Evidence map›Paper›PMID 41527214›Full record

ArticleThe American journal of surgical pathology2026

Prognostic Value of a Novel Nuclear Grading of Cutaneous Melanoma: The UNC Chapel Hill Method.

Sarah G McAlpine, Shantanu Srivatsa, Paige C Jones, Danielle Davari, Vivian Lei, Maria Melendez-Gonzalez, Kathryn Conlon, Mahlet Gebrekidan, Stergios J Moschos, Frances A Collichio and 7 more

Abstract read
In one paragraph

Article in The American journal of surgical pathology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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.

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

17 authors.

Sarah G McAlpineUniversity of North Carolina at Chapel Hill.
Shantanu SrivatsaUniversity of North Carolina at Chapel Hill.
Paige C JonesDepartment of Surgery, Division of Surgical Oncology.
Danielle DavariDepartment of Dermatology.
Vivian LeiDepartment of Dermatology.
Maria Melendez-GonzalezDepartment of Dermatology.
Kathryn ConlonDepartment of Surgery, Division of Surgical Oncology.
Mahlet GebrekidanDepartment of Surgery, Division of Surgical Oncology.
Stergios J MoschosDepartment of Medicine, Division of Oncology, University of North Carolina at Chapel Hill, School of Medicine, Chapel Hill, NC.
Frances A CollichioDepartment of Medicine, Division of Oncology, University of North Carolina at Chapel Hill, School of Medicine, Chapel Hill, NC.
Jonathan SorahDepartment of Medicine, Division of Oncology, University of North Carolina at Chapel Hill, School of Medicine, Chapel Hill, NC.
Sharon N EdmistonDepartment of Dermatology.
Kathleen ConwayDepartment of Dermatology.
Jayson MiedemaDepartment of Dermatology.
David W OllilaDepartment of Surgery, Division of Surgical Oncology.
Nancy E ThomasDepartment of Dermatology.
Paul B GoogeDepartment of Dermatology.

Funding

Cardiovascular Epidemiology Training GrantT32HL007055 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Wayne D. Rosamond · 1986 to 2026
$10.0M
Identification of Lethal Melanomas at the Time of DiagnosisR01CA233524 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI ANTON-CULVER, HODA A, BEGG, COLIN B · 2020 to 2024
$4.5M
NCI NIH HHS R01 CA233524NHLBI NIH HHS T32 HL007055
6 · The paper itself

Abstract

We developed a nuclear grading system for melanoma, the UNC Chapel Hill Method, akin to McGovern's 1970 classification, to evaluate its correlation with disease progression and adverse histologic features, including thickness, mitotic rate, and ulceration. This retrospective study analyzed 544 melanomas diagnosed from 2020 to 2023, with a median follow-up of 411 days; 89 patients experienced progression, and 22 died of disease. A dermatopathologist assigned nuclear grades based on nuclear size, membrane contour, nucleolar features, and chromatin arrangement. Grade 1 resembled nevus nuclei, Grade 3 exhibited marked nuclear abnormalities, and Grade 2 was intermediate. Kaplan-Meier survival analysis demonstrated significantly worse progression-free survival for Grade 3 lesions compared with grades 1 and 2 (P<0.003). Statistical analyses (Student t test, χ2, and Kruskal-Wallis) revealed that grade 3 melanomas were associated with increased age, Breslow thickness, mitotic rate, ulceration, advanced AJCC stage, and mortality (each P<0.05). In a univariate Cox model, grade 2 (HR: 1.7; 95% CI: 0.7-4.0) and grade 3 (HR: 3.6; 95% CI: 1.5-8.4) lesions had an increased risk of progression relative to grade 1. After adjusting for covariates, hazard ratios were attenuated for grade 2 (HR: 1.2; 95% CI: 0.5-2.9) and grade 3 (HR: 1.7; 95% CI: 0.7-4.2). These findings show nuclear grade is associated with melanoma progression, but increased statistical power with longer follow-up and additional cases are needed to assess its independent prognostic value.

Indexed as

Cell NucleusMelanomaNeoplasm GradingSkin NeoplasmsAdultAgedAged, 80 and overCutaneous Malignant MelanomaDisease ProgressionFemaleHumansMaleMiddle AgedPredictive Value of TestsPrognosisProgression-Free Survivalmelanocytesmelanomanuclear changespathologyprognosis

Identifiers

PMID41527214
PMCPMC13011903

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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.