Evidence map›Paper›PMID 33808846›Full record

ReviewJournal of clinical medicine2021

Oral Manifestations in Melanoma Patients Treated with Target or Immunomodulatory Therapies.

Emi Dika, Martina Lambertini, Bruna Gouveia, Martina Mussi, Emanuela Marcelli, Elena Campione, Carlotta Gurioli, Barbara Melotti, Aurora Alessandrini, Simone Ribero

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 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

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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

10 authors at 5 institutions in 2 countries.

Emi DikaDivision of Dermatology, IRCCS-Policlinico Sant'Orsola, via Massarenti 9, 40138 Bologna, Italy.ORCID 0000-0003-3186-2861
Martina LambertiniDivision of Dermatology, Department of Experimental, Diagnostic and Specialty Medicine (DIMES), University of Bologna, 40138 Bologna, Italy.ORCID 0000-0003-4282-342X
Bruna GouveiaThe Poche Centre, Melanoma Institute of Australia, 40 Rocklands Rd, Wollstonecraft, NSW 2065, Australia.
Martina MussiDivision of Dermatology, Department of Experimental, Diagnostic and Specialty Medicine (DIMES), University of Bologna, 40138 Bologna, Italy.ORCID 0000-0003-0955-6112
Emanuela MarcelliLaboratory of Bioengineering, Department of Experimental, Diagnostic and Specialty Medicine (DIMES), University of Bologna, 40138 Bologna, Italy.
Elena CampioneDermatology Unit, University of Rome Tor Vergata, 00133 Roma, Italy.
Carlotta GurioliDivision of Dermatology, IRCCS-Policlinico Sant'Orsola, via Massarenti 9, 40138 Bologna, Italy.
Barbara MelottiDivision of Dermatology, IRCCS-Policlinico Sant'Orsola, via Massarenti 9, 40138 Bologna, Italy.
Aurora AlessandriniDivision of Dermatology, IRCCS-Policlinico Sant'Orsola, via Massarenti 9, 40138 Bologna, Italy.
Simone RiberoDepartment of Medical Sciences, Dermatologic Clinic, University of Turin, 10126 Turin, Italy.
IRCCS Azienda Ospedliero-Universitaria di Bologna Policlinico di Sant'Orsola · ITUniversity of Bologna · ITMelanoma Institute Australia · AUUniversity of Rome Tor Vergata · ITUniversity of Turin · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBRAF (v-raf murine sarcoma viral oncogene homolog B1) and MEK (mitogen activated protein kinase) inhibitors, as well as immunotherapy against cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4) and the programmed cell death 1 (PD-1) receptor and its ligand (PD-L1), have shown good results in improving the disease-free survival of patients with metastatic melanoma (MM). The aim of this review is to summarize the main oral adverse events (oAEs) occurring in patients undergoing target or immunotherapy. We proposed two separate sections: oAEs during the treatment with (1) target therapies with BRAF and MEK inhibitors and tyrosine kinase inhibitors (gingival hyperplasia, pigmentation disorders, squamo-proliferative lesions) and (2) immunotherapies with CTLA-4 or PD1 inhibitors (lichenoid reactions, immuno-bullous reactions, xerostomia and other reactions). Adverse events frequently include oAEs, although these are often misdiagnosed and under-reported. Indeed, the oral cavity is not routinely evaluated during clinical practice. The symptomatology related to oAEs is significant since it may represent the first manifestation of a severe systemic reaction, possibly leading to difficulties in nutrition with a consequent impact on patients' quality of life. A careful examination of the oral cavity is recommended during the evaluation of oncologic patients in order to promptly detect the onset of new manifestations.

Indexed as

adverse eventimmunotherapymelanomaoraltarget

Identifiers

PMID33808846
PMCPMC8003791
OpenAlexW3136378479

What OpenQuestion holds

Textmetadata
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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.