Objective: To evaluate partial HPV16/18 genotyping as a possible biomarker to select women attending HPV-based cervical cancer screening at higher risk to be referred to colposcopy.

Design: Population-based cohort study.

Setting: Organised cervical cancer screening programmes (Italy).

Population: Women with high-risk HPV infection (period: 2015-2019).

Methods: We analysed the association between partial HPV16/18 genotyping, cytology triage and histologically confirmed diagnosis of high-grade cervical intraepithelial neoplasia (CIN3 ) lesions.

Main Outcome Measures: Detection rate (DR) and positive predictive value (PPV) for histologically confirmed CIN3 (any episode in the 2 years after baseline); sensitivity for CIN3 and number of colposcopies needed for lesion detection.

Results: The study included 145 437 women screened with HPV testing by the clinically validated COBAS 4800 HPV assay (Roche). Overall, 9601 (6.6%) women were HPV at baseline; HPV16 and HPV18 were present in 1865 and 594 samples, respectively. The cumulative (baseline plus 1-year repeat) cytology positivity was 42.8% and high-grade cytology was significantly higher (P < 0.0001) among women with HPV16 infection at baseline (15.2%). The cumulative CIN3 DR for women with HPV16, HPV18 and other HPV-type infections was 9.8%, 3.4% and 1.8%, respectively.

Conclusions: Partial HPV16 genotyping may play a role in triage, whereas HPV18 seems to behave much more similarly to the other HPV types and does not provide additional stratification. HPV16 genotyping combined with high-grade cytology can be envisaged as a triage biomarker in cervical screening to maximise CIN3 detection while minimising colposcopy at baseline or 1-year repeat.

Tweetable Abstract: HPV16 genotyping combined with high-grade cytology can be used as triage biomarker for CIN3 in HPV-positive women.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8248328PMC
http://dx.doi.org/10.1111/1471-0528.16631DOI Listing

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