The updated recommendation expands cervical cancer screening options to include certain FDA-approved self-collection tests.

In early December, the American Cancer Society updated its guidelines for the first time since 2020. Now, all women ...

HPV self-tests allow patients to collect a sample themselves, instead of having a healthcare provider collect it.

The U.S. Food and Drug Administration has approved the country’s first at-home HPV screening device. The test is designed as an alternative to the Pap smear, a procedure that detects precancerous ...

A revolutionary development in cervical cancer screening is transforming the way millions of women approach their health care. The FDA’s recent approval of self-collection kits from leading healthcare ...

Pap smears are a vital tool for preventing cervical cancer because they can detect cell abnormalities before they become cancerous. Unfortunately, systematic barriers or a lack of comfort with the ...

Roche’s CINtec PLUS Cytology is the only FDA-approved and CE-marked dual-stain test to triage human papillomavirus (HPV)-positive cervical cancer screening test results Dual-stain biomarkers aid in ...

Investigators examined cervical cancer screening guideline adherence among a nationally representative commercially insured cohort in the US to identify factors and modalities associated with ...

Factors Influencing the Experience of Breast and Cervical Cancer Screening Among Women in Low- and Middle-Income Countries: A Systematic Review A literature search was performed in PubMed, Embase, and ...