Evidence map›Paper›PMID 25081751›Full record

ArticleModern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc2015

TERT promoter mutations contribute to subset prognostication of lower-grade gliomas.

Aden Ka-Yin Chan, Yu Yao, Zhenyu Zhang, Nellie Yuk-Fei Chung, Joseph Shu-Ming Liu, Kay Ka-Wai Li, Zhifeng Shi, Danny Tat-Ming Chan, Wai Sang Poon, Liangfu Zhou and 1 more

2 registry-linked trialsOpen access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 75 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed, 3 pooled it
5.6field-weighted citation impact, top 3% 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.

NCT02698280 phase2completednot on this map

Phase II Study of Bevacizumab and Nimustine in Patients With Recurrent High Grade Glioma

TypeinterventionalSponsorHuashan HospitalRan2015 to 2018Enrolled23ConditionsGlioblastomaArmsBevacizumab, Nimustine
NCT02766270 early_phase1unknown statusnot on this mapstarted 2016, after this paper: background citation

A Prospective Study of Concurrent Chemoradiotherapy With Temozolomide Versus Radiation Therapy Alone in Patients With IDH Wild-type/TERT Promoter Mutation Grade II/III Gliomas

TypeinterventionalSponsorBeijing Tiantan HospitalRan2016 to 2018Enrolled30ConditionsGrade II/III GliomaArmsTemozolomide, Radiotherapy
3 · Its place in the literature

Who cites it

75 citing papers in PubMed, 3 syntheses or guidelines pooled it, 116 citations in OpenAlex.

  1. Molecular Biomarker Testing for the Diagnosis of Diffuse Gliomas.Archives of pathology & laboratory medicine · 2022
    Guideline
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Article
  6. Article
  7. Review
  8. Article
  9. Prediction ofFrontiers in neurology · 2024
    Article
  10. Article
  11. Review
  12. Association of human telomerase reverse transcriptase promoter mutation with unfavorable prognosis in glioma: A systematic review and meta-analysis.Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences · 2023
    Review
  13. Article
  14. Molecular landscape of pediatric type IDH wildtype, H3 wildtype hemispheric glioblastomas.Laboratory investigation; a journal of technical methods and pathology · 2022
    Article
  15. Telomerase gene therapy: a remission toward cancer.Medical oncology (Northwood, London, England) · 2022
    Review
  16. Detection ofBiomedicines · 2022
    Review
  17. Article
  18. Review
  19. Article
  20. A Qualitative Signature to IdentifyFrontiers in molecular biosciences · 2022
    Article

15 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

11 authors at 4 institutions in 1 country.

Aden Ka-Yin Chan1] Department of Anatomical and Cellular Pathology, The Chinese University of Hong Kong, Hong Kong, China [2] The Chinese University of Hong Kong-Shenzhen Research Institute, Shenzhen, China.
Yu YaoDepartment of Neurosurgery, Huashan Hospital, Fudan University, Shanghai, China.
Zhenyu ZhangDepartment of Neurosurgery, Huashan Hospital, Fudan University, Shanghai, China.
Nellie Yuk-Fei Chung1] Department of Anatomical and Cellular Pathology, The Chinese University of Hong Kong, Hong Kong, China [2] The Chinese University of Hong Kong-Shenzhen Research Institute, Shenzhen, China.
Joseph Shu-Ming Liu1] Department of Anatomical and Cellular Pathology, The Chinese University of Hong Kong, Hong Kong, China [2] The Chinese University of Hong Kong-Shenzhen Research Institute, Shenzhen, China.
Kay Ka-Wai Li1] Department of Anatomical and Cellular Pathology, The Chinese University of Hong Kong, Hong Kong, China [2] The Chinese University of Hong Kong-Shenzhen Research Institute, Shenzhen, China.
Zhifeng ShiDepartment of Neurosurgery, Huashan Hospital, Fudan University, Shanghai, China.
Danny Tat-Ming ChanNeurosurgery Division, Department of Surgery, The Chinese University of Hong Kong, Hong Kong, China.
Wai Sang PoonNeurosurgery Division, Department of Surgery, The Chinese University of Hong Kong, Hong Kong, China.
Liangfu ZhouDepartment of Neurosurgery, Huashan Hospital, Fudan University, Shanghai, China.
Ho-Keung Ng1] Department of Anatomical and Cellular Pathology, The Chinese University of Hong Kong, Hong Kong, China [2] The Chinese University of Hong Kong-Shenzhen Research Institute, Shenzhen, China.
Chinese University of Hong Kong · CNChinese University of Hong Kong, Shenzhen · CNHuashan Hospital · CNFudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recurrent mutations in the promoter region of telomerase reverse transcriptase (TERT) have been found in various cancers including diffuse gliomas. Mutations lead to TERT upregulation and are associated with aggressive clinical behavior in glioblastomas. However, the clinical significance of TERT promoter mutations in lower-grade gliomas remains undetermined. The aim of this study is to evaluate the status of TERT promoter and the respective prognostic significance in a cohort of 237 lower-grade gliomas comprising grades II and III astrocytomas, oligodendrogliomas, and oligoastrocytomas. Mutually exclusive mutations in TERT promoter, C228T and C250T, were identified in 16/105 (15%) diffuse astrocytomas, 16/63 (25%) anaplastic astrocytomas, 13/18 (72%) oligodendrogliomas, 3/3 (100%) anaplastic oligodendrogliomas, 17/45 (38%) oligoastrocytomas, and 2/3 (67%) anaplastic oligoastrocytomas. Mutations co-occurred with 1p/19q codeletion (P<0.001) and are associated with oligodendroglial histology (P<0.001). Kaplan-Meier's survival analysis showed that TERT promoter mutation (P=0.037), Isocitrate dehydrogenase (IDH) mutation (P<0.001), and 1p/19q codeletion (P<0.001) were associated with favorable overall survival (OS). In the subset of 116 IDH-mutated lower-grade gliomas lacking 1p/19q codeletion, 19 TERT promoter-mutated tumors exhibited longer progression-free survival (PFS) (P=0.027) and OS (P=0.004). Consistent with this observation, in the subset of 97 IDH-mutated astrocytomas, 14 TERT promoter-mutated tumors showed longer PFS (P=0.001) and OS (P=0.001). In contrast, among the subset of 74 IDH wild-type lower-grade gliomas with intact 1p/19q, TERT promoter mutation was associated with shorter PFS (P=0.001) and OS (P=0.001). Similarly, in the subset of 65 IDH wild-type astrocytomas, 16 TERT promoter-mutated tumors exhibited unfavorable PFS (P=0.007) and OS (P=0.008). Our results indicate that when combined with IDH status, TERT promoter mutation contributes to prognostic subgroups of lower-grade astrocytic tumors or 1p/19q intact lower-grade gliomas and this may further refine future molecular classification of lower-grade gliomas.

Indexed as

Promoter Regions, GeneticAdultBrain NeoplasmsDisease-Free SurvivalDNA Mutational AnalysisFemaleGliomaHumansIn Situ Hybridization, FluorescenceKaplan-Meier EstimateMaleMiddle AgedNeoplasm GradingPrognosisProportional Hazards ModelsTelomeraseTelomeraseTERT protein, human

Identifiers

PMID25081751
OpenAlexW2079949890

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.