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The Interpretive Variability of Cervical Biopsies and Its Relationship to HPV Status

Diagnostic interpretation of a cervical biopsy is a key element in the decision to treat or not to treat a woman with an abnormal screening test. This study assesses the variability of these diagnostic interpretations on a population basis using the New Mexico HPV Pap Registry database. An experienc...

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Autores principales: Stoler, Mark H., Ronnett, Brigitte M., Joste, Nancy E., Hunt, William C., Cuzick, Jack, Wheeler, Cosette M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Raven Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4428379/
https://www.ncbi.nlm.nih.gov/pubmed/25602796
http://dx.doi.org/10.1097/PAS.0000000000000381
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author Stoler, Mark H.
Ronnett, Brigitte M.
Joste, Nancy E.
Hunt, William C.
Cuzick, Jack
Wheeler, Cosette M.
author_facet Stoler, Mark H.
Ronnett, Brigitte M.
Joste, Nancy E.
Hunt, William C.
Cuzick, Jack
Wheeler, Cosette M.
author_sort Stoler, Mark H.
collection PubMed
description Diagnostic interpretation of a cervical biopsy is a key element in the decision to treat or not to treat a woman with an abnormal screening test. This study assesses the variability of these diagnostic interpretations on a population basis using the New Mexico HPV Pap Registry database. An experienced panel of gynecologic pathologists reviewed a stratified random sample of 6272 biopsies, which was then extrapolated to the entire population of 21,297 biopsies read by the community pathologists. Diagnoses by the community and panel pathologists were compared, and paired diagnoses were correlated with positivity for human papillomavirus 16 (HPV16) and any high-risk HPV as objective measures of progressive potential. Panel agreement with the community diagnosis was 38.2% for cervical intraepithelial neoplasia grade 1 (CIN1), 38.0% for CIN grade 2 (CIN2), 68.0% for CIN grade 3 (CIN3), and 70.6% for cancer. The κ value was 0.46 overall but higher for dichotomous categorization based on CIN2 or CIN3 cutoff points (0.68 and 0.67, respectively). On a population basis, there were fewer CIN1 and more negative diagnoses in the panel review but similar proportions of CIN2 and CIN3. HPV16 and high-risk HPV positivity increased with disease severity, but panel review did not improve the correlation of higher-grade disease with these objective measures. In this population-based study of the variability in cervical diagnoses, we noted significant variability in the community and panel diagnoses, especially for CIN2, the threshold for excisional treatment. New biomarkers are needed to more accurately stratify precursor lesions according to their malignant potential.
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spelling pubmed-44283792015-05-15 The Interpretive Variability of Cervical Biopsies and Its Relationship to HPV Status Stoler, Mark H. Ronnett, Brigitte M. Joste, Nancy E. Hunt, William C. Cuzick, Jack Wheeler, Cosette M. Am J Surg Pathol Original Articles Diagnostic interpretation of a cervical biopsy is a key element in the decision to treat or not to treat a woman with an abnormal screening test. This study assesses the variability of these diagnostic interpretations on a population basis using the New Mexico HPV Pap Registry database. An experienced panel of gynecologic pathologists reviewed a stratified random sample of 6272 biopsies, which was then extrapolated to the entire population of 21,297 biopsies read by the community pathologists. Diagnoses by the community and panel pathologists were compared, and paired diagnoses were correlated with positivity for human papillomavirus 16 (HPV16) and any high-risk HPV as objective measures of progressive potential. Panel agreement with the community diagnosis was 38.2% for cervical intraepithelial neoplasia grade 1 (CIN1), 38.0% for CIN grade 2 (CIN2), 68.0% for CIN grade 3 (CIN3), and 70.6% for cancer. The κ value was 0.46 overall but higher for dichotomous categorization based on CIN2 or CIN3 cutoff points (0.68 and 0.67, respectively). On a population basis, there were fewer CIN1 and more negative diagnoses in the panel review but similar proportions of CIN2 and CIN3. HPV16 and high-risk HPV positivity increased with disease severity, but panel review did not improve the correlation of higher-grade disease with these objective measures. In this population-based study of the variability in cervical diagnoses, we noted significant variability in the community and panel diagnoses, especially for CIN2, the threshold for excisional treatment. New biomarkers are needed to more accurately stratify precursor lesions according to their malignant potential. Raven Press 2015-06 2015-05-13 /pmc/articles/PMC4428379/ /pubmed/25602796 http://dx.doi.org/10.1097/PAS.0000000000000381 Text en Copyright © 2015 Wolters Kluwer Health, Inc. All rights reserved. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially. http://creativecommons.org/licenses/by-nc-nd/4.0.
spellingShingle Original Articles
Stoler, Mark H.
Ronnett, Brigitte M.
Joste, Nancy E.
Hunt, William C.
Cuzick, Jack
Wheeler, Cosette M.
The Interpretive Variability of Cervical Biopsies and Its Relationship to HPV Status
title The Interpretive Variability of Cervical Biopsies and Its Relationship to HPV Status
title_full The Interpretive Variability of Cervical Biopsies and Its Relationship to HPV Status
title_fullStr The Interpretive Variability of Cervical Biopsies and Its Relationship to HPV Status
title_full_unstemmed The Interpretive Variability of Cervical Biopsies and Its Relationship to HPV Status
title_short The Interpretive Variability of Cervical Biopsies and Its Relationship to HPV Status
title_sort interpretive variability of cervical biopsies and its relationship to hpv status
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4428379/
https://www.ncbi.nlm.nih.gov/pubmed/25602796
http://dx.doi.org/10.1097/PAS.0000000000000381
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