Evidence map›Paper›PMID 36230856›Full record

ArticleCancers2022

TERT Promoter and BRAF V600E Mutations in Papillary Thyroid Cancer: A Single-Institution Experience in Korea.

Min Jhi Kim, Jin Kyong Kim, Gi Jeong Kim, Sang-Wook Kang, Jandee Lee, Jong Ju Jeong, Woong Youn Chung, Daham Kim, Kee-Hyun Nam

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 9% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Guideline
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  12. BRAFCancers · 2023
    Article
  13. Younger Than 55 Years Old andInternational journal of general medicine · 2023
    Article
  14. 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

9 authors at 2 institutions in 1 country.

Min Jhi KimDepartment of Surgery, CHA Ilsan Medical Center, CHA University School of Medicine, Goyang-si 10414, Korea.ORCID 0000-0002-7791-2994
Jin Kyong KimDepartment of Surgery, Yonsei University College of Medicine, Seoul 03722, Korea.
Gi Jeong KimDepartment of Pathology, Yonsei University College of Medicine, Seoul 03722, Korea.
Sang-Wook KangDepartment of Surgery, Yonsei University College of Medicine, Seoul 03722, Korea.ORCID 0000-0001-5355-833X
Jandee LeeDepartment of Surgery, Yonsei University College of Medicine, Seoul 03722, Korea.ORCID 0000-0003-4090-0049
Jong Ju JeongDepartment of Surgery, Yonsei University College of Medicine, Seoul 03722, Korea.ORCID 0000-0002-4155-6035
Woong Youn ChungDepartment of Surgery, Yonsei University College of Medicine, Seoul 03722, Korea.
Daham KimDepartment of Internal Medicine, Institute of Endocrine Research, Yonsei University College of Medicine, Seoul 03722, Korea.ORCID 0000-0003-1871-686X
Kee-Hyun NamDepartment of Surgery, Yonsei University College of Medicine, Seoul 03722, Korea.
Yonsei University · KRCHA University · KR

Funding

The Basic Science Research Program through the National Research Foundation of Korea (NRF) 2021R1I1A1A01044993
6 · The paper itself

Abstract

Telomerase reverse transcriptase (TERT) promoter mutation has been investigated for its clinical and prognostic significance in aggressive papillary thyroid cancer (PTC). In this study, we aimed to assess the prevalence, clinicopathologic features, and treatment outcomes of TERT mutation-positive PTCs along with the common BRAF V600E mutation. We performed mutational analyses for BRAF and the TERT promoter in thyroid cancer patients who had undergone surgery at our institution since 2019. We reviewed and analyzed 7797 patients with PTC in this study. The prevalence of BRAF V600E and TERT promoter mutations was 84.0% and 1.1%, respectively. Multifocal gene mutations in bilateral PTCs were identified. TERT promoter mutations were associated with older age, larger tumor size, tumor multifocality, tumor variants, advanced stages, more adjuvant radioactive iodine treatment (RAI), higher stimulated serum thyroglobulin level before RAI, and more uptakes in the regions outside the surgical field on a post-RAI whole-body scan. The coexistence of BRAF V600E and TERT promoter mutations exacerbated all clinicopathologic characteristics. The frequency of TERT promoter mutations was the lowest in this study, compared to previous studies. TERT promoter mutations consistently correlated with aggressive PTCs, and the synergistic effect of both mutations was evident. Specific clinical settings in our institution and in Korea may have led to these distinctive results. Prospective multicenter studies with longer follow-up periods are required to establish valuable oncologic outcomes.

Indexed as

BRAF V600Emutational analysispapillary thyroid cancerTERT promoter

Identifiers

PMID36230856
PMCPMC9563418
OpenAlexW4303685343

What OpenQuestion holds

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LicenceCC BY
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.