Poor prognosis associated with TERT gene alterations in meningioma is independent of the WHO classification: an individual patient data meta-analysis

Publikation: Beitrag in FachzeitschriftÜbersichtsartikel (Review)BeigetragenBegutachtung

Beitragende

  • Christian Mirian - , Universität Kopenhagen (Autor:in)
  • Anne Katrine Duun-Henriksen - , Danish Cancer Society Research Center (Autor:in)
  • Tareq Juratli - , Klinik und Poliklinik für Neurochirurgie, Massachusetts General Hospital, Harvard Medical School (HMS), Universitätsklinikum Carl Gustav Carus Dresden (Autor:in)
  • Felix Sahm - , Deutsches Krebsforschungszentrum (DKFZ) (Autor:in)
  • Sabine Spiegl-Kreinecker - , Johannes Kepler University Linz (Autor:in)
  • Matthieu Peyre - , Institut du Cerveau et de la Moelle Epinière (Autor:in)
  • Annamaria Biczok - , Deutsches Krebsforschungszentrum (DKFZ) (Autor:in)
  • Jörg-Christian Tonn - , Deutsches Krebsforschungszentrum (DKFZ) (Autor:in)
  • Stéphane Goutagny - , Hopital Beaujon (Autor:in)
  • Luca Bertero - , University of Turin (Autor:in)
  • Andrea Daniela Maier - , Universität Kopenhagen (Autor:in)
  • Maria Møller Pedersen - , Universität Kopenhagen (Autor:in)
  • Ian Law - , Copenhagen University Hospitals (Autor:in)
  • Helle Broholm - , Copenhagen University Hospitals (Autor:in)
  • Daniel P Cahill - , Harvard Medical School (HMS) (Autor:in)
  • Priscilla Brastianos - , Massachusetts General Hospital (Autor:in)
  • Lars Poulsgaard - , Universität Kopenhagen (Autor:in)
  • Kåre Fugleholm - , Universität Kopenhagen (Autor:in)
  • Morten Ziebell - , Universität Kopenhagen (Autor:in)
  • Tina Munch - , Universität Kopenhagen (Autor:in)
  • Tiit Mathiesen - , Universität Kopenhagen (Autor:in)

Abstract

BACKGROUND: TERT gene alterations (TERT-alt) have been linked to increased risk of recurrence in meningiomas, whereas the association to mortality largely remain incompletely investigated. As incongruence between clinical course and WHO grade exists, reliable biomarkers have been sought.

METHODS: We applied the Preferred Reporting Items for Systematic Review and Meta-Analyses of individual participant data Statement. We compiled data from eight studies and allocated patients to TERT-alt (n=59) or TERT promoter wild-type (TERTp-wt; n=618). We compared the two groups stratified for WHO grades as: incidence rates, survival probabilities and cumulative recurrences. We estimated the effects of WHO grade, age at diagnosis and sex as HRs.

RESULTS: TERT-alt occurred in 4.7%, 7.9% and 15.4% of WHO-I/WHO-II/WHO-III meningiomas, respectively. The median recurrence-free survival was 14 months for all TERT-alt patients versus 101 months for all TERTp-wt patients. The HR for TERT-alt was 3.74 in reference to TERTp-wt. For all TERT-alt patients versus all TERTp-wt patients, the median overall survival was 58 months and 160 months, respectively. The HR for TERT-alt was 2.77 compared with TERTp-wt. TERT-alt affected prognosis independent of WHO grades. Particularly, the recurrence rate was 4.8 times higher in WHO-I/-II TERT-alt patients compared with WHO-III TERTp-wt patients. The mortality rate was 2.7 times higher in the WHO-I and WHO-II TERT-alt patients compared with WHO-III TERTp-wt patients.

CONCLUSIONS: TERT-alt is an important biomarker for significantly higher risk of recurrence and death in meningiomas. TERT-alt should be managed and surveilled aggressively. We propose that TERT-alt analysis should be implemented as a routine diagnostic test in meningioma and integrated into the WHO classification.

TRIAL REGISTRATION NUMBER: PROSPERO: CRD42018110566.

Details

OriginalspracheEnglisch
Seiten (von - bis)378-387
Seitenumfang10
FachzeitschriftJournal of Neurology, Neurosurgery and Psychiatry
Jahrgang91
Ausgabenummer4
PublikationsstatusVeröffentlicht - Apr. 2020
Peer-Review-StatusJa

Externe IDs

Scopus 85079739255

Schlagworte

Schlagwörter

  • Humans, Meningeal Neoplasms/genetics, Meningioma/genetics, Mutation, Prognosis, Promoter Regions, Genetic, Survival Rate, Telomerase/genetics, World Health Organization