To investigate the current practice of HPV-specific testing in oropharyngeal squamous cell carcinoma among head and neck pathologists in the UK and Ireland.
Approach:
Survey Methodology: A survey was conducted among consultant head and neck pathologists in the UK and Ireland, receiving forty-four valid responses.
Key Findings:
100% of respondents had access to P16 immunohistochemistry in-house.
91% had access to HPV-specific testing, primarily PCR, but only 25% had it in-house.
Median turnaround time for HPV-specific testing was 14 days compared to 2 days for P16 immunohistochemistry.
36% of respondents requested HPV-specific testing based on clinical suspicion.
Limitations:
The survey had a limited number of respondents (44), which may not represent all practices.
Responses were predominantly from England, potentially skewing the results.
Conclusion:
There is significant variability in HPV-specific testing practices across the UK and Ireland.