Literature DB >> 31356722

Five-year risk of CIN3 after short-term HPV-DNA negativity in cytology-negative women: a population-based cohort study.

A Del Mistro1, P Giorgi Rossi2, H Frayle1, L Pasquale3, C Campari4, G Ronco5, M Zorzi6.   

Abstract

OBJECTIVE: To assess the 5-year risk of high-grade lesions in women with a transient high-risk HPV infection.
DESIGN: Population-based cohort study.
SETTING: HPV primary testing within population-based organised cervical cancer screening programmes. POPULATION: Italian women enrolled in seven pilot projects and attending the second round.
METHODS: On the basis of the cytology triage performed on HPV-positive women, immediate colposcopy or HPV repeat at 12 months was recommended. Data were collected at the subsequent round 3-4 years after HPV infection clearance. MAIN OUTCOME MEASURES: Rates of HPV infection, CIN2+ and CIN3+ detection at subsequent round after HPV clearance, and relative risks (RR) in comparison with HPV-negative women (with 95% confidence interval).
RESULTS: Data on 1230 women (1027 aged 25-64 years and 203 aged 35-64 years) have been analysed. Overall compliance with repeat HPV testing was 84%. In comparison with HPV-negative women, those with a transient HPV infection had higher proportions of HPV positivity (15% versus 3.7%) and of CIN2+ lesions (0.87% versus 0.23%) in round two; most of these (7/10) were CIN2; no cancers were detected, and CIN3 occurred in 3/1230 (0.24%).
CONCLUSIONS: HPV-based protocols for cervical cancer screening allow long intervals for HPV-negative women; it is important to monitor the clinical outcome in the women with transient high-risk HPV infection. CIN3 detection is similar to that observed in routine European cytology-based screening programmes (CIN3+: 2.7‰); 5-year intervals may provide reasonable protection but longer intervals are not recommended. TWEETABLE ABSTRACT: A screening interval of 5 years (but no longer) appears safe in women with transient HPV detection.
© 2019 Royal College of Obstetricians and Gynaecologists.

Entities:  

Keywords:  zzm321990HPVzzm321990; CIN2; CIN3; Cervical cancer screening; screening interval; transient infection

Mesh:

Year:  2019        PMID: 31356722     DOI: 10.1111/1471-0528.15893

Source DB:  PubMed          Journal:  BJOG        ISSN: 1470-0328            Impact factor:   6.531


  3 in total

1.  Extension of cervical screening intervals with primary human papillomavirus testing: observational study of English screening pilot data.

Authors:  Matejka Rebolj; Kate Cuschieri; Christopher S Mathews; Francesca Pesola; Karin Denton; Henry Kitchener
Journal:  BMJ       Date:  2022-05-31

2.  Clinical relevance of partial HPV16/18 genotyping in stratifying HPV-positive women attending routine cervical cancer screening: a population-based cohort study.

Authors:  S Gori; J Battagello; D Gustinucci; C Campari; M Zorzi; H Frayle; B Passamonti; G Sartori; S Bulletti; C Fodero; E Cesarini; R Faggiano; A Del Mistro
Journal:  BJOG       Date:  2021-01-12       Impact factor: 6.531

3.  Human papillomavirus-based screening at extended intervals missed fewer cervical precancers than cytology in the HPV For Cervical Cancer (HPV FOCAL) trial.

Authors:  Anna Gottschlich; Lovedeep Gondara; Laurie W Smith; Darrel Cook; Ruth Elwood Martin; Marette Lee; Stuart Peacock; Lily Proctor; Gavin Stuart; Mel Krajden; Eduardo L Franco; Dirk van Niekerk; Gina Ogilvie
Journal:  Int J Cancer       Date:  2022-05-10       Impact factor: 7.316

  3 in total

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