Accuracy of high-risk HPV DNA PCR, p16


Journal

BMC infectious diseases
ISSN: 1471-2334
Titre abrégé: BMC Infect Dis
Pays: England
ID NLM: 100968551

Informations de publication

Date de publication:
06 Aug 2022
Historique:
received: 22 10 2021
accepted: 08 07 2022
entrez: 6 8 2022
pubmed: 7 8 2022
medline: 10 8 2022
Statut: epublish

Résumé

The incidence of high-risk human papillomavirus (hrHPV)-driven head and neck squamous cell carcinoma, in particular oropharyngeal cancers (OPC), is increasing in high-resource countries. Patients with HPV-induced cancer respond better to treatment and consequently have lower case-fatality rates than patients with HPV-unrelated OPC. These considerations highlight the importance of reliable and accurate markers to diagnose truly HPV-induced OPC. The accuracy of three possible test strategies, i.e. (a) hrHPV DNA PCR (DNA), (b) p16 Ninety-nine OPC patients were included, for which the positivity rates were 36.4%, 34.0% and 28.9% for DNA, p16 and mRNA, respectively. Ninety-five OPC patients had valid test results for all three tests (DNA, p16 and mRNA). Using mRNA status as the reference, DNA testing showed 100% (28/28) sensitivity, and 92.5% (62/67) specificity for the detection of HPV-driven cancer. p16 was 96.4% (27/28) sensitive and equally specific (92.5%; 62/67). The sensitivity and specificity of combined p16 + DNA testing was 96.4% (27/28) and 97.0% (65/67), respectively. In this series, p16 alone and combined p16 + DNA missed 1 in 28 HPV driven cancers, but p16 alone misclassified 5 in 67 non-HPV driven as positive, whereas combined testing would misclassify only 2 in 67. Single hrHPV DNA PCR and p16

Sections du résumé

BACKGROUND BACKGROUND
The incidence of high-risk human papillomavirus (hrHPV)-driven head and neck squamous cell carcinoma, in particular oropharyngeal cancers (OPC), is increasing in high-resource countries. Patients with HPV-induced cancer respond better to treatment and consequently have lower case-fatality rates than patients with HPV-unrelated OPC. These considerations highlight the importance of reliable and accurate markers to diagnose truly HPV-induced OPC.
METHODS METHODS
The accuracy of three possible test strategies, i.e. (a) hrHPV DNA PCR (DNA), (b) p16
RESULTS RESULTS
Ninety-nine OPC patients were included, for which the positivity rates were 36.4%, 34.0% and 28.9% for DNA, p16 and mRNA, respectively. Ninety-five OPC patients had valid test results for all three tests (DNA, p16 and mRNA). Using mRNA status as the reference, DNA testing showed 100% (28/28) sensitivity, and 92.5% (62/67) specificity for the detection of HPV-driven cancer. p16 was 96.4% (27/28) sensitive and equally specific (92.5%; 62/67). The sensitivity and specificity of combined p16 + DNA testing was 96.4% (27/28) and 97.0% (65/67), respectively. In this series, p16 alone and combined p16 + DNA missed 1 in 28 HPV driven cancers, but p16 alone misclassified 5 in 67 non-HPV driven as positive, whereas combined testing would misclassify only 2 in 67.
CONCLUSIONS CONCLUSIONS
Single hrHPV DNA PCR and p16

Identifiants

pubmed: 35933382
doi: 10.1186/s12879-022-07654-2
pii: 10.1186/s12879-022-07654-2
pmc: PMC9357318
doi:

Substances chimiques

Cyclin-Dependent Kinase Inhibitor p16 0
DNA, Viral 0
RNA, Messenger 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

676

Subventions

Organisme : European Commission
ID : FP7-HEALTH-2011-282562
Organisme : Horizon 2020 Framework Programme for Research and Innovation of the European Commission
ID : 847845
Organisme : the Belgian Foundation Against Cancer
ID : IHUVACC

Investigateurs

Christine Carreira (C)
Sandrine McKay-Chopin (S)
Rudrapatna S Jayshree (RS)
Kortikere S Sabitha (KS)
Ashok M Shenoy (AM)
Alfredo Zito (A)
Fausto Chiesa (F)
Marta Tagliabue (M)
Mohssen Ansarin (M)
Subha Sankaran (S)
Christel Herold-Mende (C)
Gerhard Dyckhoff (G)
George Mosialos (G)
Heiner Boeing (H)
Xavier Castellsagué (X)
Silvia de Sanjosé (S)
Marisa Mena (M)
Francesc Xavier Bosch (FX)
Laia Alemany (L)
Pulikottil Okkuru Esmy (PO)
Manavalan Vijayakumar (M)
Aruna S Chiwate (AS)
Ranjit V Thorat (RV)
Girish G Hublikar (GG)
Shashikant S Lakshetti (SS)
Bhagwan M Nene (BM)
Amal Ch Kataki (AC)
Ashok Kumar Das (AK)
Kunnambath Ramadas (K)
Thara Somanathan (T)

Informations de copyright

© 2022. The Author(s).

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Auteurs

Cindy Simoens (C)

Unit of Cancer Epidemiology, Belgian Cancer Centre, Sciensano, Juliette Wytsmanstraat 14, 1050, Brussels, Belgium. cindy.simoens@sciensano.be.
AMBIOR, Laboratory for Cell Biology & Histology, University of Antwerp, Antwerp, Belgium. cindy.simoens@sciensano.be.

Tarik Gheit (T)

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

Ruediger Ridder (R)

Roche Diagnostics GmbH, Mannheim, Germany.
Ventana Medical Systems, Inc. (Roche Diagnostics Solutions), Tucson, AZ, USA.

Ivana Gorbaslieva (I)

AMBIOR, Laboratory for Cell Biology & Histology, University of Antwerp, Antwerp, Belgium.

Dana Holzinger (D)

Infections and Cancer Epidemiology, Research Program Infection, Inflammation and Cancer, Deutsches Krebsforschungszentrum, Heidelberg, Germany.

Eric Lucas (E)

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

Susanne Rehm (S)

Roche Diagnostics GmbH, Mannheim, Germany.

Peter Vermeulen (P)

Laboratory for Pathological Anatomy, Sint Augustinus Hospital, GZA, Antwerp, Belgium.

Martin Lammens (M)

Department of Pathology, Antwerp University Hospital, Edegem, Belgium.
Center for Oncological Research, Faculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium.

Olivier M Vanderveken (OM)

Department of Otorhinolaryngology, Head and Neck Surgery, Antwerp University Hospital, Edegem, Belgium.
Department of Translational Neurosciences, Faculty of Medicine and Health Sciences, University of Antwerp, Antwerp, Belgium.

Rekha Vijay Kumar (RV)

Kidwai Memorial Institute of Oncology, Bangalore, Karnataka, 560029, India.

Nitin Gangane (N)

Mahatma Gandhi Institute of Medical Sciences, Sevagram, Wardha, Maharashtra State, 442102, India.

Alessandro Caniglia (A)

IRCCS Istituto Tumori "Giovanni Paolo II", Bari, Italy.

Fausto Maffini (F)

Division of Pathology, IEO, European Institute of Oncology IRCCS, Milan, Italy.

Maria Belén Lloveras Rubio (MBL)

Hospital del Mar, Parc de Salut Mar, Pg/Marítim 25-29, 08003, Barcelona, Spain.

Devasena Anantharaman (D)

Rajiv Gandhi Centre for Biotechnology, Poojappura, Thiruvananthapuram, Kerala, 695014, India.

Susanna Chiocca (S)

Department of Experimental Oncology, IEO, European Institute of Oncology IRCCS, Milan, Italy.

Paul Brennan (P)

Genomic Epidemiology Branch, International Agency for Research On Cancer (IARC), Lyon, France.

Madhavan Radhakrishna Pillai (MR)

Rajiv Gandhi Centre for Biotechnology, Poojappura, Thiruvananthapuram, Kerala, 695014, India.

Rengaswamy Sankaranarayanan (R)

Research Triangle Institute (RTI) International India, New Delhi, India.

Johannes Bogers (J)

AMBIOR, Laboratory for Cell Biology & Histology, University of Antwerp, Antwerp, Belgium.

Michael Pawlita (M)

Infections and Cancer Epidemiology, Research Program Infection, Inflammation and Cancer, Deutsches Krebsforschungszentrum, Heidelberg, Germany.

Massimo Tommasino (M)

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

Marc Arbyn (M)

Unit of Cancer Epidemiology, Belgian Cancer Centre, Sciensano, Juliette Wytsmanstraat 14, 1050, Brussels, Belgium. marc.arbyn@sciensano.be.

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