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Updated: Aug 15, 2025

Chromogenic In Situ Hybridization as a Tool for HPV-Related Head and Neck Cancer Diagnosis
Published on: June 14, 2019
IPVS policy statement on HPV nucleic acid testing guidance for those utilising/considering HPV as primary precancer
Suzanne M Garland1, Thomas Iftner2, Kate Cuschieri3
1Department of Obstetrics and Gynaecology, University of Melbourne, Parkville 3052, Victoria, Australia; Centre for Women's Infectious Diseases Research, The Royal Women's Hospital, Parkville 3052, Victoria, Australia; Infection and Immunity, Murdoch Children's Research Institute, Parkville 3052, Victoria, Australia.
Abstract:
We advise that only clinically validated HPV assays which have fulfilled internationally accepted performance criteria be used for primary cervical screening. Further, assays should be demonstrated to be fit for purpose in the laboratory in which they will ultimately be performed, and quality materials manuals and frameworks will be helpful in this endeavor. Importantly, there is a fundamental shortage of well validated, low-cost, low complexity HPV tests that have demonstrated utility in a near-patient setting; representing a significant challenge and focus for future development in order to reach the WHO's goal of eliminating cervical cancer.
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