Evidence map›Paper›PMID 35659273›Full record

ArticleBMC cancer2022

The role of sentinel node tumor burden in modeling the prognosis of melanoma patients with positive sentinel node biopsy: an Italian melanoma intergroup study (N = 2,086).

Saveria Tropea, Paolo Del Fiore, Andrea Maurichi, Roberto Patuzzo, Mario Santinami, Simone Ribero, Pietro Quaglino, Virginia Caliendo, Lorenzo Borgognoni, Serena Sestini and 12 more

Open access · goldAbstract read
In one paragraph

Article in BMC cancer, 2022. 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
0.8field-weighted citation impact, top 26% 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

6 citing papers in PubMed, 8 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

22 authors at 13 institutions in 1 country.

Saveria TropeaSoft-Tissue, Peritoneum and Melanoma Surgical Oncology Unit, Veneto Institute of Oncology IOV- IRCCS, 35128, Padua, Italy.
Paolo Del FioreSoft-Tissue, Peritoneum and Melanoma Surgical Oncology Unit, Veneto Institute of Oncology IOV- IRCCS, 35128, Padua, Italy. paolo.delfiore@iov.veneto.it.
Andrea MaurichiFondazione IRCCS Istituto Nazionale Dei Tumori, Melanoma and Sarcoma Unit, Milan, Italy.
Roberto PatuzzoFondazione IRCCS Istituto Nazionale Dei Tumori, Melanoma and Sarcoma Unit, Milan, Italy.
Mario SantinamiFondazione IRCCS Istituto Nazionale Dei Tumori, Melanoma and Sarcoma Unit, Milan, Italy.
Simone RiberoDepartment of Dermatologic Surgery, Città della Salute e della Scienza, Turin, Italy.
Pietro QuaglinoDepartment of Medical Sciences, Clinic of Dermatology, University of Turin, Turin, Italy.
Virginia CaliendoDermatologic Surgery Section, Oncologic Department, "Città Della Salute E Della Scienza Di Torino" University Hospital, Turin, Italy.
Lorenzo BorgognoniSOC Chirurgia Plastica Ricostruttiva E Melanoma & Skin Cancer Unit, Osp. SM Annunziata, AUSL Toscana Centro, Florence, Italy.
Serena SestiniSOC Chirurgia Plastica Ricostruttiva E Melanoma & Skin Cancer Unit, Osp. SM Annunziata, AUSL Toscana Centro, Florence, Italy.
Giuseppe GiudiceU.O.C. Di Chirurgia Plastica Ricostruttiva E Centro Ustioni Policlinico, University of Bari, Bari, Italy.
Eleonora NacchieroU.O.C. Di Chirurgia Plastica Ricostruttiva E Centro Ustioni Policlinico, University of Bari, Bari, Italy.
Corrado CaracòCorrado Caracò M.D., Struttura Complessa Chirurgia Oncologica Melanoma - Istituto Nazionale Tumori-Fondazione "G. Pascale", Naples, Italy.
Adriana CordovaDepartment- of Surgical Oncologic and Stomatologic Sciences, University of Palermo, Palermo, Italy.
Nicola SolariChirurgia Ospedaliera 1 Ospedale Policlinico San Martino, Genoa, Italy.
Dario PiazzalungaChirurgia Generale 1, Ospedale Papa Giovanni XXIII, Bergamo, Italy.
Francesca TauceriChirurgia E Terapie Oncologiche Avanzate Ospedale "GB.Morgagni-L.Pierantoni" - AUSL Forlì, Forlì, Italy.
Paolo CarcoforoUOC Chirurgia II Azienda Ospedaliera Universitaria Di Ferrara, Ferrara, Italy.
Maurizio LombardoDermatology Unit, Department of Specialistic Medicine, ASST Dei Sette Laghi, Varese, Italy.
Sara CavallariM.D. S. C. Chirurgia Generale ASST Carlo Poma, Mantua, Italy.
Simone MocellinSoft-Tissue, Peritoneum and Melanoma Surgical Oncology Unit, Veneto Institute of Oncology IOV- IRCCS, 35128, Padua, Italy.
Italian Melanoma Intergroup (IMI)
Fondazione IRCCS Istituto Nazionale dei Tumori · ITAzienda Usl Toscana Centro · ITIstituto Oncologico Veneto · ITUniversity of Bari Aldo Moro · ITUniversity of Turin · ITArcispedale Sant'Anna · ITAzienda Ospedaliera Carlo Poma · ITAzienda Ospedaliera Citta' della Salute e della Scienza di Torino · ITIstituto Nazionale Tumori IRCCS "Fondazione G. Pascale" · ITOspedale G.B. Morgagni - L.Pierantoni · ITOspedale Papa Giovanni XXIII · ITOspedale Policlinico San Martino · ITUniversity of Palermo · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe management of melanoma patients with metastatic melanoma in the sentinel nodes (SN) is evolving based on the results of trials questioning the impact of completion lymph node dissection (CLND) and demonstrating the efficacy of new adjuvant treatments. In this landscape, new prognostic tools for fine risk stratification are eagerly sought to optimize the therapeutic path of these patients.

methodsA retrospective cohort of 2,086 patients treated with CLND after a positive SN biopsy in thirteen Italian Melanoma Centers was reviewed. Overall survival (OS) was the outcome of interest; included independent variables were the following: age, gender, primary melanoma site, Breslow thickness, ulceration, sentinel node tumor burden (SNTB), number of positive SN, non-sentinel lymph nodes (NSN) status. Univariate and multivariate survival analyses were performed using the Cox proportional hazard regression model.

resultsThe 3-year, 5-year and 10-year OS rates were 79%, 70% and 54%, respectively. At univariate analysis, all variables, except for primary melanoma body site, were found to be statistically significant prognostic factors. Multivariate Cox regression analysis indicated that older age (P < 0.0001), male gender (P = 0.04), increasing Breslow thickness (P < 0.0001), presence of ulceration (P = 0.004), SNTB size (P < 0.0001) and metastatic NSN (P < 0.0001) were independent negative predictors of OS.

conclusionThe above results were utilized to build a nomogram in order to ease the practical implementation of our prognostic model, which might improve treatment personalization.

Indexed as

LymphadenopathyMelanomaSentinel Lymph NodeSkin NeoplasmsHumansLymphatic MetastasisLymph Node ExcisionMalePrognosisRetrospective StudiesSentinel Lymph Node BiopsyTumor BurdenCLNDCompletion lymph node dissectionMelanomaMetastatic melanoma in the sentinel nodesNomogramOverall survivalPrognostic factorsRisk stratificationTreatment of cutaneous melanomaTumor burden

Identifiers

PMID35659273
PMCPMC9166524
OpenAlexW4282024761

What OpenQuestion holds

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LicenceCC BY
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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.