HPV detection and genotyping of head and neck cancer biopsies by molecular testing with regard to the new oropharyngeal squamous cell carcinoma classification based on HPV status

被引:12
作者
Veyer, David [1 ,2 ]
Wack, Maxine [2 ,3 ,4 ]
Grard, Ophelie [1 ,2 ]
Bonfils, Pierre [2 ,4 ,5 ]
Hans, Stephane [2 ,5 ,7 ]
Belec, Laurent [1 ,2 ,4 ]
Badoual, Cecile [2 ,4 ,6 ]
Pere, Helene [1 ,2 ,4 ]
机构
[1] Hop Europeen Georges Pompidou, Lab Virol, Paris, France
[2] AP HP, Paris, France
[3] Hop Europeen Georges Pompidou, Dept Informat Med Biostatist & Sante Publ, Paris, France
[4] Sorbonne Paris Cite, Univ Paris Descartes Paris 5, Fac Med Paris Descartes, Paris, France
[5] Hop Europeen Georges Pompidou, Serv ORL & Chirurg Cerv Faciale, Paris, France
[6] Hop Europeen Georges Pompidou, Lab Anatomo Cytopathol, Paris, France
[7] Univ Versailles St Quentin En Yvelines, UFR Simone Veil, Serv ORL & Chirurg Cerv Faciale, Hop Foch, Saint Quentin, France
关键词
Anyplex II HPV28 HPV genotyping assay; Inno-Lipa HPV Genotyping Extra II; HPV16 E6 viral load; HNSCC; FFPE biopsy; ANYPLEX II HPV28; HUMAN-PAPILLOMAVIRUS; ORAL-CAVITY; INNO-LIPA; ASSAYS; EPIDEMIOLOGY; EDITION; DNA;
D O I
10.1016/j.pathol.2019.02.002
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Recently, both the World Health Organization/International Agency for Research on Cancer (WHO/IARC) and the American Joint Committee on Cancer (AJCC) have classified oropharyngeal squamous cell carcinoma (OPSCC) on the basis of HPV status. For this purpose, the WHO/IARC recommended direct molecular HPV testing. In practice, formalin-fixed, paraffin-embedded (FFPE) biopsy specimens are frequently the only available samples. We herein compared in parallel two commercially available molecular assays that were first designed for cervical HPV detection and genotyping: Inno-Lipa HPV Genotyping Extra II (IL) and Anyplex II HPV28 (AP28). A total of 55 samples were tested. By IL assay, chosen as reference assay, 27 (49.1%) biopsies were positive for HPV16, 10 (18.2%) were positive for HPV but negative for HPV16, and 18 (32.7%) were negative for HPV. A valid result with AP28 was obtained for 51 biopsy samples (92.7%). Among 37 HPV positive samples by IL, 33 (89.2%) were positive by AP28. The agreement between both assays was good (Cohen's kappa = 0.78). Among the six discrepancies between assays, always associated with low HPV16 viral load, four biopsies positive for HPV16 by IL could not be detected by AP28. Taken together, these observations demonstrate that both assays could be used in routine HPV detection and genotyping on FFPE biopsy samples of head and neck tumours.
引用
收藏
页码:421 / 425
页数:5
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