# Survival outcomes and clinical characteristics of brain metastases from prostate cancer: A single-center analysis

**Authors:** Kurl Jamora, Adeodatus Vito Nicanor, Ayah Erjan, Marc Vincent Barcelona, Dana Keilty, Michael Yan, Aristotelis Kalyvas, Marc Bernstein, Paul Kongkham, Gelareh Zadeh, Eshetu Atenafu, Srinivas Raman, Alejandro Berlin, Charles Catton, Peter Chung, Barbara-Ann Millar, Normand Laperriere, Tatiana Conrad, David Shultz, Enrique Gutierrez-Valencia

PMC · DOI: 10.1093/noajnl/vdaf063 · Neuro-Oncology Advances · 2025-03-22

## TL;DR

Brain metastases from prostate cancer are rare and occur in advanced cases, often with other metastases and poor survival outcomes.

## Contribution

This study provides a detailed analysis of clinical features and survival outcomes for a rare condition: brain metastases from prostate cancer.

## Key findings

- Median overall survival after brain metastasis diagnosis was 9.4 months.
- Most patients had castrate-resistant prostate cancer and concurrent metastases.
- Treatment modality did not significantly affect survival outcomes.

## Abstract

Brain metastases (BrM) from prostate cancer (PC) are rare. This study sought to evaluate their prevalence, clinical features, treatment modalities, and survival outcomes.

From a database of BrM patients, we analyzed 28 cases of prostate cancer treated at our center between 2008 and 2023.

BrM from PC comprised 0.7% of cases. The majority of patients had high-risk features at PC diagnosis: median prostate-specific antigen (PSA) at diagnosis was 65.5 ng/ml (range: 3.9–784.7 ng/ml), 82% were Gleason grade group ≥ 4, and 68% had perineural invasion (PNI). At BrM diagnosis, 79% were castrate-resistant. Most patients had concurrent metastases, including bone (94%), lymph nodes (63%), or lung (6%). Fifty percent presented with a single brain lesion, and the median Graded Prognostic Assessment (GPA) score was 1.5 (range: 0.5–2.5). Patients commonly had radiographic brain edema (57%) and neurological symptoms (54%), whereas only 7% had seizures. Median overall survival (OS) was 9.4 months (95% CI: 4.8–14.8 months) after BrM diagnosis. An upward trend in OS was observed with higher GPA (P = .07). Treatment modalities, including surgery with adjuvant radiation, stereotactic radiosurgery, and whole brain radiotherapy, showed no significant difference in median OS (9.4, 10.1, and 11.0 months respectively, P = .79). OS did not significantly differ between patients with a single versus multiple BrM or patients with castrate-sensitive versus castrate-resistant PC.

BrMs from prostate cancer are rare and predominantly occur in patients with advanced, castrate-resistant disease, often accompanied by other metastases. This analysis enhances our understanding of the disease trajectory and informs treatment discussions.

## Linked entities

- **Diseases:** prostate cancer (MONDO:0005159)

## Full-text entities

- **Genes:** GYPA (glycophorin A (MNS blood group)) [NCBI Gene 2993] {aka CD235a, GPA, GPErik, GPSAT, HGpMiV, HGpMiXI}, FOLH1 (folate hydrolase 1) [NCBI Gene 2346] {aka FGCP, FOLH, GCP2, GCPII, NAALAD1, PSM}, KLK3 (kallikrein related peptidase 3) [NCBI Gene 354] {aka APS, KLK2A1, PSA, hK3}
- **Diseases:** adenocarcinoma (MESH:D000230), seizures (MESH:D012640), lung cancer (MESH:D008175), dural-based disease (MESH:D019292), CRPC (MESH:D064129), CSPC (MESH:D011471), small cell and non-small cell lung cancer (MESH:D002289), WBRT (MESH:C531766), edema (MESH:D004487), neurological symptoms (MESH:D009461), PNI (MESH:D052958), gastrointestinal cancer (MESH:D005770), headache (MESH:D006261), breast cancer (MESH:D001943), neuroendocrine (MESH:D018358), sensorimotor deficits (MESH:D020233), meningioma (MESH:D008579), renal cell carcinoma (MESH:D002292), vomiting (MESH:D014839), disease (MESH:D004194), BrM (MESH:D001932), nausea (MESH:D009325), death (MESH:D003643), brain lesion (MESH:D001927), SCC (MESH:D018288), brain metastasis (MESH:D009362), lymph node metastasis (MESH:D008207), lung, melanoma, (MESH:D008545), Cancer (MESH:D009369), brain edema (MESH:D001929)
- **Chemicals:** castrate (-), docetaxel (MESH:D000077143)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

28 references — full list in the complete paper: https://tomesphere.com/paper/PMC12082812/full.md

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Source: https://tomesphere.com/paper/PMC12082812