Patient FAQ
Frequently Asked Questions About Cervical Cancer Screening
Cervical cancer screening involves tests that look for changes in the cells of the cervix that could lead to cancer. The goal is to find and treat these changes *before* cancer develops. The two main tests are the Pap test and the HPV test.[1, 2]
The **Pap test** (or Pap smear) looks for precancers, which are cell changes on the cervix that might become cervical cancer if they are not treated appropriately.[1]
The **HPV test** looks for the human papillomavirus (HPV), the virus that can cause these cell changes.[1]
Sometimes these tests are done together, which is called co-testing.[1]
HPV (Human Papillomavirus) is a very common virus that is the main cause of cervical cancer.[3] Most sexually active people will get HPV at some point in their lives, but the vast majority of infections go away on their own without causing any problems.[4, 3] A positive HPV test does not mean you have cancer; it means you have a virus that could potentially cause problems down the road and should be monitored by your doctor.[5]
The OncoE6™ test is a newer, more specific type of test. A standard HPV test just detects if the virus is present. The OncoE6™ test goes a step further by detecting the E6 oncoprotein, a specific protein that high-risk HPV types 16 and 18 produce only when they are actively causing the changes that can lead to cancer.[6, 7, 8] This helps distinguish a harmless, temporary infection from one that is on a path to cause cancer, helping to avoid unnecessary follow-up procedures.[7]
"Molecular Colposcopy" is a term used to describe the benefit of the OncoE6™ test. A traditional colposcopy is a visual exam where a doctor looks at the cervix with a magnifier to find abnormal areas to biopsy, but it's possible to miss the most serious spot. The OncoE6™ test avoids this "sampling error" by checking the entire cell sample for the molecular signature (the E6 protein) of a high-risk infection, giving a more complete picture of what's happening on the cervix.[9, 10]
HPV infections are extremely common in women in their 20s, but they are almost always temporary and clear up on their own.[4, 11] Because of this, testing for HPV in this age group leads to a high number of "false positives," which can cause unnecessary anxiety and lead to follow-up procedures for an infection that would have resolved naturally.[12, 4] That is why guidelines often recommend only a Pap test for this age group.[13, 2]
Current guidelines suggest that women over 65 can stop screening if they have a history of normal test results.[14, 13] However, women over 65 still account for about 20% of new cervical cancer cases and are more likely to be diagnosed at a late stage.[15, 16] One reason is that hormonal changes after menopause can make Pap tests less accurate and more likely to miss problems.[17, 18, 19]
An abnormal result usually requires a follow-up procedure called a **colposcopy**. This is a simple procedure where your doctor uses a magnifying lens to look at your cervix more closely. If they see a suspicious area, they may take a small tissue sample, called a **biopsy**, for testing.[20]
If a biopsy shows high-grade precancerous cells, your doctor may recommend a **LEEP (Loop Electrosurgical Excision Procedure)**. This procedure uses a thin wire loop with an electric current to remove the abnormal tissue.[21] While LEEP is very effective, it does carry a small risk of affecting future pregnancies, including an increased risk for preterm birth and miscarriage.[22, 23, 21]
Yes. The FDA recently approved HPV self-collection kits that can be used at home. You can collect a vaginal sample yourself and mail it to a lab for testing. This is a great option that can help overcome barriers like lack of time, transportation, or discomfort with pelvic exams.
Yes, studies show comparable accuracy for detecting high-grade changes, especially when using validated, PCR-based tests. One FDA-approved device showed 95% agreement with clinician-collected samples.

