HPV 16/18 E7 oncoprotein detection as a promising triage strategy for HPV 16/18‐positive patients: A prospective multicenter study with a 2‐year follow up

Author:

Cao Yang1,Xiao Xiaoping1,Liang Dandan1,Lu Ye2,Liu Chongdong3,Li Hua3,Wang Wei1,Yang Junjun1,Wang Jinhui1,Li Yan1,Li Caijuan1,Guan Ruoli1,Zhang Dai2,Bi Hui2,Zhang Lei2,Qu Hong3,Xu Tao4,Zhang Ying5,Wang Jin6,Song Shuhui7,Shi Honghui1ORCID

Affiliation:

1. National Clinical Research Center for Obstetric & Gynecologic Diseases, Department of Obstetrics and Gynecology, Peking Union Medical College Hospital Chinese Academy of Medical Sciences & Peking Union Medical College Beijing China

2. Department of Obstetrics and Gynecology Peking University First Hospital Beijing China

3. Department of Obstetrics and Gynecology, Beijing Chao‐Yang Hospital Capital Medical University Beijing China

4. Institute of Basic Medical Sciences, Peking Union Medical College Chinese Academy of Medical Sciences Beijing China

5. Department of Nuclear Medicine, Peking Union Medical College Hospital Chinese Academy of Medical Sciences & Peking Union Medical College Beijing China

6. Department of Endocrinology, Peking Union Medical College Hospital Chinese Academy of Medical Sciences & Peking Union Medical College Beijing China

7. FAMID Biomedical Technology (Tianjin) Co., Ltd. Tianjin China

Abstract

AbstractObjectiveTo explore the effectiveness of HPV 16/18 E7 oncoprotein in detecting high‐grade cervical intraepithelial neoplasia (CIN) and predicting disease outcomes in HPV 16/18‐positive patients.MethodsThe present study was a cross‐sectional study with a 2‐year follow up. We collected 915 cervical exfoliated cell samples from patients who tested positive for HPV 16/18 in gynecologic clinics of three tertiary hospitals in Beijing from March 2021 to October 2022 for HPV 16/18 E7 oncoprotein testing. Subsequently, 2‐year follow up of 408 patients with baseline histologic CIN1 or below were used to investigate the predictive role of HPV 16/18 E7 oncoprotein in determining HPV persistent infection and disease progression.ResultsThe positivity rate of the HPV 16/18 E7 oncoprotein assay was 42.06% (249/592) in the inflammation/CIN 1 group and 85.45% (277/324) in the CIN2+ group. For CIN2+ detection, using the HPV 16/18 E7 oncoprotein assay combined with HPV 16/18 testing, the sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) were 85.45%, 57.94%, 52.57%, and 87.95%, respectively. During the 2‐year follow up, the sensitivity, specificity, PPV, and NPV for predicting persistent HPV infection were 48.44%, 58.21%, 34.64%, and 71.18% in the baseline inflammation and CIN1 group.ConclusionsAs a triage method for high‐grade CIN screening in HPV 16/18‐positive patients, HPV 16/18 E7 oncoprotein demonstrated a relatively high NPV, making it suitable for clinical use in triaging HPV 16/18‐positive cases and potentially reducing the colposcopic referral rate. HPV 16/18 E7 oncoprotein exhibited a preferably predictive value in determining HPV infection outcomes and disease progression.

Publisher

Wiley

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