Evidence map›Paper›PMID 33525348›Full record

ReviewJournal of clinical medicine2021

Cutaneous and Mucosal Melanomas of Uncommon Sites: Where Do We Stand Now?

Emi Dika, Martina Lambertini, Cristina Pellegrini, Giulia Veronesi, Barbara Melotti, Mattia Riefolo, Francesca Sperandi, Annalisa Patrizi, Costantino Ricci, Martina Mussi and 1 more

Open access · goldAbstract readReview
In one paragraph

Review in Journal of clinical medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.5field-weighted citation impact, top 15% of its field
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

17 citing papers in PubMed, 27 citations in OpenAlex.

  1. Review
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  12. Pigmented Oral Lesions: A Multicenter Study.European journal of dentistry · 2022
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  13. Review
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  15. Article
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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

11 authors at 4 institutions in 1 country.

Emi DikaDermatology, IRCCS Policlinico di Sant'Orsola, via Massarenti 9, 40138 Bologna, Italy.ORCID 0000-0003-3186-2861
Martina LambertiniDermatology, IRCCS Policlinico di Sant'Orsola, via Massarenti 9, 40138 Bologna, Italy.
Cristina PellegriniDermatology, Department of Biotechnological and Applied Clinical Science, University of L'Aquila, 67100 L'Aquila, Italy.
Giulia VeronesiDermatology, IRCCS Policlinico di Sant'Orsola, via Massarenti 9, 40138 Bologna, Italy.
Barbara MelottiDivision of Oncology, IRCCS di Policlinico Sant'Orsola, via Massarenti 9, 40138 Bologna, Italy.
Mattia RiefoloDepartment of Experimental, Diagnostic and Specialty Medicine, University of Bologna, 40138 Bologna, Italy.
Francesca SperandiDivision of Oncology, IRCCS di Policlinico Sant'Orsola, via Massarenti 9, 40138 Bologna, Italy.
Annalisa PatriziDermatology, IRCCS Policlinico di Sant'Orsola, via Massarenti 9, 40138 Bologna, Italy.ORCID 0000-0002-8398-0483
Costantino RicciDepartment of Experimental, Diagnostic and Specialty Medicine, University of Bologna, 40138 Bologna, Italy.ORCID 0000-0001-7254-4195
Martina MussiDermatology, IRCCS Policlinico di Sant'Orsola, via Massarenti 9, 40138 Bologna, Italy.ORCID 0000-0003-0955-6112
Maria Concetta FargnoliDermatology, Department of Biotechnological and Applied Clinical Science, University of L'Aquila, 67100 L'Aquila, Italy.ORCID 0000-0002-7249-2556
IRCCS Azienda Ospedliero-Universitaria di Bologna Policlinico di Sant'Orsola · ITUniversity of L'Aquila · ITFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico · ITUniversity of Bologna · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Melanomas arising at uncommon sites include a group of lesions related to unusual localizations in specific ethnic groups. The rarity of the disease often represents a limit to the participation of patients in specific trials. However, this peculiar genetic scenario has important therapeutic implications regarding new oncologic therapies. The aim of this article is to review the clinical features, somatic alterations and therapeutic options for melanomas of uncommon sites. They can be classified as cutaneous and mucosal lesions affecting the nail apparatus, palms/soles, oral mucosa, genital area and scalp. The prognosis may be worse compared to melanomas of other districts, and a prompt diagnosis may dramatically influence the outcome. Dermatologists and oncologists should therefore distinguish this melanoma subgroup in terms of surgical intervention and medical treatment. Due to the lack of mutations in genes usually found in cutaneous melanomas, the discovery of novel targets is required to develop new strategies and to change the prognosis of non-responders or wild-type patients.

Indexed as

acralgenitalmelanomanailoralscalp

Identifiers

PMID33525348
PMCPMC7866093
OpenAlexW3124574986

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.