TY - JOUR
T1 - Allogeneic stem cell transplantation in de novo core-binding factor acute myeloid leukemia in first complete remission
T2 - data from the EBMT
AU - Al Hamed, Rama
AU - Labopin, Myriam
AU - Wu, Depei
AU - Gedde-Dahl, Tobias
AU - Aljurf, Mahmoud
AU - Forcade, Edouard
AU - Salmenniemi, Urpu
AU - Passweg, Jakob
AU - Maertens, Johan
AU - Pabst, Thomas
AU - Versluis, Jurjen
AU - Itala-Remes, Maija
AU - Huang, Xiao-Jun
AU - Van Gorkom, Gwendolyn
AU - Schroeder, Thomas
AU - Sanz, Jaime
AU - Blaise, Didier
AU - Remenyi, Peter
AU - Schanz, Urs
AU - Esteve, Jordi
AU - Gorin, Norbert-Claude
AU - Ciceri, Fabio
AU - Mohty, Mohamad
PY - 2024/8/1
Y1 - 2024/8/1
N2 - Core-binding factor acute myeloid leukemia (CBF-AML) represents 12-15% of all AML cases. Although CBF positivity infers a survival advantage, overall survival (OS) remains dismal. Treatment is with cytarabine/anthracycline-based chemotherapy induction followed by high-dose cytarabine (HiDAC) consolidation. Allogeneic hematopoietic stem cell transplantation (allo-SCT) is reserved for relapse or for patients having not achieved MRD-negativity at high risk for relapse. The role of SCT in first complete remission (CR1) remains controversial and is considered in high risk conditions. In this retrospective, multi-national, European Society for Blood and Marrow Transplantation (EBMT)-based study, we identified 1901 patients with de novo CBF-AML who received an allo-SCT or autologous transplantation (ASCT) in CR1. 65.5% harbored t(8;21) and 34.4% inv(16). In this group, the majority (77%) were treated with allo-SCT in CR1. In multivariate analysis, treatment with allo-SCT was an independent and significant, negative predictor of NRM and OS (HR 4.26, p < 0.0001 and HR 1.67, p = 0.003) and among patients treated with allo-SCT, those treated with MSD had the best outcomes, comparable to those treated with ASCT. There was no interaction between the type of transplant and MRD status at time of SCT. In both, MRD-negative and MRD-positive groups, NRM was worse in the allo-SCT group (MRD-: 12.9% vs 5.2%, p = 0.007; MRD+: 10.6% vs 0%, p = 0.004). We therefore demonstrated that consolidation in CR1 with allo-SCT results in worse outcomes than ASCT. Whether consolidation with ASCT yields better outcomes than chemotherapy alone or chemotherapy in combination with Gemtuzumab Ozogamicin is yet to be investigated.
AB - Core-binding factor acute myeloid leukemia (CBF-AML) represents 12-15% of all AML cases. Although CBF positivity infers a survival advantage, overall survival (OS) remains dismal. Treatment is with cytarabine/anthracycline-based chemotherapy induction followed by high-dose cytarabine (HiDAC) consolidation. Allogeneic hematopoietic stem cell transplantation (allo-SCT) is reserved for relapse or for patients having not achieved MRD-negativity at high risk for relapse. The role of SCT in first complete remission (CR1) remains controversial and is considered in high risk conditions. In this retrospective, multi-national, European Society for Blood and Marrow Transplantation (EBMT)-based study, we identified 1901 patients with de novo CBF-AML who received an allo-SCT or autologous transplantation (ASCT) in CR1. 65.5% harbored t(8;21) and 34.4% inv(16). In this group, the majority (77%) were treated with allo-SCT in CR1. In multivariate analysis, treatment with allo-SCT was an independent and significant, negative predictor of NRM and OS (HR 4.26, p < 0.0001 and HR 1.67, p = 0.003) and among patients treated with allo-SCT, those treated with MSD had the best outcomes, comparable to those treated with ASCT. There was no interaction between the type of transplant and MRD status at time of SCT. In both, MRD-negative and MRD-positive groups, NRM was worse in the allo-SCT group (MRD-: 12.9% vs 5.2%, p = 0.007; MRD+: 10.6% vs 0%, p = 0.004). We therefore demonstrated that consolidation in CR1 with allo-SCT results in worse outcomes than ASCT. Whether consolidation with ASCT yields better outcomes than chemotherapy alone or chemotherapy in combination with Gemtuzumab Ozogamicin is yet to be investigated.
KW - INDIVIDUAL PATIENT DATA
KW - VERSUS-HOST-DISEASE
KW - RISK STRATIFICATION
KW - ADULT PATIENTS
KW - RELAPSE
KW - T(8/21)
KW - MARROW
KW - ABNORMALITIES
KW - CHEMOTHERAPY
KW - METAANALYSIS
U2 - 10.1038/s41409-024-02373-5
DO - 10.1038/s41409-024-02373-5
M3 - Article
SN - 0268-3369
JO - Bone Marrow Transplantation
JF - Bone Marrow Transplantation
ER -