HPV DNA testing detects viral DNA—even when the virus is not actively producing cancer-causing proteins.
That insight can help support screening decisions, streamline triage, and expand screening access—giving practices more ways to support patients across the cervical cancer screening journey.
High sensitivity helps support confidence in negative results and guideline-aligned 3- or 5-year screening intervals.2-4
HPV DNA testing provides individual results for HPV 16 and HPV 18, plus pooled results for 12 other high-risk genotypes—without additional reflex testing.5 These results can help support timely, guideline-aligned decisions.
Patient self-collection provides another option for HPV screening, either in the office or at a Quest Patient Service Center. Built-in assay controls help confirm the presence of human cellular material and monitor for possible contamination, helping support sample quality and technical performance.
Quest offers co-testing, reflex testing, and individual test codes to support different clinical workflows and patient needs.
* The cobas® HPV Test is indicated for routine cervical cancer screening as per professional medical guidelines, including triage of ASC-US cytology, co-testing (or adjunctive screen) with cytology, and HPV primary screening of women to assess the risk for cervical precancer and cancer. Patients should be followed-up in accordance with professional medical guidelines, results from prior screening, medical history, and other risk factors. Refer to the package insert for detailed information.
References
Let’s talk about how HPV DNA testing can support screening insight, triage, and flexibility.
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Interested in a deep dive on HPV DNA assay design? Learn more from the experts in this webinar from Roche Diagnostics.
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