Next-generation biomarkers for cancer-associated thrombosis prediction: the role of non-genomic-omics

Prediction of cancer-associated thrombosis (CAT) remains a major clinical challenge. Although genomic data and clinic-genetic scores have advanced understanding, they do not explain all inter-individual variability in CAT risk. Non-genomic omics, including proteomics, transcriptomics and epigenomics, capture complementary, dynamic biological information that can improve risk stratification. In summary, genomics contributes one piece of a much larger puzzle, necessary, informative, but fundamentally insufficient when used alone to understand, predict or manage CAT. This review synthesizes recent evidence on these non-genomic–omics for CAT prediction, highlights current limitations (validation, standardization, causal inference) and outlines priorities for translational development and clinical validation.

Authors

Publication Details

Journal
Bleeding Thrombosis and Vascular Biology
Published
2026-04-16
DOI
https://doi.org/10.4081/btvb.2026.447
Primary Topic
Venous Thromboembolism Diagnosis and Management
Type
article
Field-Weighted Citation Impact
0.00
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article

Next-generation biomarkers for cancer-associated thrombosis prediction: the role of non-genomic-omics

José Manuel Soria, Andrés Muñoz, Joan Carles Souto
Bleeding Thrombosis and Vascular Biology
Venous Thromboembolism Diagnosis and Management
article

Next-generation biomarkers for cancer-associated thrombosis prediction: the role of non-genomic-omics

José Manuel Soria, Andrés Muñoz, Joan Carles Souto
article en

Abstract

Prediction of cancer-associated thrombosis (CAT) remains a major clinical challenge. Although genomic data and clinic-genetic scores have advanced understanding, they do not explain all inter-individual variability in CAT risk. Non-genomic omics, including proteomics, transcriptomics and epigenomics, capture complementary, dynamic biological information that can improve risk stratification. In summary, genomics contributes one piece of a much larger puzzle, necessary, informative, but fundamentally insufficient when used alone to understand, predict or manage CAT. This review synthesizes recent evidence on these non-genomic–omics for CAT prediction, highlights current limitations (validation, standardization, causal inference) and outlines priorities for translational development and clinical validation.

Bleeding Thrombosis and Vascular BiologyVol. 5(s1)
Openalex Percentile: Top 23%
Venous Thromboembolism Diagnosis and Management
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