Epidemiology and survival of adult-type diffuse glioma in Belgium during the molecular era

Author:

Pinson Harry1ORCID,Silversmit Geert2,Vanhauwaert Dimitri3,Vanschoenbeek Katrijn2,Okito Jean-Pierre Kalala1,De Vleeschouwer Steven45,Boterberg Tom6,De Gendt Cindy2

Affiliation:

1. Department of Neurosurgery, Ghent University Hospital , Ghent , Belgium

2. Belgian Cancer Registry , Brussels , Belgium

3. Department of Neurosurgery, AZ Delta , Roeselare , Belgium

4. Department of Neurosurgery, UZ Leuven , Leuven , Belgium

5. Laboratory for experimental neurosurgery and neuroanatomy, Department of Neurosciences, Leuven Brain Institute (LBI), KU Leuven , Leuven , Belgium

6. Department of Radiation Oncology, Ghent University Hospital , Ghent , Belgium

Abstract

Abstract Background Survival data of diffuse adult-type glioma is mostly based on prospective clinical trials or small retrospective cohort studies. Real-world data with large patient cohorts is currently lacking. Methods Using the nationwide, population-based Belgian Cancer Registry, all known histological reports of patients diagnosed with an adult-type diffuse glioma in Belgium between 2017 and 2019 were reviewed. The ICD-O-3 morphology codes were matched with the histological diagnosis. The gathered data were transformed into the 2021 World Health Organization classification of CNS tumors using the IDH- and 1p/19q-mutation status. Results Between 2017 and 2019, 2233 diffuse adult-type gliomas were diagnosed in Belgium. Full molecular status was available in 67.1% of identified cases. The age-standardized incidence rate of diffuse adult-type glioma in Belgium was estimated at 8.55 per 100 000 person-years and 6.72 per 100 000 person-years for grade 4 lesions. Median overall survival time in IDH-wild-type glioblastoma was 9.3 months, significantly shorter compared to grade 4 IDH-mutant astrocytoma (median survival time: 25.9 months). The 3-year survival probability was 86.0% and 75.7% for grades 2 and 3 IDH-mutated astrocytoma. IDH-wild-type astrocytoma has a worse prognosis with a 3-year survival probability of 31.6% for grade 2 and 5.7% for grade 3 lesions. Conclusions This registry-based study presents a large cohort of adult-type diffuse glioma with known molecular status and uses real-world survival data. It adds to the current literature which is mainly based on historical landmark trials and smaller retrospective cohort studies.

Funder

Stichting Tegen Kanker

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Neurology (clinical),Oncology

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