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The utility of TP53 and PIK3CA mutations as prognostic biomarkers in salivary adenoid cystic carcinoma.
Adderley, Helen; Rack, Samuel; Hapuarachi, Brindley; Feeney, Laura; Morgan, David; Hussell, Tracy; Wallace, Andrew J; Betts, Guy; Hodgson, Clare; Harrington, Kevin; Metcalf, Robert.
Afiliación
  • Adderley H; The Christie NHS Foundation Trust, Manchester, United Kingdom.
  • Rack S; Manchester University NHS Foundation Trust, Manchester, United Kingdom.
  • Hapuarachi B; The Christie NHS Foundation Trust, Manchester, United Kingdom.
  • Feeney L; Queen's University Belfast, Belfast, United Kingdom.
  • Morgan D; The University of Manchester, Manchester, United Kingdom.
  • Hussell T; The University of Manchester, Manchester, United Kingdom.
  • Wallace AJ; NW GLH, Manchester University NHS Foundation Trust, Manchester, United Kingdom.
  • Betts G; Manchester University NHS Foundation Trust, Manchester, United Kingdom.
  • Hodgson C; The Christie NHS Foundation Trust, Manchester, United Kingdom.
  • Harrington K; The Institute of Cancer Research and The Royal Marsden NHS Foundation Trust National Institute of Health Research Biomedical Research Centre, London, United Kingdom.
  • Metcalf R; The Christie NHS Foundation Trust, Manchester, United Kingdom. Electronic address: robert.metcalf1@nhs.net.
Oral Oncol ; 113: 105095, 2021 02.
Article en En | MEDLINE | ID: mdl-33290961
ABSTRACT

OBJECTIVES:

Despite wide excision and post-operative irradiation, loco-regional and/or metastatic recurrence is a significant clinical problem in salivary adenoid cystic carcinoma (SACC). Reliable biomarkers are required to tailor post-treatment surveillance to patients at highest risk of recurrence. We sought to determine the utility of TP53 and PIK3CA mutations as prognostic biomarkers in SACC. MATERIALS AND

METHODS:

DNA was extracted from archival tumour blocks of 145 SACC patients from 66 UK referral centres and sequenced for TP53 and PIK3CA mutations. Clinical, pathological and outcome data were analysed to determine the impact of the genomic alterations on disease recurrence and overall survival (OS).

RESULTS:

TP53 and PIK3CA mutations were identified in 8% (10/121 successful analyses) and 2% (3/121) of cases, respectively. There were too few PIK3CA mutations in this cohort for informative further analysis. TP53-mutated SACC had significantly shorter median OS (5.3 vs. 16.3 years, p = 0.019) and lower 10-year survival (48% vs. 81%) compared with TP53 wild-type ACC. Solid-pattern histopathology was more frequent in TP53-mutated SACC (50% vs. 15%, p = 0.27).

CONCLUSION:

TP53-mutated recurrent and metastatic SACC was associated with shorter OS, which was significant when combined with published genomic data sets. Stratifying by TP53 status, in addition to established clinical, pathological and genomic biomarkers, may usefully inform follow-up strategy.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias de las Glándulas Salivales / Biomarcadores de Tumor / Proteína p53 Supresora de Tumor / Carcinoma Adenoide Quístico / Fosfatidilinositol 3-Quinasa Clase I Tipo de estudio: Prognostic_studies Límite: Female / Humans / Male Idioma: En Revista: Oral Oncol Asunto de la revista: NEOPLASIAS Año: 2021 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias de las Glándulas Salivales / Biomarcadores de Tumor / Proteína p53 Supresora de Tumor / Carcinoma Adenoide Quístico / Fosfatidilinositol 3-Quinasa Clase I Tipo de estudio: Prognostic_studies Límite: Female / Humans / Male Idioma: En Revista: Oral Oncol Asunto de la revista: NEOPLASIAS Año: 2021 Tipo del documento: Article País de afiliación: Reino Unido