Evidence map›Paper›PMID 39138770›Full record

ArticleAnnals of surgical oncology2024

Using Nomograms Wisely: Predicting Sentinel Node Positivity in Melanoma.

Priscila Rojas-Garcia, Bryan Ma, Eva Lindell Jonsson, Olivia Genereux, Gregory McKinnon, Thomas Brenn, Golpira Elmi Assadzadeh, Claire Temple-Oberle

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Article in Annals of surgical oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

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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

1 citing paper in PubMed.

  1. 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

8 authors.

Priscila Rojas-GarciaDepartment of Surgery, Tom Baker Cancer Centre, Calgary, AB, Canada.
Bryan MaDivision of Dermatology, Department of Medicine, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada.
Eva Lindell JonssonDepartment of Surgery, Tom Baker Cancer Centre, Calgary, AB, Canada.
Olivia GenereuxDepartment of Surgery, Tom Baker Cancer Centre, Calgary, AB, Canada.
Gregory McKinnonDepartment of Surgery, Tom Baker Cancer Centre, Calgary, AB, Canada.
Thomas BrennDepartment of Pathology and Laboratory Medicine, University of Calgary, Calgary, AB, Canada.
Golpira Elmi AssadzadehDepartment of Surgery, Tom Baker Cancer Centre, Calgary, AB, Canada.
Claire Temple-OberleDepartment of Surgery, Tom Baker Cancer Centre, Calgary, AB, Canada. claire.temple-oberle@albertahealthservices.ca.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFour externally validated sentinel node biopsy (SNB) prediction nomograms exist for malignant melanoma that each incorporate different clinical and histopathologic variables, which can result in substantially different risk estimations for the same patient. We demonstrate this variability by using hypothetical melanoma cases.

methodsWe compared the MSKCC and MIA calculators. Using a random number generator, 300 hypothetical thin melanoma "patients" were created with varying age, tumor thickness, Clark level, location on the body, ulceration, melanoma subtype, mitosis, and lymphovascular invasion (LVI). The chi-square test was used to detect statistically significant differences in risk estimations between nomograms. Multivariate linear regression was used to determine the most relevant contributing pathologic features in cases where the predictions diverged by > 10%.

resultsOf 300 randomly generated cases, 164 were deleted as their clinical scenarios were unlikely. The MSKCC nomogram generally calculated a lower risk than the MIA (p < 0.001). The highest risk score attained for any "patient" using MSKCC calculator was 15% achieved in one of 136 patients (0.7%), whereas using the MIA nomogram, 58 of 136 patients (43%, p < 0.001) had predicted risk >15%. Regression analysis on patients with >10% difference between nomograms revealed LVI (26, p < 0.001), mitosis (14, p < 0.001), and melanoma subtype (8, p < 0.001) were the factors with high coefficients within MIA that were not present in MSKCC.

conclusionsNomograms are useful tools when predicting SNB risk but provide risk outputs that are quite sensitive to included predictors.

Indexed as

MelanomaNomogramsSentinel Lymph NodeSentinel Lymph Node BiopsyAdultFemaleHumansLymphatic MetastasisMaleMiddle AgedNeoplasm InvasivenessPrognosisSkin NeoplasmsLymph node riskMlanomaNomogramsSentinel lymph node biopsyStage

Identifiers

PMID39138770

What OpenQuestion holds

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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.