Evidence map›Paper›PMID 30211730›Full record

ArticleThe American Journal of dermatopathology2019

Utility of TERT Promoter Mutations for Cutaneous Primary Melanoma Diagnosis.

Nancy E Thomas, Sharon N Edmiston, Yihsuan S Tsai, Joel S Parker, Paul B Googe, Klaus J Busam, Glynis A Scott, Daniel C Zedek, Eloise A Parrish, Honglin Hao and 6 more

Abstract read
In one paragraph

Article in The American Journal of dermatopathology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 12% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 44 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Utility and Micro-Costing Framework forDiagnostics (Basel, Switzerland) · 2024
    Article
  5. New Insights into Melanoma Tumor Syndromes.JID innovations : skin science from molecules to population health · 2022
    Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. TERT amplification but not activation of canonical Wnt/β-catenin pathway is involved in acral lentiginous melanoma progression to metastasis.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2020
    Article
  11. Review
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

16 authors at 4 institutions in 1 country.

Nancy E ThomasDepartment of Dermatology, School of Medicine, University of North Carolina, Chapel Hill, NC.
Sharon N EdmistonDepartment of Dermatology, School of Medicine, University of North Carolina, Chapel Hill, NC.
Yihsuan S TsaiLineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC.
Joel S ParkerLineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC.
Paul B GoogeDepartment of Dermatology, School of Medicine, University of North Carolina, Chapel Hill, NC.
Klaus J BusamDepartment of Pathology, Memorial Sloan-Kettering Cancer Center, Manhattan, NY.
Glynis A ScottDepartments of Dermatology, and.
Daniel C ZedekDepartment of Dermatology, School of Medicine, University of North Carolina, Chapel Hill, NC.
Eloise A ParrishLineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC.
Honglin HaoDepartment of Dermatology, School of Medicine, University of North Carolina, Chapel Hill, NC.
Nathaniel A SlaterDepartment of Dermatology, School of Medicine, University of North Carolina, Chapel Hill, NC.
Michelle V PearlsteinDepartment of Dermatology, School of Medicine, University of North Carolina, Chapel Hill, NC.
Jill S FrankLineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC.
Pei Fen KuanDepartment of Applied Mathematics and Statistics, State University of New York, Stony Brook, NY.
David W OllilaLineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC.
Kathleen ConwayDepartment of Dermatology, School of Medicine, University of North Carolina, Chapel Hill, NC.
University of North Carolina at Chapel Hill · USMemorial Sloan Kettering Cancer Center · USStony Brook University · USUniversity of Rochester · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
Virology Research Program (Program 4)P30CA016086 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Deborah F. Tate · 1985 to 2026
$201.5M
Sex Differences in Methylome Alterations and Mutational Burden in Early Stage MelanomaP01CA206980 · NCI · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI BERWICK, MARIANNE, THOMAS, NANCY E. · 2017 to 2022
$10.1M
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
High-Throughput DNA-Methylation Profiling from Fixed Melanocytic TissuesR33CA160138 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DORSEY, KATHLEEN CONWAY, THOMAS, NANCY E. · 2011 to 2013
$979k
DNA-Methylation Profiling from Fixed Melanocytic TissuesR21CA134368 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DORSEY, KATHLEEN CONWAY, THOMAS, NANCY E. · 2009 to 2010
$356k
TERT Promoter Mutation as a Melanoma BiomarkerR03CA199487 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI DORSEY, KATHLEEN CONWAY, THOMAS, NANCY E. · 2015 to 2016
$152k
NCI NIH HHS P01 CA206980NCI NIH HHS P30 CA008748NCI NIH HHS P30 CA016086NCI NIH HHS R01 CA233524NCI NIH HHS R03 CA199487NCI NIH HHS R21 CA134368NCI NIH HHS R33 CA160138
6 · The paper itself

Abstract

Telomerase reverse transcriptase (TERT) promoter mutations are commonly found in malignant melanomas but rare in melanocytic nevi. To assess its potential diagnostic utility for the distinction of melanoma from nevus, we determined the TERT promoter mutation status of 86 primary melanomas, 72 melanocytic nevi, and 40 diagnostically problematic melanocytic proliferations. Of the 86 melanomas, 67 (77.9%) were TERT-positive, defined as harboring a hotspot TERT promoter mutation at positions -124C>T, -124_125CC>TT, -138_139CC>TT, or -146C>T. Of the 72 nevi, only 1 (1.4%) was TERT-positive. Of the 40 diagnostically uncertain melanocytic proliferations, 2 (5.0%) were TERT-positive. TERT positivity as a test for melanoma versus nevus had an accuracy of 87.3% [95% confidence interval (CI), 81.1-92.1], a sensitivity of 77.9% (95% CI, 68.9-85.4), a specificity of 98.6% (95% CI, 95.8-100), a positive predictive value of 98.5% (95% CI, 95.6-100), and a negative predictive value of 78.9% (95% CI, 72.6-85.4). Our results indicate that hotspot TERT promoter mutation status may be a useful ancillary parameter for the diagnosis of melanoma. In particular, the high specificity of these mutations for melanoma indicates the presence of a TERT promoter mutation in a melanocytic neoplasm associated with diagnostic controversy, or uncertainty should increase concern for a melanoma.

Indexed as

AdultAgedCutaneous Malignant MelanomaFemaleHumansMaleMelanomaMiddle AgedMutationNevus, PigmentedPromoter Regions, GeneticSkin NeoplasmsTelomeraseTelomeraseTERT protein, human

Identifiers

PMID30211730
PMCPMC6411457
OpenAlexW2890414632

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

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.