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Updated: Feb 5, 2026

Stereotactic Radiosurgery for Gynecologic Cancer
Published on: April 17, 2012
Robotic Stereotactic Radiosurgery in Melanoma Patients with Brain Metastases under Simultaneous Anti-PD-1 Treatment
Maike Trommer-Nestler1,2,3, Simone Marnitz4,5,6, Martin Kocher7,8,9
1Department of Radiation Oncology and Cyberknife Center, University Hospital of Cologne, Kerpener Str. 62, 50937 Cologne, Germany. maike.trommer-nestler@uk-koeln.de.
Abstract:
Combination concepts of radiotherapy and immune checkpoint inhibition are currently of high interest. We examined imaging findings, acute toxicity, and local control in patients with melanoma brain metastases receiving programmed death 1 (PD-1) inhibitors and/or robotic stereotactic radiosurgery (SRS). Twenty-six patients treated with SRS alone (n = 13; 20 lesions) or in combination with anti-PD-1 therapy (n = 13; 28 lesions) were analyzed. Lesion size was evaluated three and six months after SRS using a volumetric assessment based on cranial magnetic resonance imaging (cMRI) and acute toxicity after 12 weeks according to the Common Terminology Criteria for Adverse Events (CTCAE). Local control after six months was comparable (86%, SRS + anti-PD-1, and 80%, SRS). All toxicities reported were less than or equal to grade 2. One metastasis (5%) in the SRS group and six (21%) in the SRS + anti-PD-1 group increased after three months, whereas four (14%) of the six regressed during further follow-ups. This was rated as pseudoprogression (PsP). Three patients (23%) in the SRS + anti-PD-1 group showed characteristics of PsP. Treatment with SRS and anti-PD-1 antibodies can be combined safely in melanoma patients with cerebral metastases. Early volumetric progression of lesions under simultaneous treatment may be related to PsP; thus, the evaluation of combined radioimmunotherapy remains challenging and requires experienced teams.
Insights
Combining stereotactic radiosurgery (SRS) with programmed death 1 (PD-1) inhibitors is safe for melanoma brain metastases. Early lesion growth may indicate pseudoprogression, requiring careful evaluation of combined radioimmunotherapy.
Area of Science:
- Oncology
- Radiology
- Immunotherapy
Background:
- Combination therapy of radiotherapy and immune checkpoint inhibition is gaining interest.
- Melanoma brain metastases present a significant clinical challenge.
Purpose of the Study:
- To evaluate imaging findings, acute toxicity, and local control in melanoma patients with brain metastases treated with stereotactic radiosurgery (SRS) alone or combined with anti-programmed death 1 (PD-1) therapy.
- To assess the safety and efficacy of combined radioimmunotherapy.
Main Methods:
- Retrospective analysis of 26 patients with melanoma brain metastases treated with SRS alone (n=13) or SRS + anti-PD-1 therapy (n=13).
- Volumetric assessment of lesion size using cranial magnetic resonance imaging (cMRI) at 3 and 6 months post-SRS.
- Toxicity assessment using Common Terminology Criteria for Adverse Events (CTCAE) up to 12 weeks.
Main Results:
- Local control at 6 months was comparable: 80% for SRS alone and 86% for SRS + anti-PD-1 therapy.
- All reported toxicities were grade 2 or less, indicating a safe toxicity profile.
- Pseudoprogression (PsP) was observed in 23% of patients receiving SRS + anti-PD-1 therapy, characterized by initial lesion increase followed by regression.
Conclusions:
- Stereotactic radiosurgery (SRS) can be safely combined with anti-programmed death 1 (PD-1) antibodies in melanoma patients with cerebral metastases.
- Early volumetric progression in combined treatment may represent pseudoprogression (PsP), complicating treatment evaluation.
- Combined radioimmunotherapy for melanoma brain metastases requires experienced teams for optimal assessment and management.
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