Evidence map›Paper›PMID 39643819›Full record

ArticleArchives of dermatological research2024

Defining high-risk patients: beyond the 8the AJCC melanoma staging system.

Elisabetta Broseghini, Giulia Veronesi, Aldo Gardini, Federico Venturi, Biagio Scotti, Lorenzo Vespi, Paola Valeria Marchese, Barbara Melotti, Francesca Comito, Barbara Corti and 2 more

Abstract read
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In one paragraph

Article in Archives of dermatological research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Review
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  5. Review
  6. Article
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

12 authors.

Elisabetta Broseghini *IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, 40126, Italy.
Giulia Veronesi *Department of Medical and Surgical Science (DIMEC), University of Bologna, Bologna, 40138, Italy.
Aldo GardiniDepartment of Statistical Sciences, University of Bologna, Bologna, 40126, Italy.
Federico VenturiDepartment of Medical and Surgical Science (DIMEC), University of Bologna, Bologna, 40138, Italy. federico.venturi@hotmail.it.ORCID http://orcid.org/0000-0001-5053-4172
Biagio ScottiDepartment of Medical and Surgical Science (DIMEC), University of Bologna, Bologna, 40138, Italy.
Lorenzo VespiDepartment of Medical and Surgical Science (DIMEC), University of Bologna, Bologna, 40138, Italy.
Paola Valeria MarcheseOncology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, 40138, Italy.
Barbara MelottiOncology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, 40138, Italy.
Francesca ComitoOncology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, 40138, Italy.
Barbara CortiPathology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, 40138, Italy.
Manuela FerracinIRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, 40126, Italy.
Emi DikaDepartment of Medical and Surgical Science (DIMEC), University of Bologna, Bologna, 40138, Italy.ORCID http://orcid.org/0000-0003-3186-2861

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Since melanoma incidence is steadily increasing, guidelines regarding the diagnosis, staging, and treatment of melanoma are constantly being updated. In particular, the use of adjuvant therapy in stage IIb/c melanoma has been recently approved by the international regulatory agenicies. We performed a retrospective study with 92 melanoma patients namely 42 patients with IIb/c melanoma and 42 patients with IIIa stage melanoma, describing demographics, clinical, histology and disease course during the 5-year follow-up.Several significant evidences emerged between the two groups. Stage IIb/c patients possess a higher age of disease onset (69.6 vs. 55.5 years) with respect to stage III patients and the acral localization appeared as the most frequent (24% vs. 4%). Histologically, stage IIb/c melanomas more frequently exhibit ulceration (70% vs. 2%), angiotropism (54% vs. 8%) and are characterized by a greater presence of TILS (52% vs. 15%). Although it is not statistically significant, we observed a difference in terms of presence of metastasis during the 5-year follow-up: 15% of stage IIb/c patients showed metastasis vs. 4% of stage IIIa patients. Our data support the use of adiuvant immunotherapy in stage IIb/c patients.

Indexed as

MelanomaNeoplasm StagingSkin NeoplasmsAdultAgedAged, 80 and overFemaleFollow-Up StudiesHumansMaleMiddle AgedRetrospective Studies

Identifiers

PMID39643819

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.