Abstract PS1-09-27: Breast Cancer and Brain Metastases: A 13-Year Single-Centre Experience in a Diverse UK Population

Abstract Background: Brain metastases (BM) affect approximately 30-35% of patients with metastatic breast cancer (MBC), significantly worsening prognosis and quality of life1. Although therapeutic options have expanded, real-world UK data describing the patterns of BM and their association with tumour subtypes and outcomes remain limited. Objectives: To characterise the clinicopathological features, treatment patterns, and survival outcomes of patients with breast cancer and BM at a single UK centre over a 13-year period, with a focus on breast cancer subtype distribution and associated prognoses. Methods: This was a retrospective study of 261 patients reviewed via the University Hospitals of Leicester NHS Trust brain metastasis registry on Ledidi between December 2011 and December 2024. Patients were included if imaging confirmed brain metastases; 14 were excluded due to incomplete or non-confirmatory imaging. Clinical data were extracted via manual review of electronic records. Subtypes were defined per ASCO/CAP guidelines (ER/HER2 status). Descriptive statistics were used to summarise baseline characteristics. Overall survival (OS) from BM diagnosis was calculated using medians and interquartile ranges (IQR), and statistical comparisons across subtypes were performed. Results: The final cohort included 247 patients. Median age was 57 years. Ethnic distribution: 81% White, 14% Asian, 3% Black. Most patients (83%) presented symptomatically; 88% had concurrent extracranial disease (74% visceral; 67% bone). Initial imaging: CT (53%), MRI (37%). Subtype breakdown: ER+/HER2- (40.5%), ER-/HER2- (27%), ER+/HER2+ (16%), ER-/HER2+ (12.7%). Median OS from BM diagnosis was 17 weeks (IQR 5-42). Survival varied significantly by subtype (p<0.01): ER-/HER2+ (40.5 weeks) ER+/HER2+ (31 weeks) ER+/HER2- (14 weeks) ER-/HER2- (9 weeks) Patients received a median of two systemic treatment lines (IQR 1-3; maximum 7). Whole-brain radiotherapy (WBRT) was the most common treatment (32%), followed by stereotactic radiosurgery (SRS) in 19.4%; treatment data were unavailable for 27.5%. Conclusions: In this large single-centre UK cohort, ER+/HER2- was the most frequent subtype, while ER-/HER2- was associated with the poorest prognosis. HER2+ subtypes showed superior outcomes, reflecting improved therapeutic options. These findings support the need for earlier brain surveillance in high-risk subtypes and underscore brain metastases as an area of unmet need in breast cancer management. References: 1. Akshara S. Raghavendra et al. Breast Cancer Brain Metastasis: A Comprehensive Review. JCO Oncol Pract 20, 1348-1359(2024). DOI:10.1200/OP.23.00794 Citation Format: S. Goyal, F. Mutamba, M. Aamir, A. Tucker, E. Hurley, K. Sampson, B. Varadhan, L. Balakrishnan, S. Ahmed, O. Ayodele. Breast Cancer and Brain Metastases: A 13-Year Single-Centre Experience in a Diverse UK Population [abstract]. In: Proceedings of the San Antonio Breast Cancer Symposium 2025; 2025 Dec 9-12; San Antonio, TX. Philadelphia (PA): AACR; Clin Cancer Res 2026;32(4 Suppl):Abstract nr PS1-09-27.

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Clinical Cancer Research
Published
2026-02-17
DOI
https://doi.org/10.1158/1557-3265.sabcs25-ps1-09-27
Primary Topic
Brain Metastases and Treatment
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article
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article

Abstract PS1-09-27: Breast Cancer and Brain Metastases: A 13-Year Single-Centre Experience in a Diverse UK Population

Olubukola Ayodele, Balaji Varadhan, Kufre Sampson, M. Aamir et al.
Clinical Cancer Research
Brain Metastases and Treatment
article

Abstract PS1-09-27: Breast Cancer and Brain Metastases: A 13-Year Single-Centre Experience in a Diverse UK Population

Olubukola Ayodele, Balaji Varadhan, Kufre Sampson, M. Aamir, E. Hurley, S. Ahmed, S. Goyal, F. Mutamba, L. Balakrishnan, A. Tucker
article en

Abstract

Abstract Background: Brain metastases (BM) affect approximately 30-35% of patients with metastatic breast cancer (MBC), significantly worsening prognosis and quality of life1. Although therapeutic options have expanded, real-world UK data describing the patterns of BM and their association with tumour subtypes and outcomes remain limited. Objectives: To characterise the clinicopathological features, treatment patterns, and survival outcomes of patients with breast cancer and BM at a single UK centre over a 13-year period, with a focus on breast cancer subtype distribution and associated prognoses. Methods: This was a retrospective study of 261 patients reviewed via the University Hospitals of Leicester NHS Trust brain metastasis registry on Ledidi between December 2011 and December 2024. Patients were included if imaging confirmed brain metastases; 14 were excluded due to incomplete or non-confirmatory imaging. Clinical data were extracted via manual review of electronic records. Subtypes were defined per ASCO/CAP guidelines (ER/HER2 status). Descriptive statistics were used to summarise baseline characteristics. Overall survival (OS) from BM diagnosis was calculated using medians and interquartile ranges (IQR), and statistical comparisons across subtypes were performed. Results: The final cohort included 247 patients. Median age was 57 years. Ethnic distribution: 81% White, 14% Asian, 3% Black. Most patients (83%) presented symptomatically; 88% had concurrent extracranial disease (74% visceral; 67% bone). Initial imaging: CT (53%), MRI (37%). Subtype breakdown: ER+/HER2- (40.5%), ER-/HER2- (27%), ER+/HER2+ (16%), ER-/HER2+ (12.7%). Median OS from BM diagnosis was 17 weeks (IQR 5-42). Survival varied significantly by subtype (p<0.01): ER-/HER2+ (40.5 weeks) ER+/HER2+ (31 weeks) ER+/HER2- (14 weeks) ER-/HER2- (9 weeks) Patients received a median of two systemic treatment lines (IQR 1-3; maximum 7). Whole-brain radiotherapy (WBRT) was the most common treatment (32%), followed by stereotactic radiosurgery (SRS) in 19.4%; treatment data were unavailable for 27.5%. Conclusions: In this large single-centre UK cohort, ER+/HER2- was the most frequent subtype, while ER-/HER2- was associated with the poorest prognosis. HER2+ subtypes showed superior outcomes, reflecting improved therapeutic options. These findings support the need for earlier brain surveillance in high-risk subtypes and underscore brain metastases as an area of unmet need in breast cancer management. References: 1. Akshara S. Raghavendra et al. Breast Cancer Brain Metastasis: A Comprehensive Review. JCO Oncol Pract 20, 1348-1359(2024). DOI:10.1200/OP.23.00794 Citation Format: S. Goyal, F. Mutamba, M. Aamir, A. Tucker, E. Hurley, K. Sampson, B. Varadhan, L. Balakrishnan, S. Ahmed, O. Ayodele. Breast Cancer and Brain Metastases: A 13-Year Single-Centre Experience in a Diverse UK Population [abstract]. In: Proceedings of the San Antonio Breast Cancer Symposium 2025; 2025 Dec 9-12; San Antonio, TX. Philadelphia (PA): AACR; Clin Cancer Res 2026;32(4 Suppl):Abstract nr PS1-09-27.

Clinical Cancer ResearchVol. 32(4_Supplement)
Leicester Royal Infirmary (GB), Lividi (Norway) (NO)
Openalex Percentile: Top 53%
Brain Metastases and Treatment
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