Evidence map›Paper›PMID 42871535›Full record

ReviewFrontiers in pharmacology2026

AI-driven multi-omics biomarkers in precision breast cancer therapeutics: from discovery to clinical translation.

Dimitrios Stylianakis, Rodrigo Sánchez-Bayona, Nerina Denaro, Cinzia Solinas

Abstract readReview
In one paragraph

Review in Frontiers in pharmacology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Dimitrios StylianakisUniversity Hospital, Heraklion, Greece.
Rodrigo Sánchez-BayonaMedical Oncology Department, Hospital Universitario 12 de Octubre, Madrid, Spain.
Nerina DenaroMedical Oncology Unit, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico, Milan, Italy.
Cinzia SolinasMedical Oncology Unit, University Hospital of Cagliari, Cagliari, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Breast cancer is biologically heterogeneous, yet conventional clinical decisions rely on static, single-marker proxies (ER, PR, HER2, and Ki-67) that capture only a narrow slice of tumor biology. This mini-review argues that AI-driven multi-omics biomarkers offer a valuable shift toward systems-level, model-derived probabilities integrating genomic, transcriptomic, proteomic, metabolomic, and imaging information to explain and predict disease behavior more faithfully. We synthesize recent advances across three domains: (i) computational strategies for multi-omics integration, from classical penalized regression and ensemble learning to deep multimodal architectures and foundation-model embeddings; (ii) therapeutically relevant biomarker classes across tissue, liquid biopsy, and imaging modalities; and (iii) emerging pathways for embedding these biomarkers into clinical decision support. We highlight validation, interpretability, and robust handling of missing modalities as prerequisites for clinical trust, and outline how biomarker-driven trials, standardized reporting (e.g., TRIPOD + AI), and privacy-preserving data consortia can move AI-driven multi-omics biomarkers toward clinical and regulatory maturity.

Indexed as

artificial intelligencebiomarkersbreast cancerclinical translationmultiomicsprecision therapeutics

Identifiers

PMID42871535
PMCPMC13659096

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.