ABSTRACT
Objective: This study aimed to evaluate p16 expression and its clinical utility in cervical biopsies from women who tested positive for high-risk human papillomavirus (HPV) in a real-world screening program, assessing its correlation with HPV genotype, lesion grade, clinical management, and diagnostic upgrading.
Methods: We conducted a diagnostic test study nested within the first round (2017- 2022) of a population-based HPV DNA screening program in a Brazilian municipality. Women who tested positive for HPV were referred for colposcopy, and those who underwent cervical biopsy with p16(INK4a) immunohistochemistry were included. We analyzed age, HPV results, biopsy diagnoses, p16 status, procedures, and clinical outcomes using the χ2 test or Fisher exact test and logistic regression (p < .05).
Results: Among 696 biopsies, 48.4% were p16-positive. Positivity increased with lesion severity, from 14.3% in negative biopsies to 80.0% in cervical intra-epithelial neoplasia grade 2 and 95.1% in cervical intra-epithelial neoplasia grade 3/adenocarcinoma in situ (p <.001). No significant association was found between p16 and specific HPV genotypes (43·4%-60%), although 73% of p16-positive carcinomas were linked to HPV16/18. Excisional treatment was performed in 61.7% of p16-positive cases versus 7.5% of p16-negative cases (p < .001). Cervical intra-epithelial neoplasia grade 2 or worse was diagnosed in 69.4% of p16-positive cases (p < .001), with diagnostic upgrading 7 times more frequent than in p16-negative cases (19.9% vs 2.8%; p < .001). p16 showed a positive predictive value of 69% and a negative predictive value of 90% for cervical intra-epithelial neoplasia grade 2 or worse detection, reaching 91.6% in the non-HPV16/18 sub-group. The regression analysis confirmed p16 expression with 20-fold higher odds for significative cervical lesions (odds ratio 20.2, 95% confidence interval 13.3 to 30.6, p < .001).
Conclusions: Systematic p16 assessment in population-based screening improves risk stratification, diagnostic accuracy, and treatment allocation. These findings support integrating p16 into cervical cancer prevention strategies, particularly, in resourcelimited settings where optimizing diagnostic precision and treatment balance is crucial.
Document: IJGC_p16_PUBLICADO_31DEZ2025
