Prognostic value of CEBPA bZIP signatures in cytogenetically normal acute myeloid leukaemia
Recent studies revealed that CEBPA with basic leucine zipper (bZIP) in‐frame mutation ( CEBPA bZIP‐inf ) is the bona fide entity with a favourable prognosis in acute myeloid leukaemia. However, the mechanism by which the bZIP signatures influence risk stratification remains unclear. We identified 14...
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Published in | British journal of haematology |
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Main Authors | , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
26.05.2025
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Subjects | |
Online Access | Get full text |
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Summary: | Recent studies revealed that CEBPA with basic leucine zipper (bZIP) in‐frame mutation ( CEBPA bZIP‐inf ) is the bona fide entity with a favourable prognosis in acute myeloid leukaemia. However, the mechanism by which the bZIP signatures influence risk stratification remains unclear. We identified 141 patients with CEBPA bZIP‐inf . Variant allele fraction (VAF) (cumulative incidence of relapse [CIR], VAF high vs. VAF low , 74.0% vs. 27.0%, p < 0.001) and base change (≤ vs. >3 bases, 39.1% vs. 60.6%, p = 0.042) of bZIP mutations were associated with CIR. These two factors, along with the white blood cell count and measurable residual disease after first consolidation, could stratify patients into three risk subgroups (CIR, low vs. medium vs. high risk, 15.2% vs. 47.1% vs. 83.0%, p < 0.001). Compared with no transplantation, receiving a transplantation significantly decreased the relapse rates in medium‐risk (transplantation vs. no transplantation, 11.6% vs. 49.7%, p = 0.009) and high‐risk patients (5.6% vs. 84.1%, p < 0.001) but not low‐risk (0% vs. 15.2%, p = 0.220). However, only high‐risk patients could benefit from transplantation in terms of overall survival (100% vs. 59.7%, p = 0.003). Our study revealed the heterogeneity of CEBPA bZIP‐inf patients and suggested a risk‐adapted treatment modality. Transplantation is recommended for high‐risk patients and consolidation chemotherapy is recommended for low‐risk and medium‐risk patients. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0007-1048 1365-2141 1365-2141 |
DOI: | 10.1111/bjh.20164 |