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Performance of HPV E4 and p16(INK4a) biomarkers in predicting regression of cervical intraepithelial neoplasia grade 2 (CIN2): protocol for a historical cohort study

INTRODUCTION: Cervical intraepithelial neoplasia grade 2 (CIN2) represents a spectrum of lesions with variable progression and regression. Pathological diagnosis of CIN2 is subjective and poorly reproducible. Accurate diagnosis and identification of different patterns of CIN2 related to outcome are...

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Autores principales: Damgaard, Rikke Kamp, Jenkins, David, de Koning, Maurits NC, Quint, Wim GV, Stoler, Mark H, Doorbar, John, Kahlert, Johnny, Gravitt, Patti E, Steiniche, Torben, Petersen, Lone Kjeld, Hammer, Anne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9260811/
https://www.ncbi.nlm.nih.gov/pubmed/35793925
http://dx.doi.org/10.1136/bmjopen-2021-059593
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author Damgaard, Rikke Kamp
Jenkins, David
de Koning, Maurits NC
Quint, Wim GV
Stoler, Mark H
Doorbar, John
Kahlert, Johnny
Gravitt, Patti E
Steiniche, Torben
Petersen, Lone Kjeld
Hammer, Anne
author_facet Damgaard, Rikke Kamp
Jenkins, David
de Koning, Maurits NC
Quint, Wim GV
Stoler, Mark H
Doorbar, John
Kahlert, Johnny
Gravitt, Patti E
Steiniche, Torben
Petersen, Lone Kjeld
Hammer, Anne
author_sort Damgaard, Rikke Kamp
collection PubMed
description INTRODUCTION: Cervical intraepithelial neoplasia grade 2 (CIN2) represents a spectrum of lesions with variable progression and regression. Pathological diagnosis of CIN2 is subjective and poorly reproducible. Accurate diagnosis and identification of different patterns of CIN2 related to outcome are essential to reduce the risks of overtreatment or undertreatment. It is important to explore novel methods for risk stratification of CIN2 to enable targeted treatment of women at high risk of progression or persistent disease and follow-up of women at low risk. The combination of the novel biomarker human papillomavirus (HPV) E4 with p16(INK4a) targets steps in the transition from a productive oncogenic HPV infection (CIN1) to a transformed lesion (CIN3) within CIN2. Previous cross-sectional studies suggest that HPV E4 combined with p16(INK4a) may be valuable for risk assessment of CIN2. However, data on HPV E4/p16(INK4a) as a predictor for CIN2 regression is lacking. METHODS AND ANALYSIS: We will conduct a historical cohort study including 500 women aged 23–40 years with a first CIN2 diagnosis in Aarhus, Denmark during 2000–2010. Women will be eligible if they have undergone active surveillance and have no previous record of hysterectomy, cone biopsy, and CIN2 or worse. Women will be randomly selected through the Danish Pathology Databank. Tissue samples from women included will be sectioned for p16(INK4a) and HPV E4 immunohistochemical staining in addition to conventional hematoxylin and eosin (H&E) staining. A positive result will be defined as HPV E4 positive. Through the Danish Pathology Databank, we will collect results on all subsequent cervical biopsies. Regression will be used as the primary outcome. ETHICS AND DISSEMINATION: The study has been approved by the Ethical Committee in Central Denmark Region (1-10-72-60-20) and registered at the Faculty of Health, Aarhus University. Results will be published in a peer-reviewed journal and presented at scientific meetings. TRIAL REGISTRATION NUMBER: NCT05049252.
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spelling pubmed-92608112022-07-25 Performance of HPV E4 and p16(INK4a) biomarkers in predicting regression of cervical intraepithelial neoplasia grade 2 (CIN2): protocol for a historical cohort study Damgaard, Rikke Kamp Jenkins, David de Koning, Maurits NC Quint, Wim GV Stoler, Mark H Doorbar, John Kahlert, Johnny Gravitt, Patti E Steiniche, Torben Petersen, Lone Kjeld Hammer, Anne BMJ Open Obstetrics and Gynaecology INTRODUCTION: Cervical intraepithelial neoplasia grade 2 (CIN2) represents a spectrum of lesions with variable progression and regression. Pathological diagnosis of CIN2 is subjective and poorly reproducible. Accurate diagnosis and identification of different patterns of CIN2 related to outcome are essential to reduce the risks of overtreatment or undertreatment. It is important to explore novel methods for risk stratification of CIN2 to enable targeted treatment of women at high risk of progression or persistent disease and follow-up of women at low risk. The combination of the novel biomarker human papillomavirus (HPV) E4 with p16(INK4a) targets steps in the transition from a productive oncogenic HPV infection (CIN1) to a transformed lesion (CIN3) within CIN2. Previous cross-sectional studies suggest that HPV E4 combined with p16(INK4a) may be valuable for risk assessment of CIN2. However, data on HPV E4/p16(INK4a) as a predictor for CIN2 regression is lacking. METHODS AND ANALYSIS: We will conduct a historical cohort study including 500 women aged 23–40 years with a first CIN2 diagnosis in Aarhus, Denmark during 2000–2010. Women will be eligible if they have undergone active surveillance and have no previous record of hysterectomy, cone biopsy, and CIN2 or worse. Women will be randomly selected through the Danish Pathology Databank. Tissue samples from women included will be sectioned for p16(INK4a) and HPV E4 immunohistochemical staining in addition to conventional hematoxylin and eosin (H&E) staining. A positive result will be defined as HPV E4 positive. Through the Danish Pathology Databank, we will collect results on all subsequent cervical biopsies. Regression will be used as the primary outcome. ETHICS AND DISSEMINATION: The study has been approved by the Ethical Committee in Central Denmark Region (1-10-72-60-20) and registered at the Faculty of Health, Aarhus University. Results will be published in a peer-reviewed journal and presented at scientific meetings. TRIAL REGISTRATION NUMBER: NCT05049252. BMJ Publishing Group 2022-07-06 /pmc/articles/PMC9260811/ /pubmed/35793925 http://dx.doi.org/10.1136/bmjopen-2021-059593 Text en © Author(s) (or their employer(s)) 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Obstetrics and Gynaecology
Damgaard, Rikke Kamp
Jenkins, David
de Koning, Maurits NC
Quint, Wim GV
Stoler, Mark H
Doorbar, John
Kahlert, Johnny
Gravitt, Patti E
Steiniche, Torben
Petersen, Lone Kjeld
Hammer, Anne
Performance of HPV E4 and p16(INK4a) biomarkers in predicting regression of cervical intraepithelial neoplasia grade 2 (CIN2): protocol for a historical cohort study
title Performance of HPV E4 and p16(INK4a) biomarkers in predicting regression of cervical intraepithelial neoplasia grade 2 (CIN2): protocol for a historical cohort study
title_full Performance of HPV E4 and p16(INK4a) biomarkers in predicting regression of cervical intraepithelial neoplasia grade 2 (CIN2): protocol for a historical cohort study
title_fullStr Performance of HPV E4 and p16(INK4a) biomarkers in predicting regression of cervical intraepithelial neoplasia grade 2 (CIN2): protocol for a historical cohort study
title_full_unstemmed Performance of HPV E4 and p16(INK4a) biomarkers in predicting regression of cervical intraepithelial neoplasia grade 2 (CIN2): protocol for a historical cohort study
title_short Performance of HPV E4 and p16(INK4a) biomarkers in predicting regression of cervical intraepithelial neoplasia grade 2 (CIN2): protocol for a historical cohort study
title_sort performance of hpv e4 and p16(ink4a) biomarkers in predicting regression of cervical intraepithelial neoplasia grade 2 (cin2): protocol for a historical cohort study
topic Obstetrics and Gynaecology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9260811/
https://www.ncbi.nlm.nih.gov/pubmed/35793925
http://dx.doi.org/10.1136/bmjopen-2021-059593
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