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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.
Abstract:
Isocitrate dehydrogenase (IDH) -mutant astrocytomas with homozygous deletion of cyclin-dependent kinase 2A/B (CDKN2A/B-HomoD) are categorized to grade 4 in the new World Health Organization (WHO) classification. However, the clinical implications of CDKN2A/B-HomoD in oligodendrogliomas remain unclear. This study systematically reviewed and meta-analyzed the literature on molecularly defined oligodendrogliomas (mOlig) to find the frequency and prognostic significance of CDKN2A/B gene alterations. Overall survival was worse in patients with CDKN2A/B-HomoD [pooled hazard ratio (pHR) 2.44; 95% confidential interval (CI), 1.59-3.76; P < 0.0001; 7 studies, 1,012 patients] than in those without CDKN2A/B-HomoD. Although the frequency (95% CI) was very low in grade 2 tumors (0.31%; 0.02-0.4) than in grade 3 tumors (9.4%; 6.2-14.0; I2 = 52.0%), pHR of multivariate analyses with covariates of WHO grade and age was still significant (P = 0.017). In contrast, the method in CDKN2A/B evaluation was a significant factor for the heterogeneity in frequency. The pooled frequency of CDKN2A/B-HomoD in grade 3 mOlig by fluorescence in situ hybridization (FISH) (20.3%) was higher than that by other methods (7.3%; P < 0.0006), probably due to the lower threshold for CDKN2A/B-HomoD in FISH studies that was used in this analysis. The frequency (95% CI) of other alterations of the CDKN2A/B gene, i.e., mutation, hemizygous deletion, and promoter methylation, was estimated as 1.48% (0.6-3.5), 15.9% (9.8-24.7), and 20.6% (13.7-29.8), respectively. The clinical significance of these alterations remains unclear due to the immaturity of the investigations.
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.
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