Cervical Cancer

Cervical cancer screening is designed to detect precancerous changes caused by high-risk human papillomavirus (hrHPV) before cancer develops. Two tests are used: the hrHPV test and Pap (cytology); some programs use them together (cotesting). For average-risk people, major guidelines recommend:

  • USPSTF (2018): Pap every 3 years at 21–29; at 30–65 choose primary hrHPV every 5 yearscotesting every 5 years, or Pap every 3 yearsUSPSTF

  • ACS (2020): start at 25 and prefer primary hrHPV every 5 years through 65 (cotesting q5y or Pap q3y are acceptable where primary HPV isn’t available). American Cancer Society MediaRoomCancer.gov

New in the U.S.: the FDA now permits self-collected vaginal samples for hrHPV testing in a health-care setting (e.g., clinic, pharmacy) for certain assays—useful for people who decline a pelvic exam. This does not replace guideline screening, and collection must occur in-clinicCancer.govU.S. Food and Drug Administration


Signs & Situations (When to consider testing)

Screen regularly even without symptoms. Seek medical care promptly for abnormal vaginal bleeding, persistent pelvic pain, or a visible cervical lesion—those require diagnostic evaluation, not screening. asccp.org

Who should screen (average risk):

  • Ages 21–29: Pap every 3 years (USPSTF).

  • Ages 30–65: Primary hrHPV q5y preferred (ACS); alternatives include cotesting q5y or Pap q3y(USPSTF/ACS).

  • Stop after 65 if you’ve had adequate prior negative screening and no history of CIN2+—confirm with your clinician. 

  • After total hysterectomy (cervix removed) for benign reasons and no CIN2+ history: do not screen

High-risk groups (e.g., immunocompromised, prior CIN2+, DES exposure) may need different schedules; follow clinician guidance. 


Why These Tests Matter

What screening can do

  • Find HPV-driven precancers early, reducing cancer incidence and deaths.

  • Tailor follow-up using risk-based management (ASCCP), often allowing surveillance instead of immediate procedures when risk is low. 

What screening cannot do

  • It does not diagnose cancer by itself—colposcopy/biopsy confirms.

  • A normal test does not mean “no future risk”—stay on schedule


What These Tests Measure (at a glance)

  • Primary hrHPV test: detects high-risk HPV types; some assays genotype 16/18 separately to refine risk. Preferred by ACS beginning at age 25. 

  • Pap (cytology): looks for abnormal cervical cells; used alone (q3y) or with hrHPV (cotesting).

  • Self-collected hrHPV (in health-care settings): clinic-based self-swab now authorized for certain tests; programs are still expanding. 


How the Testing Process Works

  1. Choose the pathway based on age and availability (primary hrHPV preferred where offered; Pap or cotesting are acceptable alternatives per guidelines). 

  2. Sample collection: clinician-collected cervical sample, or clinic-based self-collected vaginal sample for approved hrHPV tests.

  3. Results delivered quickly to your secure account (timing varies by test).

  4. Next steps: your clinician applies ASCCP risk-based algorithms to decide on repeat testing vs. colposcopy. 


Interpreting Results (general guidance)

  • hrHPV negative: low immediate risk—return at the routine interval (often 5 years for primary HPV). 

  • hrHPV positive, cytology negative: risk depends on HPV genotype and history; many cases get 1-year repeat testing rather than immediate colposcopy under ASCCP

  • Abnormal cytology (ASC-US/LSIL/HSIL) and/or hrHPV positive: management follows risk thresholds; high-risk results may prompt colposcopy

HPV vaccination reduces risk but doesn’t replace screening—follow age-appropriate schedules. 


Choosing Panels vs. Individual Tests

  • Ages 21–29: Pap q3y (USPSTF).

  • Ages 25–65 (ACS-preferred): primary hrHPV q5y; acceptable alternatives: cotest q5y or Pap q3y if primary HPV isn’t available.

  • Ages 30–65 (USPSTF options): primary hrHPV q5ycotest q5y, or Pap q3y—choose one and stay consistent. 

  • Post-hysterectomy (cervix removed, no CIN2+): stop screening


FAQs

When should I start screening?
USPSTF: 21 (Pap q3y). ACS: 25 (prefer primary hrHPV q5y). Discuss which pathway fits your history and access.

Does HPV vaccination change my schedule?
No. Keep screening on time even if vaccinated.

Can I collect my own sample?
Yes, at Ulta Lab Tests the FDA now allows self-collected vaginal samples for specific hrHPV tests. It’s not at-home testing and doesn’t replace the need for regular screening. 

Do I still need screening after a total hysterectomy?
If your cervix was removed and you have no history of CIN2+ or cervical cancer, routine screening is not recommended.

What happens after an abnormal result?
Clinicians use ASCCP risk-based management to decide on repeat testing vs. colposcopy and follow-up intervals.


Internal Links & Cross-References

  • Cancer Screening Hub

  • Women’s Cancer & Tumor Markers

  • Breast Cancer

  • Ovarian Cancer

  • Multi-Cancer Early Detection (MCED)

  • Key Lab Tests : hrHPV Test • Pap (Cytology) • Cotest • Colposcopy (Clinical Follow-up)


References

  1. U.S. Preventive Services Task Force. Cervical Cancer: Screening. Final Recommendation Statement. 2018.

  2. U.S. Preventive Services Task Force. Cervical Cancer: Screening. Draft Recommendation (update in progress). December 2024.

  3. American Cancer Society. Cervical Cancer Screening Guideline Update. July 2020; web page updated 2025.

  4. National Cancer Institute Cancer Currents Blog. FDA Authorizes Self-Collection for HPV Tests in Health-Care Settings. July 2024.

  5. U.S. Food and Drug Administration. BD Onclarity HPV Assay — approval summary (self-collection expansion). August 2024.

  6. ASCCP. 2019 Risk-Based Management Consensus Guidelines for Abnormal Cervical Cancer Screening Tests and Cancer Precursors (with 2024 updates/corrections).

  7. American College of Obstetricians and Gynecologists (ACOG). Practice Advisory: Updated Cervical Cancer Screening Guidelines (endorsing ASCCP risk-based management). 2021.

Available Tests & Panels 

When cells grow in an uncontrolled and potentially harmful manner in the cervix, cervical cancer is the result. The cervix is the cone-shaped passage that connects the vagina to the lower portion of the uterus. 

A persistent viral infection causes most cases of cervical cancer. The viruses responsible are strains of human papillomavirus or HPV. HPV is transmitted sexually and is extremely common. 

High-Risk HPV: 14 of the different identified strains of HPV are likely to cause cancer. Two of these type 16 and type 18, are responsible for approximately 80 percent of all cervical cancer cases. 

Low-Risk HPV: There are a few strains of HPV that rarely cause cancer, instead usually causing genital warts. HPV-6 and HPV-11 produce ninety percent of all genital warts, but these strains are considered “low-risk” for cervical cancer. 

The human body is often able to clear an HPV infection without medical treatment. When a high-risk HPV strain goes untreated and is not cleared by the body, it can eventually cause cervical cancer. The development process that leads from the infection to cancer takes many years. High-risk HPV strains cause the uncontrolled growth of infected cells in the cervix. The body’s immune system will usually recognize these cells as unwanted and limit their growth. If the cells remain and develop, they can become precancerous. 

Precancerous cells may be found on the outside or the inside of the cervix. They are visually different from normal, healthy cells. Precancerous and cancerous cervix cells start on the linings of the cervix. If they are not treated, they can become invasive and start spreading into the deeper tissues of the cervix. From there, they may eventually spread throughout the body. 

Cervical cancer can be divided into two broad categories: 

Squamous cell carcinoma: These are cancers in the squamous (flat) cells that line the outside of the cervix. Squamous cell carcinoma accounts for the great majority of cervical cancer cases. Data collected by the American Cancer Society suggests that nine out of 10 cervical cancer cases are squamous cell carcinoma. 

Adenocarcinomas: Most remaining cases of cervical cancer are adenocarcinomas. In these cancers, the faulty cells start in the mucus-producing glands at the opening of the cervix, the endocervix. 

On very rare occasions, a case of cervical cancer may involve both types of cancer cells growing in the same patient. 

Cervical cancer can be successfully treated by surgically removing the cancerous cells. This is particularly effective when the cancer is detected early. Women who are treated for early-stage cervical cancer have a 5-year survival rate of more than 90 percent. 

If the cancer spreads beyond the cervix’s surface, effective treatment may require a hysterectomy, chemotherapy, and/or radiation treatment. The longer cervical cancer goes untreated, the greater its chance of spreading (metastasizing) to nearby tissues and organs. The uterus, bladder, rectum, and abdominal wall are all at risk. Cervical cancer can spread throughout the entire body if it first reaches the pelvic lymph nodes. Survival rates and rates of successful treatment decline as cases grow further beyond the initial organ. Widespread cervical cancer is usually fatal. 

According to the American Cancer Society, yearly diagnoses of cervical cancer in the US exceed 13,000 cases. Each year, 4,250 women are likely to die of the disease. In the past, invasive cervical cancer was a far more common and serious disease in the US.  

The Papanicolaou smear (commonly called the Pap smear or Pap test) has dramatically improved detection rates for cervical cancer. This screening test allows for the early and accurate detection of cancerous and precancerous cells in the cervix. Its adoption has reduced cervical cancer rates in industrialized nations (including the US) by up to 70 percent. The latest additions to the cervical cancer detection toolkit are accurate tests that can detect the presence of specific high-risk strains of HPV. 

While the detection and treatment of cervical cancer have improved considerably, the disease is still a serious threat, particularly in certain US populations at increased risk. Hispanic women, for example, have the highest cervical cancer rates. The disease is also more serious in developing nations, where women have limited access to tests and healthcare. The World Health Organization asserts that cervical cancer is the second-most common form of cancer among female populations in developing nations. The developing world sees more than half a million new cervical cancer diagnoses every year. Eighty-five percent of deaths related to cervical cancer occur in developing nations. 

Risk Factors:

As already noted, a persistent infection with a strain of human papillomavirus (HPV), particularly a high-risk one, is the key risk factor for cervical cancer. 

The National Cancer Institute does note that other factors can make cervical cancer development more likely after you have an HPV infection. The key secondary factors are long-term use of oral contraceptives (birth control pills), bringing three or more pregnancies to term, and smoking. 

These conditions can also increase the risk of cervical cancer: 

  • A weakened or compromised immune system (e.g., with an HIV infection or following an organ transplant) 
  • An unhealthy diet lacking fruits and vegetables 
  • Being overweight 
  • A history of cervical cancer in older relatives 
  • A history of chlamydia infection 
  • A history of DES exposure before birth (DES is a drug given to some pregnant women from 1940 to 1971 to prevent miscarriages) 

Signs and Symptoms  

Neither an HPV infection nor precancerous cell growth in the cervix normally causes any detectable symptoms. Testing is the only way to find out if either condition is present. 

General symptoms that may be caused by cervical cancer include abnormal bleeding between menstrual periods, bleeding after intercourse, or increased vaginal discharge. These symptoms usually only appear after cervical cancer has fully developed and become invasive; the cancer may already have spread to other tissues. 

Note that these symptoms can be caused by a wide range of conditions other than cervical cancer. Talk to a healthcare provider to find out what is causing any such symptoms. You should also establish a schedule for preventive cervical cancer screening if you do not have symptoms. 

Tests 

  • Pap Smear (AKA Pap Test) 

The Papanicolaou (Pap) smear is an effective, widely used test that screens for precancerous or cancerous changes in the cervix. Cells on the inside and outside lining of the cervix start to change appearance as soon as they become precancerous. When detected on a Pap smear, such different cells are called “atypical cells.” The presence of precancerous cells is not the only condition that can lead to atypical cells; they may also appear if the cervix lining is irritated or the patient has an infection. The appearance of atypical cells continues to change as they grow toward cancer. Intermediate cellular changes detected in a Pap smear are called low or high-grade squamous intraepithelial lesions. 

  • HPV Test 

The HPV test is a cervical cancer screening test that is primarily administered to women who are over the age of 30. HPV testing may be performed on younger women if they are at increased risk of developing cervical cancer. The test detects any infection with high-risk strains of human papillomavirus (hrHPV). If such an infection becomes persistent, it can start causing cervical cell changes that may lead to the development of cancer. With the link between hrHPV infection and cervical cancer now thoroughly established, HPV testing is a key part of women’s health screening. 

  • Recommendations 

A range of different professional organizations is in broad agreement on the best practices for cervical cancer screening. Recommendations are largely the same from the American Cancer Society, the American Society for Clinical Pathology (ASCP), the American College of Obstetricians and Gynecologists (ACOG), the US Preventive Services Task Force (USPSTF), the Society of Gynecologic Oncology and the American Society for Colposcopy and Cervical Pathology (ASCCP). 

Women between the ages of 30 and 65 are advised to discuss the benefits and drawbacks of the screening strategies described below with their healthcare providers. 

Preferred – Co-testing every five years with a Pap smear and a high-risk HPV (hrHPV) test 

Acceptable – Pap smears every three years 

Alternative – hrHPV tests every five years 

Pap smears are recommended at three-year intervals for women between the ages of 21 and 29. HPV testing is only recommended if a Pap test shows abnormal changes. 

Screening is not recommended for women under the age of 21 because cervical cancer is rare in this age group. False-positive results become too frequent in this age group, leading to unwanted stress and unnecessary treatment. 

Women over the age of 65 do not need screening if they have not experienced any abnormal cervical changes in the past.

One of the two following testing situations should also be true: 

  • Your last three Pap smears have been negative or 
  • You have had two negative co-tests (Pap smear hrHPV) in the last ten years, with the most recent being no more than five years ago. 

It is important to continue regular screening for cervical cancer even if you receive the HPV vaccine. (See prevention.) 

Your healthcare provider should schedule screening more frequently if you have any increased risk factors for cervical cancer, including: 

  • DES (diethylstilbestrol) exposure when your mother was pregnant with you 
  • HIV infection 
  • Immune system compromise 
  • Previous diagnoses of cervical cancer or a high-grade precancerous lesion