# Outcomes of patients with melanoma brain metastases treated with ipilimumab and nivolumab with or without upfront comprehensive stereotactic radiosurgery

**Authors:** Troy J Kleber, Denái R Milton, Subhiksha Srinivasan, Bikash Panthi, Warren Floyd, Eric A Goethe, Michael A Davies, Hussein A Tawbi, Isabella C Glitza Oliva, Diana Kaya, Jing Li, Todd A Swanson, Subha Perni, Martin C Tom, Chenyang Wang, Sujit Prabhu, Jeffrey S Weinberg, Ian E McCutcheon, Caroline Chung, Sherise D Ferguson, Thomas H Beckham

PMC · DOI: 10.1093/noajnl/vdaf276 · Neuro-Oncology Advances · 2026-01-07

## TL;DR

This study compares outcomes of melanoma brain metastases patients treated with immunotherapy alone or with added stereotactic radiosurgery, finding radiosurgery improves brain control but not survival.

## Contribution

A retrospective analysis showing upfront stereotactic radiosurgery improves intracranial control without affecting survival in melanoma brain metastases treated with ipi/nivo.

## Key findings

- Upfront cSRS was associated with reduced intracranial progression (median 37.6 vs 5.5 months).
- No significant difference in overall survival between upfront cSRS and deferred groups.
- Upfront cSRS was more common in patients with larger, symptomatic metastases and fewer BRAF V600 mutations.

## Abstract

The efficacy of ipilimumab and nivolumab (ipi/nivo) for melanoma brain metastases (MBMs) has been previously reported, leading to uncertainty regarding the optimal role of comprehensive stereotactic radiosurgery (cSRS). We therefore conducted a single-institution retrospective study to compare outcomes of upfront versus deferred cSRS for MBM treated with ipi/nivo.

We identified patients who started ipi/nivo for newly diagnosed MBMs between 2018 and 2023, with or without upfront cSRS. Patients with >15 MBMs, leptomeningeal disease, or whole-brain radiotherapy at baseline were excluded. Outcomes were compared using multivariable regression and reported as adjusted hazard ratios (aHRs) with 95% CIs.

Of the 132 patients identified, 52.3% received upfront cSRS and 47.7% did not. Patients who received upfront cSRS had larger maximum MBMs (median 2.3 vs 0.7 cm; P < .001), more symptomatic MBMs (59.4% vs 11.1%; P < .001), higher rates of upfront craniotomy (47.8% vs 7.9%; P < .001), and fewer BRAF V600 mutations (34.8% vs 54.0%; P = .035). Upfront cSRS was not associated with longer overall survival (median 47.0 mo vs not reached; aHR = 1.01 [95% CI, 0.60-1.68]; P = .98) but was associated with reduced incidence of intracranial progression (median 37.6 vs 5.5 mo; aHR = 0.40 [95% CI, 0.25-0.64]; P < .001).

In this retrospective study, upfront cSRS was more often used in patients with higher-risk MBM and was associated with improved intracranial control, although no significant survival benefit was observed. These findings suggest that starting ipi/nivo alone may be reasonable for lower-risk MBM, but prospective studies are needed to guide optimal integration of cSRS.

## Linked entities

- **Genes:** BRAF (B-Raf proto-oncogene, serine/threonine kinase) [NCBI Gene 673]
- **Diseases:** melanoma (MONDO:0005105)

## Full-text entities

- **Genes:** BRAF (B-Raf proto-oncogene, serine/threonine kinase) [NCBI Gene 673] {aka B-RAF1, B-raf, BRAF-1, BRAF1, NS7, RAFB1}
- **Diseases:** MBMs (MESH:D001932), leptomeningeal disease (MESH:D008577)
- **Chemicals:** ipilimumab (MESH:D000074324), ipi/nivo (-), nivolumab (MESH:D000077594)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12883207/full.md

## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC12883207/full.md

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Source: https://tomesphere.com/paper/PMC12883207