Low-intensity cervical screening shows similar CIN2+ risk to high-intensity screening in HPV-vaccinated women
This randomized controlled trial in Finland evaluated cervical cancer screening frequency in women vaccinated against HPV16/18 as early adolescents (ages 12-15). A total of 5626 women were allocated at age 22 into either high-intensity (Arm A1) or low-intensity (Arm A2) cytology-based screening arms, with follow-up through age 28 (216 months).
The primary outcome was histopathologically confirmed cervical intraepithelial neoplasia grade 2 or worse (CIN2+). The occurrence of CIN2+ was 0.70% in the high-intensity arm and 0.66% in the low-intensity arm. The hazard ratio comparing low-intensity to high-intensity screening was 0.97 (95% confidence interval 0.50-1.88), indicating no statistically significant difference in risk. Secondary analyses showed the occurrence of vaccine-targeted HPV types 16/18 was reduced by up to 88% at age 28.
Safety and tolerability data were not reported. The study's key limitation is its specific population of women who received three doses of HPV16/18 vaccine as adolescents in Finland; results may not generalize to unvaccinated populations, those with different vaccination schedules, or other geographic settings. Funding and conflicts of interest were not reported.
For practice, this RCT provides evidence that in women vaccinated against HPV16/18 during early adolescence, less frequent cervical screening may not increase short-term risk of CIN2+ precursors through age 28. However, clinicians should recognize these findings are population-specific and do not yet support broad changes to screening guidelines for all women.