Evidence map›Paper›PMID 29462090›Full record

ArticleThe American journal of surgical pathology2018

Breslow Density Is a Novel Prognostic Feature That Adds Value to Melanoma Staging.

Gerald Saldanha, Jeremy Yarrow, Jay Pancholi, Katarina Flatman, Kah Wee Teo, Somaia Elsheik, Rebecca Harrison, Marie O'Riordan, Mark Bamford

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In one paragraph

Article in The American journal of surgical pathology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
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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

9 authors.

Gerald SaldanhaLeicester Cancer Research Centre, University of Leicester.
Jeremy YarrowLeicester Cancer Research Centre, University of Leicester.
Jay PancholiLeicester Cancer Research Centre, University of Leicester.
Katarina FlatmanLeicester Cancer Research Centre, University of Leicester.
Kah Wee TeoLeicester Cancer Research Centre, University of Leicester.
Somaia ElsheikDepartment of Cellular Pathology, Nottingham University Hospitals, Nottingham, UK.
Rebecca HarrisonDepartment of Cellular Pathology, University Hospitals of Leicester NHS Trust, Leicester.
Marie O'RiordanDepartment of Cellular Pathology, University Hospitals of Leicester NHS Trust, Leicester.
Mark BamfordDepartment of Cellular Pathology, University Hospitals of Leicester NHS Trust, Leicester.

Funding

Cancer Research UK 18370Cancer Research UK A18370
6 · The paper itself

Abstract

Histomorphologic prognostic biomarkers that can be measured using only an hematoxylin and eosin stain are very attractive because they are simple and cheap. We conceived an entirely novel biomarker of this type, the Breslow density (BD), which measures invasive melanoma cell density at the site where Breslow thickness (BT) is measured. This study assessed BD's prognostic value. In this study, BD was measured in 1329 melanoma patients. Measurement accuracy and precision was assessed using intraclass correlation coefficient (ICC). Survival was assessed with a primary end-point of melanoma-specific survival (MSS) and also overall survival and metastasis-free survival. We found that BD measurement was accurate compared with gold standard image analysis (ICC, 0.84). Precision was excellent for 3 observers with different experience (ICC, 0.93) and for an observer using only written instructions (ICC, 0.93). BD was a highly significant predictor in multivariable analysis for overall survival, MSS, and metastasis-free survival (each, P<0.001) and it explained MSS better than BT, but BT and BD together had best explanatory capability. A BD cut point of ≥65% was trained in 970 melanomas and validated in 359. This cut point showed promise as a novel way to upstage melanoma from T stage "a" to "b." BD was combined with BT to create a targeted burden score. This was a validated as an adjunct to American Joint Committee on Cancer stage. In summary, BD can be measured accurately and precisely. It demonstrated independent prognostic value and explained MSS better than BT alone. Notably, we demonstrated ways that BD could be used with American Joint Committee on Cancer version 8 staging.

Indexed as

AdultAgedFemaleHumansMaleMelanomaMiddle AgedNeoplasm InvasivenessNeoplasm StagingObserver VariationPredictive Value of TestsProgression-Free SurvivalReproducibility of ResultsRisk AssessmentRisk FactorsSkin Neoplasms

Identifiers

PMID29462090
PMCPMC6176905

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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.