My watch list  

FDA Approves Roche’s HPV Test for Identifying Women at Highest Risk for Cervical Cancer


Roche announced that the US Food and Drug Administration (FDA) has approved the cobas HPV (Human Papillomavirus) Test which identifies women at highest risk for developing cervical cancer. This test will help physicians make early, more accurate decisions about patient care, which may prevent many women from developing this deadly disease.

The cobas HPV Test is the only FDA-approved cervical cancer screening test that allows HPV 16 and 18 genotyping concurrently with high-risk HPV testing. It individually identifies genotypes 16 and 18, the two highest-risk HPV genotypes responsible for more than 70 percent of cervical cancer cases, while simultaneously detecting 12 other high risk HPV genotoypes. The approval was based on data from the ATHENA study involving more than 47,000 women in the US. Results demonstrated that 1 in 10 women, age 30 and older, who tested positive for HPV 16 and/or 18 by the cobas HPV Test actually had cervical pre-cancer even though they showed normal results with the Pap test.

“The FDA approval of the cobas HPV Test demonstrates the value of simultaneous HPV 16 and 18 genotyping in cervical cancer screening,” said Daniel O’Day, Chief Operating Officer of Roche Diagnostics. “We look forward to working with laboratories and physicians to introduce the cobas HPV Test into routine cervical cancer screening.”

More than 55 million Pap cytology (“Pap smear”) tests are performed in the US annually. Current guidelines for screening allow for either cytology or cytology plus HPV testing to determine the risk of cervical cancer. However, HPV testing, and 16 and 18 genotyping in particular, identifies more women at risk earlier than Pap cytology testing alone.

“Screening for high-risk HPV genotypes provides important additive information to Pap testing, and screening for the two highest risk types, HPV 16 and 18 can provide predictive information about a woman’s risk for having cervical pre-cancer or cancer,” said Mark H. Stoler, MD, Professor and Associate Director of Surgical Pathology and Cytopathology, at the University of Virginia Health System. “The cobas HPV Test provides physicians with a validated tool that helps them make early and more informed decisions regarding patient care.”

Facts, background information, dossiers
More about Roche
  • News

    Roche to restructure its manufacturing network for small molecules

    Roche announced plans to restructure its manufacturing network for small molecules to address current underutilisation as a result of its evolving portfolio. A new generation of specialised medicines based on small molecules requires novel manufacturing technologies and will be produced in ... more

    Roche to acquire Kapa Biosystems

    Roche announced that it has signed a definitive agreement to acquire Kapa Biosystems, Inc. (Kapa) a privately-held company headquartered in Wilmington, Massachusetts, US. Kapa Biosystems is a provider of genomic tools in the life sciences sector that employs proprietary technologies to opti ... more

    Evotec's partner Roche provides initial update from Phase IIb trial in Alzheimer's disease

    Evotec AG was updated today by its partner Roche on the initial results of the Phase IIb trial with Sembragiline (RG1577, EVT302), a MAO-B inhibitor for the treatment of Alzheimer's disease ("AD"). In this study, Sembragiline failed to demonstrate benefit on the primary endpoint (Alzheimer' ... more

  • Companies

    Roche Deutschland Holding GmbH


    Roche Austria GmbH

    Headquartered in Basel, Switzerland, Roche is a leader in research-focused healthcare with combined strengths in pharmaceuticals and diagnostics. Roche is the world’s largest biotech company with truly differentiated medicines in oncology, virology, inflammation, metabolism and CNS. Roche i ... more

More about FDA
Your browser is not current. Microsoft Internet Explorer 6.0 does not support some functions on Chemie.DE