Frequency and Prognostic Impact of CDKN2A/B Alteration in Oligodendrogliomas: Systematic Review and Meta-analysis

Satoshi Nakasu1, Shoichi Deguchi2,3, Yoko Nakasu4,3

  • 1Division of Neurosurgery, Omi Medical Center.

PubMed

Insights

Homozygous deletion of cyclin-dependent kinase 2A/B (CDKN2A/B-HomoD) is linked to worse survival in molecularly defined oligodendrogliomas. This genetic alteration is more frequent in grade 3 tumors and its detection method impacts reported frequencies.

Area of Science:

  • Neuro-oncology
  • Molecular Pathology
  • Genetics

Background:

  • Isocitrate dehydrogenase (IDH)-mutant astrocytomas with homozygous deletion of cyclin-dependent kinase 2A/B (CDKN2A/B-HomoD) are WHO grade 4.
  • The clinical significance of CDKN2A/B-HomoD in oligodendrogliomas is not well-defined.

Purpose of the Study:

  • To systematically review and meta-analyze the literature on molecularly defined oligodendrogliomas (mOlig).
  • To determine the frequency and prognostic significance of CDKN2A/B gene alterations in mOlig.

Main Methods:

  • Systematic literature review and meta-analysis.
  • Inclusion of studies on molecularly defined oligodendrogliomas (mOlig).
  • Analysis of overall survival and frequency of CDKN2A/B alterations, considering WHO grade and detection methods.

Main Results:

  • Patients with CDKN2A/B-HomoD had significantly worse overall survival (pooled hazard ratio 2.44).
  • CDKN2A/B-HomoD was more frequent in grade 3 mOlig (9.4%) than grade 2 (0.31%).
  • Detection method, particularly fluorescence in situ hybridization (FISH), influenced reported frequencies of CDKN2A/B-HomoD.

Conclusions:

  • CDKN2A/B-HomoD is a significant negative prognostic marker in molecularly defined oligodendrogliomas.
  • The frequency of CDKN2A/B-HomoD varies by tumor grade and detection methodology.
  • Further investigation is needed for other CDKN2A/B alterations like mutation, hemizygous deletion, and promoter methylation.