| Literature DB >> 26211481 |
Abstract
Colorectal cancer (CRC) is the third most commonly diagnosed cancer and the second leading cause of cancer death among men and women combined in the USA. Although the benefits of early CRC detection are widely recognized, screening rates are suboptimal. Cologuard is a multitarget stool DNA screening test that offers a unique non-invasive option for CRC screening. Cologuard was the first product to be reviewed under a pilot parallel review program jointly conducted by the US FDA and the Centers for Medicare & Medicaid Services (CMS). This parallel review process shortened the overall review for Cologuard and resulted in a preliminary National Coverage Determination that coincided with FDA approval.Entities:
Keywords: Cologuard®; FDA-CMS parallel review; colorectal cancer screening; in vitro diagnostic; multitarget stool DNA; premarket authorization; reimbursement; stool DNA testing; stool DNA-based colorectal cancer screening test
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Year: 2015 PMID: 26211481 DOI: 10.1586/14737159.2015.1069184
Source DB: PubMed Journal: Expert Rev Mol Diagn ISSN: 1473-7159 Impact factor: 5.225