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December 8, 2025BloodOpen Access

A blood-based protein signature adds to genomic prognostication of survival in TP53-mutated Acute Myeloid Leukemia

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Authors

SLSanam LoghaviFHFadi HaddadGBGautam Borthakur

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Overview

Machine learning reveals a 13-protein signature adds prognostic value for survival in TP53-mutated AML, suggesting new therapeutic approaches.

Key Points

  • High-risk TP53-mutated AML patients showed a median overall survival of only 3 months, highlighting the urgent need for better prognostic tools.
  • Thirteen inflammatory proteins were significantly associated with survival outcomes, deriving a hazard ratio of 3.02 when combined with genomic factors.
  • Assessment using machine learning on a large protein panel improved risk stratification in TP53-mutated AML beyond traditional methods.
  • Integrating this protein signature with existing genomic models may guide future therapeutic approaches in managing high-risk AML.

Cite This Study

Loghavi et al. (2025) studied this question.

synapsesocial.com/papers/69362f574fa91c937236da40https://doi.org/10.1182/blood-2025-3503
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Inflammatory and metabolic gene signatures predict overall survival and response to venetoclax-based therapy in TP53 mutant AML2025
  2. 2Treatments and outcomes of adult patients with TP53-mutated acute myeloid leukemia (AML) in the real-life –Report of the prospective french observational ALFA-PPP study.2025 · 1 citations
  3. 3High levels of PTPN11 protein are prognostically adverse and independent of mutation status in acute myelogenous leukemia2025
  4. 4Integrative omics analysis of TP53 in multiple myeloma patients2025
  5. 5A novel prognostic signature integrating disulfidptosis- and ferroptosis-related genes in acute myeloid leukemia2025 · 1 citations