Evidence map›Paper›PMID 42052498›Full record

ArticleFrontiers in oncology2026

Case Report: The role of BRAF mutation in adjuvant and neoadjuvant treatment of melanoma patients: what is the optimal approach?

Francesca Romana Di Pietro, Rosa Falcone, Sofia Verkhovskaia, Giulia Poti, Cristina Maria Failla, Maria Luigia Carbone, Maria Francesca Morelli, Albina Rita Zappalà, Roberto Morese, Zorika Christiana Di Rocco and 4 more

Abstract readCase Reports
In one paragraph

Article in Frontiers in oncology, 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

14 authors.

Francesca Romana Di PietroOncology and Dermato-oncology Department, Rome, Istituto Dermopatico dell'Immacolata (IDI)-Scientific Institute for Research, Hospitalization and Healthcare (IRCCS), Rome, Italy.
Rosa FalconeOncology and Dermato-oncology Department, Rome, Istituto Dermopatico dell'Immacolata (IDI)-Scientific Institute for Research, Hospitalization and Healthcare (IRCCS), Rome, Italy.
Sofia VerkhovskaiaOncology and Dermato-oncology Department, Rome, Istituto Dermopatico dell'Immacolata (IDI)-Scientific Institute for Research, Hospitalization and Healthcare (IRCCS), Rome, Italy.
Giulia PotiOncology and Dermato-oncology Department, Rome, Istituto Dermopatico dell'Immacolata (IDI)-Scientific Institute for Research, Hospitalization and Healthcare (IRCCS), Rome, Italy.
Cristina Maria FaillaExperimental Immunology Laboratory, Istituto Dermopatico dell'Immacolata (IDI)-Scientific Institute for Research, Hospitalization and Healthcare (IRCCS), Rome, Italy.
Maria Luigia CarboneClinical Trial Center, Istituto Dermopatico dell'Immacolata (IDI)-Scientific Institute for Research, Hospitalization and Healthcare (IRCCS), Rome, Italy.
Maria Francesca MorelliOncology and Dermato-oncology Department, Rome, Istituto Dermopatico dell'Immacolata (IDI)-Scientific Institute for Research, Hospitalization and Healthcare (IRCCS), Rome, Italy.
Albina Rita ZappalàOncology and Dermato-oncology Department, Rome, Istituto Dermopatico dell'Immacolata (IDI)-Scientific Institute for Research, Hospitalization and Healthcare (IRCCS), Rome, Italy.
Roberto MoreseOncology and Dermato-oncology Department, Rome, Istituto Dermopatico dell'Immacolata (IDI)-Scientific Institute for Research, Hospitalization and Healthcare (IRCCS), Rome, Italy.
Zorika Christiana Di RoccoOncology and Dermato-oncology Department, Rome, Istituto Dermopatico dell'Immacolata (IDI)-Scientific Institute for Research, Hospitalization and Healthcare (IRCCS), Rome, Italy.
Gabriele PiescoOncology and Dermato-oncology Department, Rome, Istituto Dermopatico dell'Immacolata (IDI)-Scientific Institute for Research, Hospitalization and Healthcare (IRCCS), Rome, Italy.
Paolo ChesiOncology and Dermato-oncology Department, Rome, Istituto Dermopatico dell'Immacolata (IDI)-Scientific Institute for Research, Hospitalization and Healthcare (IRCCS), Rome, Italy.
Paolo MarchettiScientific Direction, Istituto Dermopatico dell'Immacolata (IDI)-Scientific Institute for Research, Hospitalization and Healthcare (IRCCS), Rome, Italy.
Federica De GalitiisOncology and Dermato-oncology Department, Rome, Istituto Dermopatico dell'Immacolata (IDI)-Scientific Institute for Research, Hospitalization and Healthcare (IRCCS), Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: While the benefit of adjuvant therapy is well established in patients with stage IIIB Case presentation: We report the clinical case of a patient with cutaneous melanoma initially diagnosed as stage IIIA, harboring BRAF V600E mutation, who did not receive any adjuvant therapy and developed locoregional recurrence within one year from diagnosis. The patient was subsequently treated with anti-PD-1 neoadjuvant immunotherapy but experienced disease progression at both local and distant sites. Then, targeted therapy was initiated, leading to a rapid clinical and radiological improvement. Conclusion: Despite significant advances in the treatment of stage III melanoma, both in the adjuvant and, more recently, neoadjuvant settings, some patient subgroups require more tailored approaches. In particular, the presence of BRAF V600 mutation may indicate a more aggressive disease and identify patients who could benefit more from targeted therapy or combined immune checkpoint inhibition than from anti-PD-1 monotherapy.

Indexed as

adjuvant treatmentBRAF mutationIII stagemelanomaneoadjuvant strategy

Identifiers

PMID42052498
PMCPMC13110995

What OpenQuestion holds

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Registered trials

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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.