and Graft-versus-Host Disease/relapse-free survival (GRFS) was 60.8%, 55.1%, and 38.6% for de novo, and 46.7%, 41.6%, and 28.4% for sAML, respectively. In multivariate analysis, sAML was associated with a lower OS (HR = 1.33 [95% CI = 1.21-1.48]; p < 10(-5)), LFS (HR = 1.32 [95% CI = 1.19-1.45]; p < 10(-5)) and GRFS (HR = 1.2 [95% CI = 1.1-1.31]; p < 10(-4)) and higher NRM (HR = 1.37 [95% CI = 1.17-1.59]; p < 10(-4)) and RI (HR = 1.27 [95% CI = 1.12-1.44]; p < 10(-3)). Results of the Cox model were confirmed in a matched-pair analysis. In contrast, results did not differ between de novo and sAML after alloSCT in induction failure or relapse. Hence, this analysis identified sAML as an independent risk factor for outcome after alloSCT in CR1.
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页数:9
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