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. 2019 Sep;134(3):452-462.
doi: 10.1097/AOG.0000000000003409.

Human Papillomavirus Genotyping Compared With a Qualitative High-Risk Human Papillomavirus Test After Treatment of High-Grade Cervical Intraepithelial Neoplasia: A Systematic Review

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Human Papillomavirus Genotyping Compared With a Qualitative High-Risk Human Papillomavirus Test After Treatment of High-Grade Cervical Intraepithelial Neoplasia: A Systematic Review

Fabio Bottari et al. Obstet Gynecol. 2019 Sep.

Abstract

Objective: To systematically examine human papillomavirus (HPV) genotyping compared with qualitative high-risk HPV result during follow-up after treatment of high-grade cervical intraepithelial neoplasia (CIN), for risk estimation of posttreatment high-grade CIN.

Data sources: MEDLINE, Cochrane, and ClinicalTrials.gov were searched from January 2000 to April 2019 for prospective studies of women and retrospective studies of residual specimens from women, tested using HPV assays with genotype reporting.

Methods of study selection: The primary outcome was posttreatment high-grade CIN after treatment of high-grade CIN. Risk of bias (individual study quality) was evaluated with a modified Newcastle-Ottawa Scale. Overall quality of evidence for the risk estimate outcomes was evaluated using modified GRADE methodology for observational diagnostic studies.

Tabulation, integration, and results: Of the 233 identified abstracts, 33 full-text articles were retrieved, and seven studies were included in the synthesis. The risk of bias was deemed to be low. Either a positive qualitative HPV test result or a positive test result for the same genotype that was present pretreatment have a sensitivity for predicting posttreatment high-grade CIN that approaches 100%. However, the positive predictive value (PPV) for the same genotype result pretreatment and posttreatment (median 44.4%) is about double the PPV (median 22.2%) for qualitative HPV results. The PPV of a new HPV infection posttreatment approximates zero. Human papillomavirus genotyping discriminated risk of posttreatment high-grade CIN to a clinically significant degree for women after treatment procedures for high-grade CIN lesions, when same-genotype persistence was compared with new genotype infection.

Conclusion: There is moderately high-quality evidence to support the improved clinical utility of HPV genotyping compared with qualitative HPV positivity to follow-up after treatment of high-grade CIN.

Systematic review registration: PROSPERO: CRD42018091095.

Funding source: Becton, Dickinson and Company, BD Life Sciences-Diagnostic Systems.

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Figures

Fig. 1.
Fig. 1.. The PRISMA (Preferred Reporting of Items for Systematic Reviews) flow diagram detailing the search and selection process. HPV, human papillomavirus.
Bottari. Human Papillomavirus Genotyping After High-Grade CIN Treatment. Obstet Gynecol 2019.
Fig. 2.
Fig. 2.. Receiver operating characteristics curves (sensitivity against 1-specificity) for three posttreatment human papillomavirus (HPV) results. Median values from the three screening strategies for sensitivity and specificity values obtained from the seven included studies: blue circle point values and hashed line represent qualitative HPV-positive, orange circle point values and hashed line represent same-genotype persistence, and orange triangle point values and orange dotted lines represent new HPV genotype infection posttreatment. The overall screening group (from the seven studies) median values for sensitive and 1-specificity are plotted as single points and represent qualitative HPV-positive (blue diamond), same-genotype persistence (orange diamond) and new infection (white diamond). Receiver operating characteristics analysis revealed area under the curve values close to 1 for qualitative HPV and same-genotype persistence; the new infection area under the curve value was 0.24.
Bottari. Human Papillomavirus Genotyping After High-Grade CIN Treatment. Obstet Gynecol 2019.

Comment in

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