Accuracy of HPV E6/E7 oncoprotein tests to detect high-grade cervical lesions: a systematic literature review and meta-analysis.


Journal

British journal of cancer
ISSN: 1532-1827
Titre abrégé: Br J Cancer
Pays: England
ID NLM: 0370635

Informations de publication

Date de publication:
16 Nov 2023
Historique:
received: 15 05 2023
accepted: 31 10 2023
revised: 24 10 2023
medline: 17 11 2023
pubmed: 17 11 2023
entrez: 17 11 2023
Statut: aheadofprint

Résumé

Cervical carcinogenesis is mediated by the HPV-E6 and E7 oncoproteins, considered as biomarkers usable in managing screen-positive women. We conducted a systematic review and meta-analysis assessing the accuracy of HPV-E6/E7-oncoprotein tests to detect underlying cervical-precancer and cancer. We included studies reporting data on oncoprotein test accuracy detecting cervical intraepithelial neoplasia grade 3 or worse. Random effects logistic regression models were applied for pooling absolute and relative accuracy. Twenty-two studies were included. Sensitivity and specificity estimates ranged from 54.2% (95%CI: 45.2-63.0) to 69.5% (95%CI:60.8-76.9) and from 82.8% (95%CI: 50.4-95.8) to 99.1 (95%CI: 98.8-99.3), respectively in the population irrespective of HPV status. Higher sensitivity estimates ranging from 60.8% (95%CI: 49.6-70.9) to 75.5% (95%CI: 71.7-78.9) but lower specificity estimates ranging from 83.7% (95%CI: 76.1-89.3) to 92.1% (95%CI: 88.5-94.6) were observed in studies enrolling high-risk-HPV-positive women. Studies recruiting only HIV-positive women showed a pooled sensitivity of 46.9% (95%CI: 30.6-63.9) with a specificity of 98.0% (95%CI: 96.8-98.7). The high specificity of oncoprotein tests supports its use for triaging HPV-positive women. However, oncoprotein-negative women would not be recommended to undertake routine screening, requiring further follow-up. Large-scale and longitudinal studies are needed to further investigate the role of E6/E7-oncoprotein detection in predicting the risk of developing cervical pre-cancer and cancer.

Sections du résumé

BACKGROUND BACKGROUND
Cervical carcinogenesis is mediated by the HPV-E6 and E7 oncoproteins, considered as biomarkers usable in managing screen-positive women.
METHODS METHODS
We conducted a systematic review and meta-analysis assessing the accuracy of HPV-E6/E7-oncoprotein tests to detect underlying cervical-precancer and cancer. We included studies reporting data on oncoprotein test accuracy detecting cervical intraepithelial neoplasia grade 3 or worse. Random effects logistic regression models were applied for pooling absolute and relative accuracy.
RESULTS RESULTS
Twenty-two studies were included. Sensitivity and specificity estimates ranged from 54.2% (95%CI: 45.2-63.0) to 69.5% (95%CI:60.8-76.9) and from 82.8% (95%CI: 50.4-95.8) to 99.1 (95%CI: 98.8-99.3), respectively in the population irrespective of HPV status. Higher sensitivity estimates ranging from 60.8% (95%CI: 49.6-70.9) to 75.5% (95%CI: 71.7-78.9) but lower specificity estimates ranging from 83.7% (95%CI: 76.1-89.3) to 92.1% (95%CI: 88.5-94.6) were observed in studies enrolling high-risk-HPV-positive women. Studies recruiting only HIV-positive women showed a pooled sensitivity of 46.9% (95%CI: 30.6-63.9) with a specificity of 98.0% (95%CI: 96.8-98.7).
CONCLUSIONS CONCLUSIONS
The high specificity of oncoprotein tests supports its use for triaging HPV-positive women. However, oncoprotein-negative women would not be recommended to undertake routine screening, requiring further follow-up. Large-scale and longitudinal studies are needed to further investigate the role of E6/E7-oncoprotein detection in predicting the risk of developing cervical pre-cancer and cancer.

Identifiants

pubmed: 37973957
doi: 10.1038/s41416-023-02490-w
pii: 10.1038/s41416-023-02490-w
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : World Health Organization
ID : 001
Pays : International

Informations de copyright

© 2023. The Author(s).

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Auteurs

Laura Downham (L)

Early Detection, Prevention and Infections Branch, International Agency for Research on Cancer, Lyon, France. downhaml@iarc.who.int.

Iman Jaafar (I)

Department of Cancer Epidemiology, Scientific Institute of Public Health, Brussels, Belgium.

Mary Luz Rol (ML)

Early Detection, Prevention and Infections Branch, International Agency for Research on Cancer, Lyon, France.

Victoria Nyawira Nyaga (V)

Department of Cancer Epidemiology, Scientific Institute of Public Health, Brussels, Belgium.

Joan Valls (J)

Early Detection, Prevention and Infections Branch, International Agency for Research on Cancer, Lyon, France.
Cancer Epidemiology Research Program, Catalan Institute of Oncology (ICO), Idibell, Barcelona, Spain.

Armando Baena (A)

Early Detection, Prevention and Infections Branch, International Agency for Research on Cancer, Lyon, France.

Li Zhang (L)

Early Detection, Prevention and Infections Branch, International Agency for Research on Cancer, Lyon, France.

Marc J Gunter (MJ)

Department of Epidemiology and Biostatistics, School of Public Health, Imperial College London, London, UK.
Nutrition and Metabolism Branch, International Agency for Research on Cancer, Lyon, France.

Marc Arbyn (M)

Department of Cancer Epidemiology, Scientific Institute of Public Health, Brussels, Belgium.
Department of Human Structure and Repair, Faculty of Medicine and Health Sciences, Ghent University, Ghent, Belgium.

Maribel Almonte (M)

Early Detection, Prevention and Infections Branch, International Agency for Research on Cancer, Lyon, France.
Department of Non-Communicable Diseases, World Health Organisation, Geneva, France.

Classifications MeSH