Breast Cancer Resources

for Healthcare Providers

The Utah Breast & Cervical Cancer Screening Program provides cancer screenings to Utah women who are low income and uninsured, or underinsured. We serve:

  • Women aged 40 and older for breast cancer screening
  • Women aged 21-64 for cervical cancer screening

Free screenings may include:

  • Mammogram
  • Pap test
  • Blood pressure
  • Cholesterol
  • Blood sugar

Guidelines and Legislation

Federal guidelines

The Utah Breast & Cervical Cancer Screening Program is funded by a grant from the CDC’s National Breast and Cervical Cancer Early Detection Program (NBCCEDP).

Learn more about the NBCCEDP on the CDC website.

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Visit the U.S. Preventive Services Task Force (USPSTF) website for breast cancer screening recommendations.

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Learn more about early detection and diagnosis from American Cancer Society’s website.

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To improve access to cancer screening, Congress passed the Breast and Cervical Cancer Mortality Prevention Act of 1990.

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Utah Breast & Cervical Cancer Program

The Breast & Cervical Cancer Screening Program contracts with surgeons, obstetricians, gynecologists, and gynecologic oncologists for reimbursement for specified diagnostic and follow-up procedures for clients who qualify for our program.

The program also contracts with various types of facilities.

If your office would like to work with our program, please call 1-800-717-1811

Providers are reimbursed at Medicare rates.  We are unable to pay for treatment.

The B&C Program has approved the inclusion of self-collection HPV testing for cervical cancer screening. This update utilizes the current CPT codes for HPV testing. It’s important to note the following key points:

  • HPV self-collection is for women ages 25-65 for primary HPV screening.
  • HPV self-collection must be completed in a clinic under the supervision of a provider.
  • Clinician-collected primary HPV testing is preferred over co-testing.
  • Currently, only the BD Onclarity and Roche Cobas test kits are FDA-approved for self-collection, and no other kits should be used for this purpose.
  • HPV self-collection is not recommended for individuals at high risk or for surveillance following specific diagnoses.
  • When self-collected vaginal specimens are HPV-negative in the screening setting, repeat testing in 3 years is recommended.
  • When self-collected vaginal specimens are positive for HPV 16 and/or 18, direct referral for colposcopy with concurrent cytology collection is recommended.
  • When self-collected vaginal specimen HPV test results are: a) positive for HPV (untyped), b) negative for HPV 16/18 and positive for HPV HR12 (other); or c) negative for HPV 16/18 and positive for HPV 45, 33/58, 31, 52, 35/39/68, 51 or combinations thereof, obtaining a clinician-collected cervical specimen for cytology or dual stain is recommended. Subsequent management of cytology or dual-stain results per management guidelines is recommended.
  • When self-collected vaginal specimen HPV test results are positive for HPV types 56/59/66 and no other carcinogenic types, 1 year repeat testing is recommended. If HPV-positive for any HPV type at the 1-year follow-up, colposcopy is recommended.
  • The Enduring Guidelines Committee recommends self-collection HPV testing every 3 years. In contrast, the draft guidelines from the U.S. Preventive Services Task Force (USPSTF) suggest self-collection HPV testing every 5 years. The final USPSTF recommendations have not yet been published.

Please refer to the ASCCP Guidelines for Self-Collected HPV Screening (Journal of Lower Genital Tract Disease) article for further details and exclusions to the new guidelines.

Training resources

Webinars

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Videos

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Database instructional resources

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