Evidence map›Paper›PMID 39940799›Full record

ArticleInternational journal of molecular sciences2025

Recurrent Melanoma in a Patient with Chronic Lymphocytic Leukemia (CLL) Presenting with an Apparent Co-Existing NRAS and BRAF Mutation: A Diagnostic and Treatment Conundrum.

Giuliana G Berardi, Jabbar Muthanna, Y Lynn Wang, Anthony J Olszanski

Abstract readCase Reports
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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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

1 citing paper in PubMed.

  1. Article
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

4 authors.

Giuliana G BerardiDepartment of Medical Oncology, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.ORCID 0000-0001-5802-2008
Jabbar MuthannaDepartment of Pathology, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.
Y Lynn WangDepartment of Pathology, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.
Anthony J OlszanskiDepartment of Medical Oncology, Fox Chase Cancer Center, Philadelphia, PA 19111, USA.ORCID 0000-0001-5276-5898

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Melanoma is the fifth most common cancer in the United States. The advent of immunotherapy and molecular targeted therapy has improved progression-free and overall survival in many patients with advanced disease. However, the selection of therapeutic choices requires a nuanced approach, especially when considering molecularly targeted agents. This case report highlights a diagnostic and therapeutic challenge in managing a patient with a history of chronic lymphocytic leukemia (CLL) and recurrent melanoma. Molecular testing suggested discordant BRAF V600E testing and a simultaneous NRAS G12D mutation. After a careful literature review, repetition of his molecular testing, and analysis of the timelines and results of all his molecular testing, we concluded that the BRAF V600E mutation result was falsely positive. The patient was treated with two cycles of ipilimumab (1 mg/kg) and nivolumab (3 mg/kg) as per the NADINA trial and had a complete radiographic response. He then underwent resection demonstrating a pathologic partial response ranging from 20% to 95% tumor necrosis, dependent on the satellite examined. This case report underscores the importance of precise molecular diagnostics in guiding melanoma treatment and demonstrates the complexities of managing a patient with a coexisting malignancy.

Indexed as

GTP PhosphohydrolasesLeukemia, Lymphocytic, Chronic, B-CellMelanomaMembrane ProteinsMutationNeoplasm Recurrence, LocalProto-Oncogene Proteins B-rafHumansBRAF protein, humanGTP PhosphohydrolasesMembrane ProteinsNRAS protein, humanProto-Oncogene Proteins B-rafBRAF mutationchronic lymphocytic leukemiaNRAS mutationrecurrent melanoma

Identifiers

PMID39940799
PMCPMC11817975

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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.