Clinicogenomic Characterization of Inflammatory Breast Cancer

This study provides a comprehensive resource of somatic alterations in a large cohort of patients with metastatic IBC and non-IBC, highlighting genomic features associated with worse outcomes. Our findings reveal a significant enrichment of TP53 mutations, reinforcing its critical role in IBC pathogenesis. Few other distinct differences in IBC were observed, suggesting further investigations-beyond bulk sequencing of the somatic genome-are required to better understand the biology driving this aggressive disease.

Authors

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Publication Details

Journal
Clinical Cancer Research
Published
2025-05-16
DOI
https://doi.org/10.1158/1078-0432.ccr-24-2081
Citations
2
Primary Topic
Breast Cancer Treatment Studies
Type
article
Field-Weighted Citation Impact
1.87

Funders

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article

Clinicogenomic Characterization of Inflammatory Breast Cancer

Jennifer R. Bellon, Filipa C. Lynce, Gregory John Kirkner, Melissa E. Hughes et al.
2 citations
Clinical Cancer Research
Breast Cancer Treatment Studies
1.87
article

Clinicogenomic Characterization of Inflammatory Breast Cancer

Jennifer R. Bellon, Filipa C. Lynce, Gregory John Kirkner, Melissa E. Hughes, Faina Nakhlis, Janet Files, Ana C. Garrido-Castro, Beth Harrison, Andrew D. Cherniack, Ayesha Mohammed-Abreu, Nolan Priedigkeit, Brittany Bychkovsky, Neal I. Lindeman, Anne-Marie Feeney, Marie Claire Remolano, Nancy U. Lin, Liam F. Spurr, Bruce E. Johnson, Deborah Dillon, Sara M. Tolaney, Eric P. Winer, Romualdo Barroso‐Sousa, Yvonne Li, Tari A. King, Beth Overmoyer, Lynette M. Sholl, Robert Shue, Alinés Lebrón-Torres, Libby Grant, Sarah Strauss
article en
2 citations

Abstract

This study provides a comprehensive resource of somatic alterations in a large cohort of patients with metastatic IBC and non-IBC, highlighting genomic features associated with worse outcomes. Our findings reveal a significant enrichment of TP53 mutations, reinforcing its critical role in IBC pathogenesis. Few other distinct differences in IBC were observed, suggesting further investigations-beyond bulk sequencing of the somatic genome-are required to better understand the biology driving this aggressive disease.

Clinical Cancer ResearchVol. 31(14)
Broad Institute (US), Brigham and Women's Hospital (US), Harvard University (US), Cornell University (US), Dana-Farber Cancer Institute (US), Dana-Farber/Harvard Cancer Center (US), Hospital Universitário de Brasília (BR), Dana-Farber Brigham Cancer Center (US), Weill Cornell Medicine (US), Case Western Reserve University (US)
American Association for Cancer Research, Conquer Cancer Foundation, Pan-Massachusetts Challenge, Susan G. Komen
No poverty
Openalex Percentile: Top 15%
Breast Cancer Treatment Studies
1.87
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