Biomarker prediction of immunotherapy response in breast cancer: from single markers to multi-omics integration

Immunotherapy has redefined treatment paradigms across several malignancies, yet its application in breast cancer remains limited to select subtypes, particularly triple-negative breast cancer. As immune checkpoint inhibitors advance into earlier disease stages and broader clinical use, the identification of predictive biomarkers is essential to optimize patient selection and therapeutic outcomes. This review critically examines the current landscape of immunotherapy biomarkers in breast cancer and discusses their predictive value across breast cancer subtypes and treatment settings, highlighting both their clinical relevance and limitations. While conventional single biomarkers have demonstrated clinical relevance, they remain limited in sensitivity and specificity. Recent data suggest that gene expression signatures may offer superior predictive power. Moreover, emerging evidence supports the utility of integrated, multi-parametric biomarker strategies that combine genomic, transcriptomic, spatial, and dynamic immune profiling. Ongoing endeavors in standardization, validation, and the incorporation of artificial intelligence-driven analytics are critical to translating these biomarkers into precision immuno-oncology for breast cancer.

Authors

Institutions

Publication Details

Journal
npj Breast Cancer
Published
2025-12-09
DOI
https://doi.org/10.1038/s41523-025-00873-1
Citations
1
Primary Topic
Cancer Immunotherapy and Biomarkers
Type
article
Field-Weighted Citation Impact
1.05
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Biomarker prediction of immunotherapy response in breast cancer: from single markers to multi-omics integration

Elham Nasrollahi, Daria Chelysheva, Ali Sanjari Moghaddam, Adam Brufsky et al.
1 citations
npj Breast Cancer
Cancer Immunotherapy and Biomarkers
1.05
article

Biomarker prediction of immunotherapy response in breast cancer: from single markers to multi-omics integration

Elham Nasrollahi, Daria Chelysheva, Ali Sanjari Moghaddam, Adam Brufsky, Kit Lu, Lovette Oji, Oyindamola Amosu, Anna Homeniuk
article en
1 citations

Abstract

Immunotherapy has redefined treatment paradigms across several malignancies, yet its application in breast cancer remains limited to select subtypes, particularly triple-negative breast cancer. As immune checkpoint inhibitors advance into earlier disease stages and broader clinical use, the identification of predictive biomarkers is essential to optimize patient selection and therapeutic outcomes. This review critically examines the current landscape of immunotherapy biomarkers in breast cancer and discusses their predictive value across breast cancer subtypes and treatment settings, highlighting both their clinical relevance and limitations. While conventional single biomarkers have demonstrated clinical relevance, they remain limited in sensitivity and specificity. Recent data suggest that gene expression signatures may offer superior predictive power. Moreover, emerging evidence supports the utility of integrated, multi-parametric biomarker strategies that combine genomic, transcriptomic, spatial, and dynamic immune profiling. Ongoing endeavors in standardization, validation, and the incorporation of artificial intelligence-driven analytics are critical to translating these biomarkers into precision immuno-oncology for breast cancer.

npj Breast CancerVol. 12(1)
UPMC Hillman Cancer Center (US), University of Pittsburgh Medical Center (US)
Openalex Percentile: Top 15%
Cancer Immunotherapy and Biomarkers
1.05
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.