Senior Editor, OncLive®
Jason Harris has worked in journalism for more than 20 years, including stints at daily newspapers and niche publications for oncology and cardiology. He is a senior editor for OncologyLive® and managing editor for Oncology Fellows and the annual Giants of Cancer Care® album. He also contributes to the OncLive On Air and OncFellows podcasts. Email: email@example.com
The FDA announced that it has approved the FoundationOne CDx assay. The Centers for Medicare & Medicaid Services issued a simultaneous announcement saying the next-generation sequencing-based in vitro diagnostic test will be covered by insurance.
The FDA has approved the FoundationOne CDx (F1CDx) cancer biomarker assay concurrently with a decision from the Centers for Medicare & Medicaid Services (CMS) to provide insurance coverage for the next-generation sequencing (NGS)-based in vitro diagnostic (IVD) test.
F1CDx, which detects 324 different genes, is a "more extensive" assay that can identify actionable mutations across 5 tumor types for 15 different targeted therapies. Additionally, the assay can detect microsatellite instability and tumor mutational burden, which have been associated with response to immunotherapy. In clinical trial results, F1CDx could accurately detect substitutions, short insertions, and deletions approximately 94.6% of the time for each of the 324 genes, according to the FDA.
The agency said the test can be used as a companion diagnostic to identify specific mutations for non—small cell lung cancer, melanoma, breast cancer, colorectal cancer, or ovarian cancer. The F1CDx can detect genetic mutations that are indicated for multiple treatments, extending beyond the previous “one test for one drug” model. Among the 324 genes, the F1CDx assay can detect alterations in EGFR, KRAS, BRAF, BRCA1/2, ALK, and several other genes with emerging therapeutics, such as NTRK1/2/3.
“The F1CDx can help cancer patients and their healthcare professionals make more informed care decisions without the often-invasive process of extracting tumor samples multiple times to determine eligibility for a single treatment or enrollment in a clinical trial,” Jeffrey Shuren, MD, director of the FDA’s Center for Devices and Radiological Health (CDRH), said in a press release. “With the run of one test, patients and health care professionals can now evaluate several appropriate disease management options.”
CMS issued a proposed national coverage determination of the F1CDx and other similar NGS IVDs for Medicare beneficiaries with recurrent, metastatic, or advanced stage IV cancer who have not been previously tested using the same NGS technology and continue to seek further cancer therapy. Use of a test as a diagnostic also includes the ability to help patients and their treating physicians determine candidacy for clinical trials.
The test is the second IVD to be approved and covered after overlapping review by the FDA and CMS under the Parallel Review Program, a voluntary program that designed to help Medicare beneficiaries get earlier access to innovative medical technologies.
“By leveraging two policy efforts aimed at expediting access to promising new technologies, we’ve been able to bring patients faster access to a breakthrough diagnostic that can help doctors tailor cancer treatments to improve medical outcomes and potentially reduce health care costs,” said FDA Commissioner Scott Gottlieb, MD. “The FDA’s Breakthrough Device Program and Parallel Review with CMS allowed the sponsor to win approval for this novel diagnostic and secure an immediate proposed Medicare coverage determination within six months of the FDA receiving the product application.”
The F1CDx had not been previously submitted for the FDA’s review because it is a laboratory-developed test. The agency has not generally enforced premarket review and other applicable requirements for such tests. However, at the request of Foundation Medicine, developer of the F1CDx, the FDA approved the assay for the newly established Breakthrough Device Program because of the test’s potential to consolidate multiple companion diagnostic claims for patients and healthcare providers in a single test.
Under the Breakthrough Device Program, the FDA provides intensive interaction and guidance to the company on efficient device development the agency’s review of devices that provide for more effective treatment or diagnosis for life-threatening or irreversibly debilitating diseases for which no approved or cleared treatment exists or that offer significant advantages over the existing standard of care.