Core Insights - Quest Diagnostics has launched a new FDA-cleared HPV self-collection solution to enhance access to HPV screening, aiming to identify women at risk of cervical cancer [1][4][5] - The self-collection option will be available in physician offices and at 2,000 Quest patient service centers across the United States starting next month [2][3] - The initiative follows the successful introduction of self-collection services for other STIs in October 2024, indicating strong demand for discreet self-collection options [2][4] Company Strategy - The new self-collection service allows patients to collect specimens privately, which may help reduce barriers to screening and increase participation among women who might otherwise avoid traditional methods [5][6] - Quest Diagnostics emphasizes the importance of providing options for patients who may feel uncomfortable with clinician-collected tests due to various personal factors [6][7] - The company aims to address the significant decline in cervical cancer screenings, with 4.4 million fewer American women screened in 2021 compared to 2019, and a 1.7% increase in cervical cancer incidence among women aged 30-44 during the same period [6][7] Industry Context - The self-collection method is recognized for its accuracy and potential to increase screening rates in historically underscreened populations, aligning with recent guidelines from the United States Preventive Services Task Force [6][7] - The initiative reflects a broader trend in the healthcare industry towards empowering patients and improving access to preventive care [4][6]
Quest Diagnostics Introduces HPV Specimen Self-Collection for Cervical Cancer Screening