Evidence map›Paper›PMID 30181807›Full record

ArticleOncotarget2018

Metastases risk in thin cutaneous melanoma: prognostic value of clinical-pathologic characteristics and mutation profile.

Antonio G Richetta, Virginia Valentini, Federica Marraffa, Giovanni Paolino, Piera Rizzolo, Valentina Silvestri, Veronica Zelli, Anna Carbone, Cinzia Di Mattia, Stefano Calvieri and 3 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.4field-weighted citation impact, top 34% 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

13 citing papers in PubMed, 20 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

13 authors at 2 institutions in 1 country.

Antonio G RichettaDepartment of Internal Medicine and Medical Specialties, Unit of Dermatology, "Sapienza" University of Rome, Rome, Italy.
Virginia ValentiniDepartment of Molecular Medicine, "Sapienza" University of Rome, Rome, Italy.
Federica MarraffaDepartment of Internal Medicine and Medical Specialties, Unit of Dermatology, "Sapienza" University of Rome, Rome, Italy.
Giovanni PaolinoDepartment of Internal Medicine and Medical Specialties, Unit of Dermatology, "Sapienza" University of Rome, Rome, Italy.
Piera RizzoloDepartment of Molecular Medicine, "Sapienza" University of Rome, Rome, Italy.
Valentina SilvestriDepartment of Molecular Medicine, "Sapienza" University of Rome, Rome, Italy.
Veronica ZelliDepartment of Molecular Medicine, "Sapienza" University of Rome, Rome, Italy.
Anna CarboneDepartment of Oncological and Preventative Dermatological, San Gallicano Dermatological Institute, IRCCS, Rome, Italy.
Cinzia Di MattiaLaboratory of Cutaneous Histopathology, San Gallicano Dermatologic Institute, Rome, Italy.
Stefano CalvieriDepartment of Internal Medicine and Medical Specialties, Unit of Dermatology, "Sapienza" University of Rome, Rome, Italy.
Pasquale FrascioneDepartment of Oncological and Preventative Dermatological, San Gallicano Dermatological Institute, IRCCS, Rome, Italy.
Pietro DonatiLaboratory of Cutaneous Histopathology, San Gallicano Dermatologic Institute, Rome, Italy.
Laura OttiniDepartment of Molecular Medicine, "Sapienza" University of Rome, Rome, Italy.
Sapienza University of Rome · ITSan Gallicano Hospital · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundA high percentage of patients with thin melanoma (TM), defined as lesions with Breslow thickness ≤1 mm, presents excellent long-term survival, however, some patients develop metastases. Existing prognostic factors cannot reliably differentiate TM patients at risk for metastases.

objectiveWe aimed at characterizing the clinical-pathologic and mutation profile of metastatic and not-metastatic TM in order to distinguish lesions at risk of metastases.

methodsClinical-pathologic characteristics were recorded for the TM cases analyzed. We used a Next Generation Sequencing (NGS) multi-gene panel to characterize TM for multiple somatic mutations.

resultsA statistically significant association emerged between the presence of metastases and Breslow thickness ≥0.6 mm (

conclusionOur study indicates Breslow thickness ≥0.6 mm as a valid prognostic factor to distinguish TM at risk for metastases.

Indexed as

Breslow thicknessmetastasesmutation profileprognostic factorsthin melanoma

Identifiers

PMID30181807
PMCPMC6114949
OpenAlexW2886276266

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.