Evidence map›Paper›PMID 41693007›Full record

ArticleThe oncologist2026

Outcomes after SRS and ipilimumab plus nivolumab for melanoma brain metastases following prior immune checkpoint inhibitor or targeted therapy.

Ian Messing, Lauren Linkowski, Matthew D Riina, Melanie Berger, Jonathan Baron, Xingmei Wang, Michael Kallan, Harper G Hubbeling, Robert A Lustig, Jay F Dorsey and 14 more

Abstract read
In one paragraph

Article in The oncologist, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

24 authors.

Ian MessingDepartment of Radiation Oncology, University of Pennsylvania, Philadelphia, PA 19104, United States.ORCID 0000-0003-2950-9823
Lauren LinkowskiDepartment of Radiation Oncology, University of Pennsylvania, Philadelphia, PA 19104, United States.
Matthew D RiinaDepartment of Radiation Oncology, University of Pennsylvania, Philadelphia, PA 19104, United States.
Melanie BergerDepartment of Radiation Oncology, University of Pennsylvania, Philadelphia, PA 19104, United States.
Jonathan BaronDepartment of Radiation Oncology, University of Pennsylvania, Philadelphia, PA 19104, United States.
Xingmei WangDepartment of Radiation Oncology, University of Pennsylvania, Philadelphia, PA 19104, United States.
Michael KallanDepartment of Radiation Oncology, University of Pennsylvania, Philadelphia, PA 19104, United States.
Harper G HubbelingDepartment of Radiation Oncology, University of Pennsylvania, Philadelphia, PA 19104, United States.
Robert A LustigDepartment of Radiation Oncology, University of Pennsylvania, Philadelphia, PA 19104, United States.
Jay F DorseyDepartment of Radiation Oncology, University of Pennsylvania, Philadelphia, PA 19104, United States.
Goldie KurtzDepartment of Radiation Oncology, University of Pennsylvania, Philadelphia, PA 19104, United States.
Suneel NagdaDepartment of Radiation Oncology, University of Pennsylvania, Philadelphia, PA 19104, United States.
John N LukensDepartment of Radiation Oncology, University of Pennsylvania, Philadelphia, PA 19104, United States.
Ahron FlowersDepartment of Medicine, University of Pennsylvania, Philadelphia, PA 19104, United States.
John Y K LeeDepartment of Neurosurgery, University of Pennsylvania, Philadelphia, PA 19104, United States.
Nduka M AmankulorDepartment of Neurosurgery, University of Pennsylvania, Philadelphia, PA 19104, United States.
Christina JacksonDepartment of Neurosurgery, University of Pennsylvania, Philadelphia, PA 19104, United States.
Suyash MohanDepartment of Radiology, University of Pennsylvania, Philadelphia, PA 19104, United States.ORCID 0000-0002-4025-115X
Ravi K AmaravadiDepartment of Medicine, University of Pennsylvania, Philadelphia, PA 19104, United States.
Lynn M SchuchterDepartment of Medicine, University of Pennsylvania, Philadelphia, PA 19104, United States.
Alexander C HuangDepartment of Medicine, University of Pennsylvania, Philadelphia, PA 19104, United States.
Tara C MitchellDepartment of Medicine, University of Pennsylvania, Philadelphia, PA 19104, United States.
Michelle Alonso-BasantaDepartment of Radiation Oncology, University of Pennsylvania, Philadelphia, PA 19104, United States.
Emily S LebowDepartment of Radiation Oncology, University of Pennsylvania, Philadelphia, PA 19104, United States.ORCID 0000-0002-6614-0212

Funding

Role of progenitor exhausted CD8 T cells and the progenitor niche in anti-PD1 efficacyR01CA273018 · NCI · UNIVERSITY OF PENNSYLVANIA · PI HUANG, ALEXANDER · 2022 to 2025
$2.6M
NCI NIH HHS R01 CA273018
6 · The paper itself

Abstract

backgroundMelanoma brain metastases (BM) carry high morbidity and mortality despite advances in systemic therapy. Combined immune checkpoint inhibition (ICI) with ipilimumab and nivolumab (ipi/nivo) demonstrates intracranial activity, but the influence of prior systemic therapy exposure is poorly defined. This is the first real-world study evaluating outcomes of melanoma BM treated with stereotactic radiosurgery (SRS) and concurrent ipi/nivo, focusing on the impact of prior ICI or targeted therapy. PATIENTS AND

methodsWe retrospectively analyzed 68 patients with 413 melanoma BM treated with concurrent SRS and ipi/nivo from 2015 to 2025. Primary endpoints were overall survival (OS) and intracranial progression-free survival (iPFS). Secondary endpoints included local and distant control, radionecrosis, and leptomeningeal disease. Univariable and multivariable Cox models identified predictors of outcome.

resultsMedian OS was 24.0 months (12- and 24-month OS: 64% and 50%). ICI-naive patients had longer OS (50.5 vs. 17.6 months; P = 0.007) and iPFS (15.1 vs. 5.9 months) than those with prior ICI. On multivariable analysis, prior ICI (HR 2.23, 95% confidence interval [CI] 1.13-4.41), prior BRAF/MEKi (HR 2.26, 95% CI 1.01-5.04), and ≥11 SRS-treated lesions (HR 3.22, 95% CI 1.43-7.21) predicted worse outcomes, while higher graded prognostic assessment (GPA) favored OS (HR 0.46, 95% CI 0.29-0.75). At 24 months, local progression was 11%, distant 49%, radionecrosis 7%, and leptomeningeal disease 4%.

conclusionConcurrent SRS with ipi/nivo provides durable intracranial control with low toxicity. Patients with prior ICI or targeted therapy represent a high-risk subgroup with poorer outcomes, supporting exploration of intensified or novel strategies.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsBrain NeoplasmsImmune Checkpoint InhibitorsIpilimumabMelanomaNivolumabRadiosurgeryAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedRetrospective StudiesImmune Checkpoint InhibitorsIpilimumabNivolumabdual immune checkpoint inhibitionintracranial disease controlipilimumab and nivolumabmelanoma brain metastasesprior immune checkpoint inhibitor exposurestereotactic radiosurgery

Identifiers

PMID41693007
PMCPMC13010309

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.