Javascript must be enabled to continue!
Clinical and Prognostic Significance of CEBPA Mutations in Myelodysplastic Syndromes
View through CrossRef
Background/Objectives: Myelodysplastic syndromes (MDS) carry a highly variable prognosis, stratified by the Revised International Prognostic Scoring System (IPSS-R) and the Molecular IPSS (IPSS-M). CEBPA mutations define a favorable-risk subgroup in acute myeloid leukemia (AML), yet their prognostic significance in MDS has not been characterized. Methods: We analyzed 2442 patients from the International Working Group (IWG) 2022 multi-center MDS registry after pre-specified exclusions. Overall survival (OS) and leukemia-free survival (LFS) were compared between CEBPA-mutated (n = 66; 2.7%) and wild-type patients using Kaplan–Meier estimation and Cox proportional hazards regression, adjusting for age, sex, and IPSS-R score; pre-specified subgroup, sensitivity, competing-risk, and mutation subtype analyses were performed. Results:CEBPA-mutated patients had markedly inferior OS (median 17.2 versus 42.2 months; HR 2.05, 95% CI 1.50–2.79; p < 0.001). After IPSS-R adjustment, the hazard ratio remained adverse (HR 1.39, 95% CI 1.00–1.94; p = 0.053), with uniform directionality across all 13 evaluable subgroups and no significant interaction. Co-mutation adjustment for ASXL1 and STAG2 further attenuated the hazard ratio to HR 1.11 (95% CI 0.79–1.57; p = 0.54), suggesting part of the observed signal reflects co-mutation burden rather than an independent CEBPA effect. Competing-risk analysis suggested that the excess mortality is mediated through AML transformation (CEBPA-mutated versus wild-type subdistribution hazard ratio of 1.89, 95% CI 1.20–2.99; p = 0.006) rather than non-transformative MDS mortality (cause-specific HR 0.97; p = 0.890). Truncating mutations drove the adverse signal (HR 2.21; p = 0.023), while basic leucine zipper (bZIP) domain mutations showed no significant effect (HR 1.25; p = 0.470). Conclusions:CEBPA mutations identify a rare MDS subgroup with markedly inferior survival, driven by truncating loss-of-function mutations and associated with leukemic transformation; the AML-derived bZIP-favorable paradigm does not translate to MDS, and CEBPA mutation status merits a prospective study to assess clinical utility for risk stratification.
Title: Clinical and Prognostic Significance of CEBPA Mutations in Myelodysplastic Syndromes
Description:
Background/Objectives: Myelodysplastic syndromes (MDS) carry a highly variable prognosis, stratified by the Revised International Prognostic Scoring System (IPSS-R) and the Molecular IPSS (IPSS-M).
CEBPA mutations define a favorable-risk subgroup in acute myeloid leukemia (AML), yet their prognostic significance in MDS has not been characterized.
Methods: We analyzed 2442 patients from the International Working Group (IWG) 2022 multi-center MDS registry after pre-specified exclusions.
Overall survival (OS) and leukemia-free survival (LFS) were compared between CEBPA-mutated (n = 66; 2.
7%) and wild-type patients using Kaplan–Meier estimation and Cox proportional hazards regression, adjusting for age, sex, and IPSS-R score; pre-specified subgroup, sensitivity, competing-risk, and mutation subtype analyses were performed.
Results:CEBPA-mutated patients had markedly inferior OS (median 17.
2 versus 42.
2 months; HR 2.
05, 95% CI 1.
50–2.
79; p < 0.
001).
After IPSS-R adjustment, the hazard ratio remained adverse (HR 1.
39, 95% CI 1.
00–1.
94; p = 0.
053), with uniform directionality across all 13 evaluable subgroups and no significant interaction.
Co-mutation adjustment for ASXL1 and STAG2 further attenuated the hazard ratio to HR 1.
11 (95% CI 0.
79–1.
57; p = 0.
54), suggesting part of the observed signal reflects co-mutation burden rather than an independent CEBPA effect.
Competing-risk analysis suggested that the excess mortality is mediated through AML transformation (CEBPA-mutated versus wild-type subdistribution hazard ratio of 1.
89, 95% CI 1.
20–2.
99; p = 0.
006) rather than non-transformative MDS mortality (cause-specific HR 0.
97; p = 0.
890).
Truncating mutations drove the adverse signal (HR 2.
21; p = 0.
023), while basic leucine zipper (bZIP) domain mutations showed no significant effect (HR 1.
25; p = 0.
470).
Conclusions:CEBPA mutations identify a rare MDS subgroup with markedly inferior survival, driven by truncating loss-of-function mutations and associated with leukemic transformation; the AML-derived bZIP-favorable paradigm does not translate to MDS, and CEBPA mutation status merits a prospective study to assess clinical utility for risk stratification.
Related Results
Identifying PTPRJ As a Novel Mediator of CEBPA-Mutated AML
Identifying PTPRJ As a Novel Mediator of CEBPA-Mutated AML
10-20% of acute myeloid leukaemia (AML) cases in children and adults carry mutations in the transcription factor CCAAT/enhancer binding protein alpha (CEBPA). CEBPA is transcribed ...
CEBPA Gene Different Mutants Play Distinct Impacts On Tumor Suppressor Function Of C/EBP-Alpha and Bone Marrow Stromal Cells
CEBPA Gene Different Mutants Play Distinct Impacts On Tumor Suppressor Function Of C/EBP-Alpha and Bone Marrow Stromal Cells
Abstract
Introduction
CEBPA gene encodes CCAAT/enhancer-binding protein-alpha (C/EBPα), a crucial granulocytic differentiation f...
Risk Assessment in Patients with Acute Myeloid Leukemia and a Normal Karyotype
Risk Assessment in Patients with Acute Myeloid Leukemia and a Normal Karyotype
Abstract
Purpose: The recognition of a number of leukemia-specific cytogenetic abnormalities and their role as independent prognostic factors have provided considera...
Cdk6 targeting reverses leukemia in germline cebpa Q83X AML mouse model with CMP-origin transformation
Cdk6 targeting reverses leukemia in germline cebpa Q83X AML mouse model with CMP-origin transformation
Abstract
CEBPA mutations are frequent drivers of familial AML (FAML) and common in sporadic disease. While bZIP-in-frame...
High Resolution Melt Analysis for Rapid and Cost-Effective Screening of TP53 Mutations in Patients with Myeloid Malignancies
High Resolution Melt Analysis for Rapid and Cost-Effective Screening of TP53 Mutations in Patients with Myeloid Malignancies
Abstract
Background
Recent reports have highlighted an adverse impact of TP53 mutations on the prognosis of patients with myeloid malignancies. TP53 m...
Clinical and Biological Implications of CUX1 Mutations in Myeloid Neoplasms
Clinical and Biological Implications of CUX1 Mutations in Myeloid Neoplasms
Abstract
Recurrent somatic mutations of CUX1 are described in myeloid neoplasms. CUX1 is located at chromosome 7q22.1; -7/del(7q) involving CUX1 locus are common abn...
Crebbp HAT Domain Mutations Are Frequently Detected in Adult Acute Lymphoblastic Leukemia
Crebbp HAT Domain Mutations Are Frequently Detected in Adult Acute Lymphoblastic Leukemia
Abstract
Abstract 1419
Aims:
Molecular pathogenesis of acute lymphoblastic leukemia (ALL) has largely been verifi...
Dynamics of Mutations in Patients with ET Treated with Imetelstat
Dynamics of Mutations in Patients with ET Treated with Imetelstat
Abstract
Background: Imetelstat, a first in class specific telomerase inhibitor, induced hematologic responses in all patients (pts) with essential thrombocythemia (...

