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FDA Recognises OncoKB Database of Molecular Tumour Marker Information

A portion of the OncoKB is recognised as a source of valid scientific evidence for Level 2 and Level 3 biomarkers
08 Oct 2021
Molecular Oncology

On 7 October 2021, the US Food and Drug Administration (FDA) granted recognition to a partial listing of the Memorial Sloan Kettering Cancer Center’s Oncology Knowledge Base (OncoKB) as the first tumour mutation database to be included in the Public Human Genetic Variant Database.

FDA recognised a portion of the OncoKB as a source of valid scientific evidence for Level 2 (clinical significance) and Level 3 (potential clinical significance) biomarkers. Under the FDA’s database recognition programme, test developers can use these data to support the clinical validity of tumour profiling tests in premarket submissions.

Determining the mutation profile of a tumour using DNA sequencing enables the use of targeted therapies and investigational treatment options.

The OncoKB database contains detailed information regarding specific alterations in 682 cancer genes. The information is curated from various world-wide sources, including government agencies, medical professional groups, medical and scientific literature, and clinical trials.

FDA reviewed the operating and governance procedures and policies, processes for the database and for variant evaluation and curation, and method of assignment of clinical significance. The data are sorted into one of two levels of clinical significance consistent with FDA-authorised tumour profiling tests and displayed on a tab referred to as FDA recognised alterations.

View the OncoKB database here.

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