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Classification of Vulvar Squamous Cell Carcinoma and Precursor Lesions by p16 and p53 Immunohistochemistry: Considerations, Caveats, and an Algorithmic Approach.
Yang, Hang; Almadani, Noorah; Thompson, Emily F; Tessier-Cloutier, Basile; Chen, Julia; Ho, Julie; Senz, Janine; McConechy, Melissa K; Chow, Christine; Ta, Monica; Cheng, Angela; Karnezis, Anthony; Huvila, Jutta; McAlpine, Jessica N; Gilks, Blake; Jamieson, Amy; Hoang, Lynn N.
Afiliação
  • Yang H; Pathology and Laboratory Medicine, University of British Columbia and Vancouver General Hospital, British Columbia, Canada.
  • Almadani N; Department of Pathology, Ministry of the National Guard - Health Affairs, and King Abdullah International Medical Research Center, Riyadh, Saudi Arabia.
  • Thompson EF; Pathology and Laboratory Medicine, University of British Columbia and Vancouver General Hospital, British Columbia, Canada.
  • Tessier-Cloutier B; Pathology and Laboratory Medicine, McGill University Health Centre, Quebec, Canada.
  • Chen J; Medical Undergraduate Program, University of British Columbia, British Columbia, Canada.
  • Ho J; Pathology and Laboratory Medicine, University of British Columbia and Vancouver General Hospital, British Columbia, Canada; Genetic Pathology Evaluation Center (GPEC) and Molecular and Advanced Pathology Core (MAPcore), British Columbia, Canada.
  • Senz J; Molecular Oncology, British Columbia Cancer Research Centre, Vancouver, British Columbia, Canada.
  • McConechy MK; Imagia Canexia Health, Vancouver, British Columbia, Canada.
  • Chow C; Genetic Pathology Evaluation Center (GPEC) and Molecular and Advanced Pathology Core (MAPcore), British Columbia, Canada.
  • Ta M; Genetic Pathology Evaluation Center (GPEC) and Molecular and Advanced Pathology Core (MAPcore), British Columbia, Canada.
  • Cheng A; Genetic Pathology Evaluation Center (GPEC) and Molecular and Advanced Pathology Core (MAPcore), British Columbia, Canada.
  • Karnezis A; Pathology and Laboratory Medicine, UC Davis Medical Center, California.
  • Huvila J; Department of Pathology, University of Turku, Turku University Hospital, Turku, Finland.
  • McAlpine JN; Gynecologic Oncology, University of British Columbia, Vancouver, British Columbia, Canada.
  • Gilks B; Pathology and Laboratory Medicine, University of British Columbia and Vancouver General Hospital, British Columbia, Canada; Genetic Pathology Evaluation Center (GPEC) and Molecular and Advanced Pathology Core (MAPcore), British Columbia, Canada.
  • Jamieson A; Gynecologic Oncology, University of British Columbia, Vancouver, British Columbia, Canada.
  • Hoang LN; Pathology and Laboratory Medicine, University of British Columbia and Vancouver General Hospital, British Columbia, Canada; Genetic Pathology Evaluation Center (GPEC) and Molecular and Advanced Pathology Core (MAPcore), British Columbia, Canada. Electronic address: Lien.Hoang@vch.ca.
Mod Pathol ; 36(6): 100145, 2023 06.
Article em En | MEDLINE | ID: mdl-36828360
ABSTRACT
There is emerging evidence that vulvar squamous cell carcinoma (VSCC) can be prognostically subclassified into 3 groups based on human papillomavirus (HPV) and p53 status HPV-associated (HPV+), HPV-independent/p53 wild-type (HPV-/p53wt), or HPV-independent/p53 abnormal (HPV-/p53abn). Our goal was to assess the feasibility of separating VSCC and its precursors into these 3 groups using p16 and p53 immunohistochemistry (IHC). A tissue microarray containing 225 VSCC, 43 usual vulvar intraepithelial neoplasia (uVIN/HSIL), 10 verruciform acanthotic vulvar intraepithelial neoplasia (vaVIN), and 34 differentiated VIN (dVIN), was stained for p16 and p53. Noncomplementary p16 and p53 patterns were resolved by repeating p53 IHC and HPV RNA in situ hybridization (ISH) on whole sections, and sequencing for TP53. Of 82 p16-positive VSCC, 73 (89%) had complementary p16 and p53 patterns and were classified into the HPV+ group, 4 (4.9%) had wild-type p53 staining, positive HPV ISH and were classified into the HPV+ group, whereas 5 (6.1%) had p53 abnormal IHC patterns (1 null, 4 overexpression), negativity for HPV ISH, and harbored TP53 mutations (1 splice site, 4 missense); they were classified as HPV-/p53abn. Of 143 p16-negative VSCC, 142 (99.3%) had complementary p53 and p16 patterns 115 (80.4%) HPV-/p53abn and 27 (18.9%) HPV-/p53wt. One had a basal-sparing p53 pattern, positivity for HPV ISH and was negative for TP53 mutations-HPV+ category. The use of IHC also led to revised diagnoses-HSIL to dVIN (3/43), dVIN to vaVIN (8/34), and dVIN to HSIL (3/34). Overall, 215/225 VSCC (95.6%) could be easily classifiable into 3 groups with p16 and p53 IHC. We identified several caveats, with the major caveat being that "double-positive" p16/p53 should be classified as HPV-/p53abn. We propose an algorithm that will facilitate the application of p16 and p53 IHC to classify VSCC in pathology practice.
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Texto completo: 1 Coleções: 01-internacional Temas: Geral / Tipos_de_cancer / Outros_tipos Base de dados: MEDLINE Assunto principal: Neoplasias Vulvares / Carcinoma in Situ / Carcinoma de Células Escamosas / Infecções por Papillomavirus / Lesões Intraepiteliais Escamosas Limite: Female / Humans Idioma: En Revista: Mod Pathol Assunto da revista: PATOLOGIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Coleções: 01-internacional Temas: Geral / Tipos_de_cancer / Outros_tipos Base de dados: MEDLINE Assunto principal: Neoplasias Vulvares / Carcinoma in Situ / Carcinoma de Células Escamosas / Infecções por Papillomavirus / Lesões Intraepiteliais Escamosas Limite: Female / Humans Idioma: En Revista: Mod Pathol Assunto da revista: PATOLOGIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Canadá