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Poster Display & Cocktail

103P - Molecular and immunohistochemical characterization of radiation-induced breast angiosarcoma

Date

03 Mar 2025

Session

Poster Display & Cocktail

Presenters

Duygu Erhan Keskin

Citation

Annals of Oncology (2025) 10 (suppl_2): 1-9. 10.1016/esmoop/esmoop104255

Authors

D. Erhan Keskin1, M.E. El-Asrag2, A. Shaaban3, V. Heath1, R. Bicknell1, A.D. Beggs4

Author affiliations

  • 1 Institute Of Cardiovascular Sciences, The University of Birmingham, Medical School, B15 2TT - Birmingham/GB
  • 2 College Of Health And Life Sciences, Aston University, B4 7ET - Birmingham/GB
  • 3 Histopathology, Queen Elizabeth Hospital - University Hospitals Birmingham NHS Foundation Trust, B15 2TH - Birmingham/GB
  • 4 Institute Of Cancer & Genomic Science, The University of Birmingham - Medical School, B15 2TT - Birmingham/GB

Resources

This content is available to ESMO members and event participants.

Abstract 103P

Background

Angiosarcomas are rare yet highly aggressive malignant tumours originating from vascular endothelial cells. Treatment options are limited, and early diagnosis is critical for patient management. They can be classified into primary and radiation-induced (secondary) angiosarcomas. Secondary angiosarcomas have not yet been fully elucidated in terms of pathogenesis, clinical behaviour, early diagnostic biomarkers, genetic abnormalities and treatment targets. Identification of new biomarkers and therapeutic targets is important for improving the diagnosis and treatment of secondary breast angiosarcomas. This study is focused on secondary breast angiosarcoma arising as a consequence of radiotherapy following breast cancer treatment. These typically occur 5 to 10 years after radiation therapy. The objective of this study was to elucidate the immunohistochemical (IHC) profile of secondary angiosarcoma and determine the gene expression pattern of secondary angiosarcoma by performing RNA-seq analysis.

Methods

CD34, CD31, FLI-1 and ERG IHC stains were performed on 8 paraffin-embedded breast tissue sections diagnosed as secondary angiosarcoma. A total of 19 fresh frozen tissues were used for the RNAseq analysis of which 13 samples were angiosarcoma tumour tissue, while 6 samples were healthy tissue.

Results

CD31, CD34, and FLI1 were consistently highly expressed across four of the eight tumour samples, whereas ERG positivity was detected in only one of these four samples. Additionally, one tumour sample exhibited positivity solely for CD34 and FLI1, indicating variability in the expression of endothelial markers across cases. In the RNAseq analyses, 644 differentially expressed genes (DEGs) were identified, with 72 genes upregulated and 572 downregulated in secondary breast angiosarcoma. Gene Ontology (GO) enrichment analysis revealed that these DEGs were predominantly associated with biological processes like metabolism, energy pathways, and protein metabolism.

Conclusions

The findings presented highlight the heterogeneity in the expression of endothelial markers and transcriptomic profiles in secondary breast angiosarcoma, contributing to our understanding of this rare and aggressive malignancy.

Clinical trial identification

Editorial acknowledgement

Legal entity responsible for the study

The authors.

Funding

Ministry of National Education of Turkey.

Disclosure

All authors have declared no conflicts of interest.

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