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Meta-Analysis
. 2009 May;35(3):210-20.
doi: 10.1016/j.ctrv.2008.10.005. Epub 2009 Mar 3.

p16(INK4a) immunostaining in cytological and histological specimens from the uterine cervix: a systematic review and meta-analysis

Affiliations
Meta-Analysis

p16(INK4a) immunostaining in cytological and histological specimens from the uterine cervix: a systematic review and meta-analysis

I Tsoumpou et al. Cancer Treat Rev. 2009 May.

Abstract

Background: P16(INK4a) is a biomarker for transforming HPV infections that could act as an adjunct to current cytological and histological assessment of cervical smears and biopsies, allowing the identification of those women with ambiguous results that require referral to colposcopy and potentially treatment.

Material and methods: We conducted a systematic review of all studies that evaluated the use of p16(INK4a) in cytological or histological specimens from the uterine cervix. We also estimated the mean proportion of samples that were positive for p16(INK4a) in cytology and histology, stratified by the grade of the lesion.

Results: Sixty-one studies were included. The proportion of cervical smears overexpressing p16(INK4a) increased with the severity of cytological abnormality. Among normal smears, only 12% (95% CI: 7-17%) were positive for the biomarker compared to 45% of ASCUS and LSIL (95% CI: 35-54% and 37-57%, respectively) and 89% of HSIL smears (95% CI: 84-95%). Similarly, in histology only 2% of normal biopsies (95% CI: 0.4-30%) and 38% of CIN1 (95% CI: 23-53%) showed diffuse staining for p16(INK4a) compared to 68% of CIN2 (95% CI: 44-92%) and 82% of CIN3 (95% CI: 72-92%).

Conclusion: Although there is good evidence that p16(INK4a) immunostaining correlates with the severity of cytological/histological abnormalities, the reproducibility is limited due to insufficiently standardized interpretation of the immunostaining. Therefore, a consensus needs to be reached regarding the evaluation of p16(INK4a) staining and the biomarker needs to be assessed in various clinical settings addressing specific clinical questions.

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Figures

Figure 1
Figure 1. Flowchart of study selection
Figure 2
Figure 2. Meta-analysis of the proportion of samples stained positive for p16 per cytological category
WNL: within normal limits, ASCUS: atypical cells of undetermined significance, LSIL: low-grade intraepithelial lesion, HSIL: high-grade squamous intraepithelial lesion
Figure 3
Figure 3. Meta-analysis of the proportion of biopsies stained positive for p16 per grade of cervical lesion
CIN: cervical intraepithelial neoplasia

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