| Methods |
Performance |
Advantages |
Drawbacks |
| Stool/blood-based tests |
|
|
|
| FITa (stool) |
79% sensitivity 94% specificity |
Noninvasive; Nocomplications; Home-based test. |
Positive results require colonoscopy; test repeated annually; low sensitivity for advanced adenomas; insensitive to serrated lesions. |
| MT-sDNA (stool) |
92% sensitivity 87% specificity |
Noninvasive with no complications; Home-based test; better sensitivity for late-stage adenomas and lesions than FIT alone. |
Positive results need colonoscopy; repeat every 3 years; more expensive than FIT alone. Concerns for false positive. |
| Septin-9 (blood) |
48% sensitivity 91% specificity |
Minimally invasive; no complications; test can be added to usual blood draw. |
Low sensitivity for CRC. Requires colonoscopy for positive results. |
| Visual tests |
|
|
|
| Colonoscopy |
100% detection |
Both diagnostic and therapeutic; can detect cancers and precursor polyps. |
Depends on the skill of operator; bowel preparation and sedation necessary; Risk of complications < 0.1%. |
| Flexible sigmoidoscopy |
90% - 100% sensitivity for distal CRC |
Less invasive than colonoscopy; low risk of complications. |
Colonoscopy needed for positive results; Need to repeat every 5 - 10 years; enema preparation is a pre-requisite. |
| CT colonography |
90% - 100% for CRC; variable sensitivity for polyps and poor sensitivity for lesions. |
Less invasive than colonoscopy; sedation not required; lower risk of complications than colonoscopy. |
Colonoscopy for positive results; bowel preparation is necessary; trained radiologists are inadequate across USA. |
| Colon capsule |
81% sensitivity 93% specificity for polyps ≥ 6 mm |
Minimally invasive. Does not require sedation; newer generation tests are home-based. |
Colonoscopy needed for positive results; Requires bowel preparation. |