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RE-STRATIFYING THE PROGNOSES OF ACUTE MYELOID LEUKEMIA PATIENTS WITH CEBPA DOUBLE MUTATIONS BY CSF3R MUTATIONS AND MINIMAL RESIDUAL DISEASE
Author(s): ,
Long Su
Affiliations:
Department of Hematology,The First Hospital of Jilin University,Changchun,China
,
YeHui Tan
Affiliations:
Department of Hematology,The First Hospital of Jilin University,Changchun,China
,
JingNan Sun
Affiliations:
Department of Hematology,The First Hospital of Jilin University,Changchun,China
,
Hai Lin
Affiliations:
Department of Hematology,The First Hospital of Jilin University,Changchun,China
,
QiuJu Liu
Affiliations:
Department of Hematology,The First Hospital of Jilin University,Changchun,China
,
ChunShui Liu
Affiliations:
Department of Hematology,The First Hospital of Jilin University,Changchun,China
,
Yan Yang
Affiliations:
Department of Hematology,The First Hospital of Jilin University,Changchun,China
Sujun Gao
Affiliations:
Department of Hematology,The First Hospital of Jilin University,Changchun,China
EHA Library. Gao S. 06/09/21; 325229; EP469
SuJun Gao
SuJun Gao
Contributions
Abstract
Presentation during EHA2021: All e-poster presentations will be made available as of Friday, June 11, 2021 (09:00 CEST) and will be accessible for on-demand viewing until August 15, 2021 on the Virtual Congress platform.

Abstract: EP469

Type: E-Poster Presentation

Session title: Acute myeloid leukemia - Clinical

Background
Although AML with CEBPAdm indicates a favorable outcome, both our study and data from other studies showed that approximate half of the patients finally relapsed consolidated with chemotherapy alone. Therefore, the heterogeneity of acute myeloid leukemia (AML) with CEBPAdm attracts much attention in recent years.

Aims
The aim of this study was to evaluate the influence of CSF3R mutations and chemosensitivity indexes on prognoses of AML patients with CEBPAdm.

Methods
Sixty-six AML patients with complete genetic mutations and sequential minimal residual disease (MRD) information were retrospectively analyzed in this study.

Results
In AML patients with CSF3R mutations, 56.25% (9/16) of the patients achieving negative MRD after two courses of chemotherapy, which was significantly lower than those without mutation (82.00%, 41/50, P = 0.049). Both CSF3R mutations and MRD status after the second course of chemotherapy associated with long-term outcomes of patients. CSF3R mutated patients showed inferior relapse-free survival (RFS) (5-year RFS: 15.19% vs. 38.7%, P = 0.006) and overall survival (OS) (5-year OS: 8.2% vs. 60.6%, P = 0.038) compared with those with wide-type CSF3R. Negative MRD after the second course of chemotherapy was also an unfavorable indictor for both RFS (5-year RFS: 0.00% vs. 45.5%, P = 0.004) and OS (5-year OS: 0.00% vs. 65.4%, P = 0.050). Finally, a new prognostic model was proposed for AML with CEBPAdm in this study.

Conclusion
Both CSF3R mutations and positive MRD after the second course of chemotherapy were associated with poor outcomes for AML patients with CEBPAdm. An integrity model based on CSF3R mutations and MRD status may be beneficial for evaluating the prognoses of these patients.

Keyword(s):

Presentation during EHA2021: All e-poster presentations will be made available as of Friday, June 11, 2021 (09:00 CEST) and will be accessible for on-demand viewing until August 15, 2021 on the Virtual Congress platform.

Abstract: EP469

Type: E-Poster Presentation

Session title: Acute myeloid leukemia - Clinical

Background
Although AML with CEBPAdm indicates a favorable outcome, both our study and data from other studies showed that approximate half of the patients finally relapsed consolidated with chemotherapy alone. Therefore, the heterogeneity of acute myeloid leukemia (AML) with CEBPAdm attracts much attention in recent years.

Aims
The aim of this study was to evaluate the influence of CSF3R mutations and chemosensitivity indexes on prognoses of AML patients with CEBPAdm.

Methods
Sixty-six AML patients with complete genetic mutations and sequential minimal residual disease (MRD) information were retrospectively analyzed in this study.

Results
In AML patients with CSF3R mutations, 56.25% (9/16) of the patients achieving negative MRD after two courses of chemotherapy, which was significantly lower than those without mutation (82.00%, 41/50, P = 0.049). Both CSF3R mutations and MRD status after the second course of chemotherapy associated with long-term outcomes of patients. CSF3R mutated patients showed inferior relapse-free survival (RFS) (5-year RFS: 15.19% vs. 38.7%, P = 0.006) and overall survival (OS) (5-year OS: 8.2% vs. 60.6%, P = 0.038) compared with those with wide-type CSF3R. Negative MRD after the second course of chemotherapy was also an unfavorable indictor for both RFS (5-year RFS: 0.00% vs. 45.5%, P = 0.004) and OS (5-year OS: 0.00% vs. 65.4%, P = 0.050). Finally, a new prognostic model was proposed for AML with CEBPAdm in this study.

Conclusion
Both CSF3R mutations and positive MRD after the second course of chemotherapy were associated with poor outcomes for AML patients with CEBPAdm. An integrity model based on CSF3R mutations and MRD status may be beneficial for evaluating the prognoses of these patients.

Keyword(s):

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