Your browser doesn't support javascript.
loading
Prognostic Analysis of HPV Status in Sinonasal Squamous Cell Carcinoma.
Tendron, Alexandre; Classe, Marion; Casiraghi, Odile; Pere, Hélène; Even, Caroline; Gorphe, Philippe; Moya-Plana, Antoine.
Afiliação
  • Tendron A; Head and Neck Oncology Department, Gustave Roussy Cancer Campus, Université Paris Saclay, 94805 Villejuif, France.
  • Classe M; Molecular Radiotherapy and Therapeutic Innovation, UMR 1030, 94805 Villejuif, France.
  • Casiraghi O; Molecular Radiotherapy and Therapeutic Innovation, UMR 1030, 94805 Villejuif, France.
  • Pere H; Pathology Department, Gustave Roussy Cancer Campus, Université Paris Saclay, 94805 Villejuif, France.
  • Even C; Pathology Department, Gustave Roussy Cancer Campus, Université Paris Saclay, 94805 Villejuif, France.
  • Gorphe P; Virology Department, European Hospital Georges Pompidou, 75015 Paris, France.
  • Moya-Plana A; Functional Genomics of Solid Tumors (FunGeST), INSERM, Centre de Recherche des Cordeliers, Paris and Sorbonne Université, 75006 Paris, France.
Cancers (Basel) ; 14(8)2022 Apr 08.
Article em En | MEDLINE | ID: mdl-35454782
Sinonasal squamous cell carcinoma (SNSCC) is a rare and aggressive malignancy with poor prognosis. Human papilloma virus (HPV) can induce SNSCC although its incidence and impact on patients' outcomes remains unclear. We performed a retrospective cohort study of patients with SNSCC treated consecutively in a comprehensive cancer center. HPV status was determined with p16 immunohistochemistry followed by RNA in situ hybridization (RNAscope). The incidence, clinical characteristics, and oncologic outcomes of HPV+SNSCC were assessed. P16 prognostic value was evaluated. Fifty-nine patients were included. Eleven (18.6%) SNSCC were p16+ with five (8.4%) doubtful cases. RNAscope was positive in nine cases (15.2%). Patients with HPV+SNSCC were younger (p = 0.0298) with a primary tumor originating mainly in nasal fossa (p < 10−4). Pathologic findings were not different according to HPV status. Among patients who were curatively treated, overall survival was better for HPV+SNSCC (p = 0.022). No prognostic value of p16 expression was reported. Patients with HPV+SNSCC have better oncologic outcomes, probably due to earlier tumor stage with primary location predominantly in the nasal fossa, a more suitable epicenter to perform a surgical resection with clear margins. P16 expression seems not to be a good surrogate of HPV status in SNSCC.
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Cancers (Basel) Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Cancers (Basel) Ano de publicação: 2022 Tipo de documento: Article