Evidence map›Paper›PMID 26875008›Full record

ArticleInternational journal of cancer2016

TERT promoter mutations in melanoma survival.

Eduardo Nagore, Barbara Heidenreich, Sívaramakrishna Rachakonda, Zaida Garcia-Casado, Celia Requena, Virtudes Soriano, Christoph Frank, Victor Traves, Esther Quecedo, Josefa Sanjuan-Gimenez and 3 more

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in International journal of cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00341991 (Molecular Epidemiology of Cutaneous Malignant Melanoma), which is not on this map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed
8.7field-weighted citation impact, top 1% 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.

NCT00341991 completednot on this map

Molecular Epidemiology of Cutaneous Malignant Melanoma

TypeobservationalSponsorNational Cancer Institute (NCI)Ran2001 to 2020Enrolled15,401ConditionsMelanoma
3 · Its place in the literature

Who cites it

69 citing papers in PubMed, 120 citations in OpenAlex.

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  7. Utility and Micro-Costing Framework forDiagnostics (Basel, Switzerland) · 2024
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  11. Heliyon · 2023
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  14. Dermoscopic features associated with 3-GEP PLA: LINC00518, PRAME, and TERT expression in suspicious pigmented lesions.Skin research and technology : official journal of International Society for Bioengineering and the Skin (ISBS) [and] International Society for Digital Imaging of Skin (ISDIS) [and] International Society for Skin Imaging (ISSI) · 2023
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9 more citing papers are in PubMed but not listed here.

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

13 authors at 5 institutions in 4 countries.

Eduardo NagoreDepartment of Dermatology, Instituto Valenciano De Oncologia, Valencia, Spain.
Barbara HeidenreichDivision of Molecular Genetic Epidemiology, German Cancer Research Center, Heidelberg, Germany.
Sívaramakrishna RachakondaDivision of Molecular Genetic Epidemiology, German Cancer Research Center, Heidelberg, Germany.
Zaida Garcia-CasadoLaboratory of Molecular Biology, Instituto Valenciano De Oncologia, Valencia, Spain.
Celia RequenaDepartment of Dermatology, Instituto Valenciano De Oncologia, Valencia, Spain.
Virtudes SorianoMedical Oncology Department, Instituto Valenciano De Oncologia, Valencia, Spain.
Christoph FrankDivision of Molecular Genetic Epidemiology, German Cancer Research Center, Heidelberg, Germany.
Victor TravesDepartment of Pathology, Instituto Valenciano De Oncologia, Valencia, Spain.
Esther QuecedoDepartment of Dermatology, Hospital Arnau De Vilanova De Valencia, Valencia, Spain.
Josefa Sanjuan-GimenezDepartment of Pathology, Hospital Arnau De Vilanova De Valencia, Valencia, Spain.
Kari HemminkiDivision of Molecular Genetic Epidemiology, German Cancer Research Center, Heidelberg, Germany.
Maria Teresa LandiDivision of Epidemiology and Genetics, National Cancer Institute, US National Institutes of Health, Bethesda, MD.
Rajiv KumarDivision of Molecular Genetic Epidemiology, German Cancer Research Center, Heidelberg, Germany.
Fundación Instituto Valenciano de Oncología · ESGerman Cancer Research Center · DEHeidelberg University · DEHospital Arnau de Vilanova · ESDepartment of Health and Human Services · US

Funding

Family Studies ZIACP004410 · NCI · DIVISION OF CANCER EPIDEMIOLOGY AND GENETICS · PI SAVAGE, SHARON A. · 2009 to 2025
$56.1M
Intramural NIH HHS ZIA CP004410
6 · The paper itself

Abstract

Despite advances in targeted therapies, the treatment of advanced melanoma remains an exercise in disease management, hence a need for biomarkers for identification of at-risk primary melanoma patients. In this study, we aimed to assess the prognostic value of TERT promoter mutations in primary melanomas. Tumors from 300 patients with stage I/II melanoma were sequenced for TERT promoter and BRAF/NRAS mutations. Cumulative curves were drawn for patients with and without mutations with progression-free and melanoma-specific survival as outcomes. Cox proportional hazard regression models were used to determine the effect of the mutations on survivals. Individually, presence of TERT promoter and BRAF/NRAS mutations associated with poor disease-free and melanoma-specific survival with modification of the effect by the rs2853669 polymorphism within the TERT promoter. Hazard ratio (HR) for simultaneous occurrence of TERT promoter and BRAF/NRAS mutations for disease-free survival was 2.3 (95% CI 1.2-4.4) and for melanoma-specific survival 5.8 (95% CI 1.9-18.3). The effect of the mutations on melanoma-specific survival in noncarriers of variant allele of the polymorphism was significant (HR 4.5, 95% CI 1.4-15.2) but could not be calculated for the carriers due to low number of events. The variant allele per se showed association with increased survival (HR 0.3, 95% CI 0.1-0.9). The data in this study provide preliminary evidence that TERT promoter mutations in combination with BRAF/NRAS mutations can be used to identify patients at risk of aggressive disease and the possibility of refinement of the classification with inclusion of the rs2853669 polymorphism within TERT promoter.

Indexed as

PrognosisAdultAgedBiomarkers, TumorDisease-Free SurvivalGTP PhosphohydrolasesHumansKaplan-Meier EstimateMelanomaMembrane ProteinsMiddle AgedNeoplasm StagingPromoter Regions, GeneticProportional Hazards ModelsProto-Oncogene Proteins B-rafTelomeraseBiomarkers, TumorBRAF protein, humanGTP PhosphohydrolasesMembrane ProteinsNRAS protein, humanProto-Oncogene Proteins B-rafTelomeraseTERT protein, humanBRAF mutationsdisease-free survivalmelanomamelanoma-specific survivalTERT promoter mutations

Identifiers

PMID26875008
PMCPMC8238633
OpenAlexW2261233232

What OpenQuestion holds

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Registered trials

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.