Clinical Validation of An Optimized Multi-Target Stool DNA (Mt-sDNA 2.0) Test, for Colorectal Cancer Screening "BLUE-C"

Exact Sciences Corporation

Status

Completed

Conditions

Colorectal Cancer

Treatments

Procedure: Colonoscopy

Diagnostic Test: FIT test

Diagnostic Test: mt-sDNA 2.0 screening test

Study type

Observational

Funder types

Industry

Identifiers

NCT04144738

2019-01

Details and patient eligibility

About

The primary objective of this study is to assess the sensitivity for colorectal cancer (CRC) and specificity of the mt-sDNA 2.0 test.

Full description

Subjects 40 years of age and older scheduled for a screening colonoscopy will be enrolled. Subject will complete the mt-sDNA 2.0 test and the commercially available FIT, followed by completion of a screening colonoscopy. The results of the mt-sDNA screening test and FIT will not be provided to investigators for clinical management of the study subject. Personnel performing the colonoscopy and producing the resulting report and personnel performing histopathologial review of reports or tissue (if applicable) will remain blinded to the results of the mt-sDNA 2.0 screening test results.

Enrollment

26,758 patients

Sex

All

Ages

40+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Subjects must meet the following criteria to be eligible for the study:

Subject is ≥ 40 years of age at the time of enrollment.
Subject presents for a screening colonoscopy per standard of care.
Subject has no symptoms or signs that require immediate, or near term, referral for diagnostic or therapeutic colonoscopy.
Subject is able and willing to sign informed consent

Exclusion criteria

Subject has a history of CRC or advanced precancerous lesions.
Subject has a diagnosis or medical / family history of any of the following conditions, including:
- Familial adenomatous polyposis (also referred to as "FAP", including attenuated FAP and Gardner's syndrome),
- Hereditary non-polyposis CRC syndrome (also referred to as "HNPCC" or "Lynch Syndrome"),
- Other hereditary cancer syndromes including but are not limited to Peutz-Jeghers Syndrome, MYH-Associated Polyposis (MAP), Turcot's (or Crail's) Syndrome, Cowden's Syndrome, Juvenile Polyposis, Neurofibromatosis, or Familial Hyperplastic Polyposis.
Subject has a diagnosis or personal history of inflammatory bowel disease (IBD) including chronic ulcerative colitis and/or Crohn's disease.
Subject has a diagnosis of Cronkhite-Canada Syndrome.
Subject has had a positive Cologuard within the previous 2 years, or fecal occult blood test or FIT within the previous 6 months.
Subject has undergone a colonoscopy within the previous 9 years with the exception of a failed colonoscopy due to poor bowel preparation. Failed colonoscopy must have been within the past year and without therapeutic intervention.
Subject has had overt rectal bleeding within the previous 30 days.
Subject has any condition that in the opinion of the Investigator should preclude participation in the study.