Evidence map›Paper›PMID 37355350›Full record

ArticleAnais brasileiros de dermatologia

Tumoral inflammatory infiltrate does not predict metastases in thin primary cutaneous melanomas.

Mariele Bevilaqua, Maria Carolina Widholzer Rey, Gian Carlo Antonini Cappellini, Felice Riccardi, Cristina Fortes, Adriana Vial Roehe, Renan Rangel Bonamigo

Open access · goldAbstract read
In one paragraph

Article in Anais brasileiros de dermatologia. 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
0.5field-weighted citation impact, top 27% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

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

7 authors at 6 institutions in 2 countries.

Mariele BevilaquaDepartment of Dermatology, Universidade Federal de Ciências da Saúde de Porto Alegre, Porto Alegre, RS, Brazil; Universidade Luterana do Brasil, Canoas, RS, Brazil. Electronic address: dramarielebevilaqua@gmail.com.
Maria Carolina Widholzer ReyDepartment of Dermatology, Santa Casa de Misericórdia de Porto Alegre, Porto Alegre, RS, Brazil.
Gian Carlo Antonini CappelliniDepartment of Oncology, Hospital Sandro Pertini, Rome, Italy.
Felice RiccardiDepartment of Oncological Surgery, Hospital Santa Rita, Santa Casa de Misericórdia de Porto Alegre, Porto Alegre, RS, Brazil.
Cristina FortesDepartment of Epidemiology, Istituto Dermopatico dell'Immacolata, Rome, Italy.
Adriana Vial RoeheDepartment of Patology, Universidade Federal de Ciências da Saúde de Porto Alegre, Porto Alegre, RS, Brazil.
Renan Rangel BonamigoDepartment of Dermatology, Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brazil; Department of Oncological Surgery, Hospital Santa Rita, Santa Casa de Misericórdia de Porto Alegre, Porto Alegre, RS, Brazil.
Universidade Federal de Ciências da Saúde de Porto Alegre · BRIstituto Dermopatico dell'Immacolata · ITOspedale Sandro Pertini · ITSanta Casa de Misericórdia de Marília · BRSanta Casa Hospital · BRUniversidade Federal do Rio Grande do Sul · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn cutaneous melanomas in general, tumor inflammatory infiltrate (TII) can protect against distant metastases, but there is no consensus when only thin primary cutaneous melanomas (TPCM) are considered.

objectiveTo investigate the presence of TII in TPCM and the relationship between TII and the occurrence of metastases.

methodsCase-control study including 50 patients with TPCM, 22 metastatic (MC group) and 28 non-metastatic (NMC group). The presence of TII was evaluated and, if present, qualified as mild, moderate or marked.

resultsThe mean age was 50.7 years in the MC and 56.2 years in the NMC group (p = 0.234), and the male sex predominated in the MC group (63.6%). The average Breslow thickness was higher in the MC when compared to that observed in the NMC (respectively 0.8 vs. 0.6 mm, p = 0.012). The presence of ulceration occurred in 22.7% of the MC and 17.9% of the NMC (p = 0.732). TII was present in all 50 TPCM, being marked or moderate in 67.9% of the NMC and 54.5% in the MC group (p = 0.503). In the multivariate analysis, the presence of moderate and marked TII had an Odds Ratio (OR) of 0.57 (95% Confidence Interval [CI]: 0.18‒1.8) and adjusted OR of 0.68 (95% CI 0.13‒3.99). STUDY LIMITATIONS: Small sample size.

conclusionsTII was present in all TPCM (with and without metastases), and it was not possible to demonstrate a protective effect of TII against the appearance of metastases.

Indexed as

MelanomaSkin NeoplasmsCase-Control StudiesCutaneous Malignant MelanomaHumansMaleMiddle AgedPrognosisBiomarkersLymphocytes, tumor-infiltratingMelanomaNeoplasm metastasisPrognosis

Identifiers

PMID37355350
PMCPMC10589460
OpenAlexW4381684765

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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.