© 2005 Oxford University Press
CORRESPONDENCE |
RESPONSE: Re: A Study of the Impact of Adding HPV Types to Cervical Cancer Screening and Triage Tests
Affiliations of authors: National Cancer Institute, National Institutes of Health, U.S. Departments of Health and Human Service, Bethesda, MD (MS, PEC, DS); Department of Pathology, University of Virginia, Charlottesville, VA (MS); Departments of Molecular Genetics and Microbiology and Obstetrics and Gynecology, University of New Mexico, Albuquerque, NM (CMW)
Correspondence to: Mark Schiffman, MD, MPH, Hormonal and Reproductive Epidemiology Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD (e-mail: schiffmm@exchange.nih.gov).
| The first 10% of the full text of this article appears below. |
The use of human papillomavirus (HPV) DNA testing for triage of atypical squamous cells (ASCs or equivocal cytologic specimens) is already widespread, and its promise for general screening is gaining acceptance (1). The value of impending widespread HPV testing will depend on how thoughtfully it is used.
As supported by Franceschi and Clifford's statistically powerful contribution, epidemiologists are reaching agreement concerning
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J Natl Cancer Inst 2005 97: 938-939.