Cervical cancer screening program and Human Papillomavirus (HPV) testing, part II: Update on HPV primary screening
Arbyn M, Haelens A, Desomer A, Verdoodt F, Thiry N, Francart J, Hanquet G, Robays J
Record ID 32015000810
English
Authors' objectives:
THE PROBLEM ADDRESSED BY THIS REPORT
This report is an update of the report KCE report vol. 38C 4 on the place of HPV in cervical screening. It assesses the impact of HPV screening compared to cytology screening. This report will therefore addresses 3 questions:
- What is the optimal algorithm for cervical cancer screening?
- What is the organisational impact of HPV screening and the way it is organized?
- What is the cost-impact of the introduction of a new screening algorithm?
Authors' results and conclusions:
KEY FINDINGS
- HPV testing is more sensitive for precancerous lesions CIN2 and CIN3 than cytology. The downside is that the transversal specificity is lower.
- The protective effect of HPV screening compared to cytology on the incidence of invasive cervical cancer is directly demonstrated in randomized trials.
- No protective effect is demonstrated under 30 years.
- The risk of CIN3+ or invasive cervical cancer after a negative hrHPV DNA test is significantly lower than after a negative Pap smear. This means that screening intervals can be extended safely up to five and more.
- A two-step triage scenario with twice cytology at cutoff ASC-US+ offers a good balance of efficiency (4 to 9 referrals to detect one CIN3+, ~40% of referral) and safety (risk of CIN3+ in triage-negative women of 0.5%
to 0.9%).
- For the interpretation of cervical cytology specimen, there is no quality control programme yet.
- In Belgium, an ISO15189 accreditation (including participation in external quality assessments) for high-risk HPV detection in cervicovaginal samples using a molecular method - but not for cytopathology - is mandatory for reimbursement.
- The use of colposcopies in Belgium, with high numbers performed without previous cytology result is not in line with the internationally agreed recommendations, where colposcopies should be used to examine women with abnormal cytology findings.
- Proportions of abnormal cytology results varies widely between laboratories.
- It is unlikely that the introduction of HPV screening would lead to a large increase in confirmation tests in the Belgian context.
- HPV screening every 5 year is a dominant option, compared to current practice of cytology screening every 3 years.
Details
Project Status:
Completed
Year Published:
2015
URL for published report:
https://doi.org/10.57598/R238C
URL for additional information:
https://kce.fgov.be/en/publications/all-reports/cervical-cancer-screening-program-and-human-papillomavirus-hpv-testing-part-ii-update-on-hpv-primary
English language abstract:
An English language summary is available
Publication Type:
Rapid Review
Country:
Belgium
DOI:
10.57598/R238C
MeSH Terms
- Early Detection of Cancer
- Female
- Papillomavirus Infections
- Cervical Intraepithelial Neoplasia
Contact
Organisation Name:
Belgian Health Care Knowledge Centre
Contact Address:
Administrative Centre Botanique, Doorbuilding (10th floor), Boulevard du Jardin Botanique 55, B-1000 Brussels, Belgium tel: +32 2 287 33 88 fax: +32 2 287 33 85
Contact Name:
info@kce.fgov.be
Contact Email:
info@kce.fgov.be
Copyright:
<p>Belgian Health Care Knowledge Centre (KCE)</p>
This is a bibliographic record of a published health technology assessment from a member of INAHTA or other HTA producer. No evaluation of the quality of this assessment has been made for the HTA database.