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      TERT promoter mutation and its interaction with IDH mutations in glioma: Combined TERT promoter and IDH mutations stratifies lower-grade glioma into distinct survival subgroups-A meta-analysis of aggregate data.

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          Abstract

          The clinical significance of telomerase reverse transcriptase (TERT) promoter mutation in glioma remains unclear. The aim of our meta-analysis is to investigate the prognostic impact TERT promoter mutation in glioma patients and its interaction with other molecular markers, particularly Isocitrate Dehydrogenase (IDH) mutation from aggregate level data. Relevant articles were searched in four electronic databases including PubMed, Scopus, Web of Science and Virtual Health Library. Pooled HRs were calculated using random effect model weighted by inverse variance method. From 1010 studies, we finally included 28 studies with 11519 patients for meta-analyses. TERT mutation is significantly associated with compromised overall survival (OS) (HR=1.38; 95% CI=1.15-1.67) and progression-free survival (PFS) (HR=1.31; 95% CI=1.06-1.63) in glioma patients. In studying its reaction with IDH, TERT promoter mutation was associated with reduced OS in both IDH-mutant (IDH-mut) and IDH-wild type (IDH-wt) glioblastomas but shown to have inverse effects on IDH-mut and IDH-wt grade II/III tumors. Our analysis categorized WHO grade II/III glioma patients into four distinct survival subgroups with descending survival as follow: TERT-mut/IDH-mut≫TERT-wt/IDH-mut≫TERT-wt/IDH-wt≫TERT-mut/IDH-wt. Prognostic value of TERT promoter mutations in gliomas is dependent on tumor grade and the IDH mutational status. With the same tumor grade in WHO grade II and III tumors and the same IDH mutation status, TERT-mut is a prognostic factor.

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          Author and article information

          Journal
          Crit. Rev. Oncol. Hematol.
          Critical reviews in oncology/hematology
          Elsevier BV
          1879-0461
          1040-8428
          Dec 2017
          : 120
          Affiliations
          [1 ] Department of Pathology, Cho Ray Hospital, Ho Chi Minh City 70000, Viet Nam. Electronic address: huyvuong@hotmail.com.
          [2 ] Faculty of Medicine, University of Jordan, Amman, Jordan.
          [3 ] Pham Ngoc Thach University of Medicine, Ho Chi Minh City 70000, Viet Nam.
          [4 ] Department of Pathology, University of Medicine and Pharmacy at Ho Chi Minh City, Ho Chi Minh City 70000, Viet Nam; Faculty of Medicine, University of Medicine and Pharmacy at Ho Chi Minh City, Ho Chi Minh City 70000, Viet Nam.
          [5 ] Department of Pathology, Cho Ray Hospital, Ho Chi Minh City 70000, Viet Nam.
          [6 ] Department of Anatomical and Cellular Pathology, Chinese University of Hong Kong, Hong Kong, China.
          [7 ] Department of Neurosurgery, Seoul National University, College of Medicine, Seoul 110-744, Republic of Korea.
          [8 ] Department of Pathology, University of Oklahoma Health Sciences Center, Oklahoma City, OK 73104, United States.
          Article
          S1040-8428(17)30195-6
          10.1016/j.critrevonc.2017.09.013
          29198322
          1a3c41ac-ae88-4e5d-b5e5-9839a84a1cfd
          History

          Glioblastoma,TERT,Progression-free survival,Overall survival,Meta-analysis,IDH,Glioma

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