Impact of stereotactic radiosurgery timing relative to immune checkpoint blockade administration on brain metastasis disease and radionecrosis outcomes
- Author(s)
- Mittal, A; Green, A; Fitzgerald, X; Spain, L; Phillips, C; Wirth, A; Haghighi, N; Plumridge, N; Li, M; Sia, J;
- Details
- Publication Year 2025-01,Volume 7,Issue #1,Page vdaf130
- Journal Title
- Neuro-Oncology Advances
- Abstract
- BACKGROUND: Whether stereotactic radiosurgery (SRS) and immune checkpoint blockade (ICB) for brain metastases (BrM) have a time window for synergistic efficacy and toxicity is unclear. We examined this question in a large, contemporary cohort of patients who received concurrent SRS and ICB. METHODS: Patients who received SRS for intact BrM within 1 month before to 6 months after an ICB cycle at a single center from 2018 to 2023 were included if they had no prior whole-brain radiotherapy or SRS to the same BrM. Intracranial progression-free survival (icPFS), local control (LC), distant brain control (DBC), overall survival (OS), and radionecrosis were analyzed by Kaplan-Meier and log-rank methods. Cox regression was used for uni/multivariable analysis (UVA/MVA). RESULTS: A total of 419 BrM, 170 treatment episodes, and 134 patients were analyzed. In total, 43% and 40% of patients had melanoma and non-small cell lung cancer. A shorter SRS-ICB interval significantly correlated with improved icPFS, LC, and OS, but not DBC. This was true when analyzed as either a categorical or continuous factor. On MVA, SRS-ICB interval outperformed all factors including histology, ICB type, and de novo BrM status in predicting icPFS (P = .030), LC (P = .042), and OS (P = .033). In the absence of corticosteroids, pre-SRS lymphocyte counts correlated with improved LC (P = .02). Radionecrosis was not associated with SRS-ICB interval, but with BrM size and number of ICB cycles received prior to SRS. CONCLUSION: Delivering SRS closer to ICB cycles was associated with improved icPFS, LC, and OS without affecting radionecrosis rates. This may present a therapeutic opportunity to improve BrM outcomes.
- Publisher
- Oxford Academic
- Keywords
- brain metastases; immunotherapy; neuro-oncology; stereotactic radiosurgery
- Research Division(s)
- Personalised Oncology
- PubMed ID
- 40718642
- Publisher's Version
- https://doi.org/10.1093/noajnl/vdaf130
- Open Access at Publisher's Site
https://doi.org/10.1093/noajnl/vdaf130- Terms of Use/Rights Notice
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Creation Date: 2025-08-08 03:14:12
Last Modified: 2025-08-08 03:14:30