Evidence map›Paper›PMID 42053986›Full record

ArticleMelanoma research2026

Outcomes and prognostic factors in melanoma patients with leptomeningeal disease: a retrospective cohort study.

Mohamed A Aboelatta, Ali Rezazadeh, Ugur Sener, William G Breen, Riham Suleiman, Arkadiusz Z Dudek

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

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0citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Mohamed A AboelattaDepartment of Oncology.
Ali RezazadehDepartment of Oncology.
Ugur SenerDepartment of Neurology.
William G BreenDepartment of Radiation Oncology, Mayo Clinic, Rochester, Minnesota, USA.
Riham SuleimanDepartment of Oncology.
Arkadiusz Z DudekDepartment of Oncology.

Funding

Women's Cancer ProgramP30CA015083 · NCI · MAYO CLINIC ROCHESTER · PI Lila J. Rutten · 1985 to 2026
$151.3M
NCI NIH HHS P30 CA015083
6 · The paper itself

Abstract

Leptomeningeal disease (LMD) is a devastating complication of metastatic melanoma, affecting up to 15% of patients with central nervous system involvement. Despite advances in systemic therapy, LMD carries poor prognosis. Patients with LMD are often excluded from clinical trials. Contemporary real-world data on prognostic factors and treatment outcomes in melanoma LMD are limited. We conducted a retrospective cohort study of patients diagnosed with leptomeningeal metastasis from melanoma between 1 January 2018 and 31 December 2025, across Mayo Clinic sites. LMD diagnosis was made by magnetic resonance imaging showing leptomeningeal enhancement and confirmation from cerebrospinal fluid cytology and clinical presentation. Demographic, clinical, treatment, and outcome data were collected. Overall survival (OS) from LMD diagnosis was the primary endpoint. Forty-four patients were identified (median age: 60.0 years, range: 30.5-82.7). Before diagnosis of LMD, systemic therapy for metastatic disease was given to 91% of patients. BRAF mutations were present in 65.9%. After LMD diagnosis, 88.6% were treated for LMD. Median OS was 2.96 months (95% confidence interval: 1.39-4.53). Poor Eastern Cooperative Oncology Group performance status was independently associated with worse OS (hazard ratio: 2.10, P = 0.036). Any treatment for LMD (hazard ratio: 0.16, P = 0.005) was associated with improved OS. Melanoma-related LMD remains rapidly fatal. Studies of novel treatments are needed to improve outcomes for patients with this diagnosis.

Indexed as

MelanomaMeningeal NeoplasmsSkin NeoplasmsAdultAgedAged, 80 and overFemaleHumansMaleMiddle AgedPrognosisProto-Oncogene MasRetrospective StudiesMAS1 protein, humanProto-Oncogene Masimmune checkpoint inhibitorsmelanomameningeal carcinomatosismeningeal neoplasmsproto-Oncogene Proteins B-rafradiation

Identifiers

PMID42053986
PMCPMC13124253

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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.