PT  - JOURNAL ARTICLE
AU  - Rola H Ali
AU  - Mona Alateeqi
AU  - Hiba Jama
AU  - Noor Alrumaidhi
AU  - Ali Alqallaf
AU  - Eiman Mahmoud Mohammed
AU  - Maryam Almurshed
AU  - Shakir Bahzad
TI  - Evaluation of the Oncomine Comprehensive Assay v3 panel for the detection of 1p/19q codeletion in oligodendroglial tumours
AID  - 10.1136/jclinpath-2021-207876
DP  - 2023 Feb 01
TA  - Journal of Clinical Pathology
PG  - 103--110
VI  - 76
IP  - 2
4099  - http://jcp.bmj.com/content/76/2/103.short
4100  - http://jcp.bmj.com/content/76/2/103.full
SO  - J Clin Pathol2023 Feb 01; 76
AB  - Aims Accurate assessment of 1p/19q codeletion status in diffuse gliomas is of paramount importance for diagnostic, prognostic and predictive purposes. While targeted next generation sequencing (NGS) has been widely implemented for glioma molecular profiling, its role in detecting structural chromosomal variants is less well established, requiring supplementary informatic tools for robust detection. Herein, we evaluated a commercially available amplicon-based targeted NGS panel (Oncomine Comprehensive Assay v3) for the detection of 1p/19q losses in glioma tissues using an Ion Torrent platform and the standard built-in NGS data analysis pipeline solely.Methods Using as little as 20 ng of DNA from formalin-fixed paraffin-embedded tissues, we analysed 25 previously characterised gliomas for multi-locus copy number losses (CNLs) on 1p and 19q, including 11 oligodendrogliomas (ODG) and 14 non-oligodendroglial (non-ODG) controls. Fluorescence in-situ hybridisation (FISH) was used as a reference standard.Results The software confidently detected combined contiguous 1p/19q CNLs in 11/11 ODGs (100% sensitivity), using a copy number cut-off of ≤1.5 and a minimum of 10 amplicons covering the regions. Only partial non-specific losses were identified in non-ODGs (100% specificity). Copy number averages of ODG and non-ODG groups were significantly different (p<0.001). NGS was concordant with FISH and was superior to it in distinguishing partial from contiguous losses indicative of whole-arm chromosomal deletion.Conclusions This commercial NGS panel, along with the standard Ion Torrent algorithm, accurately detected 1p/19q losses in ODG samples, obviating the need for specialised custom-made informatic analyses. This can easily be incorporated into routine glioma workflow as an alternative to FISH.All data relevant to the study are included in the article or uploaded as supplementary information.