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PIK3CA mutations as prognostic factor in squamous cell lung carcinoma.
McGowan, Marc; Hoven, Aleksandra Silye; Lund-Iversen, Marius; Solberg, Steinar; Helland, Åslaug; Hirsch, Fred R; Brustugun, Odd Terje.
Afiliación
  • McGowan M; Dept of Cancer Research, Oslo University Hospital-The Norwegian Radium Hospital, Oslo, Norway.
  • Hoven AS; Dept of Pathology, Oslo University Hospital-The Norwegian Radium Hospital, Oslo, Norway.
  • Lund-Iversen M; Dept of Pathology, Oslo University Hospital-The Norwegian Radium Hospital, Oslo, Norway.
  • Solberg S; Dept of Thoracic Surgery, Oslo University Hospital, Oslo, Norway.
  • Helland Å; Dept of Cancer Research, Oslo University Hospital-The Norwegian Radium Hospital, Oslo, Norway; Dept of Oncology, Oslo University Hospital-The Norwegian Radium Hospital, Oslo, Norway.
  • Hirsch FR; University of Colorado Cancer Center, Denver, CO, USA.
  • Brustugun OT; Dept of Cancer Research, Oslo University Hospital-The Norwegian Radium Hospital, Oslo, Norway; Dept of Oncology, Oslo University Hospital-The Norwegian Radium Hospital, Oslo, Norway. Electronic address: ot.brustugun@gmail.com.
Lung Cancer ; 103: 52-57, 2017 01.
Article en En | MEDLINE | ID: mdl-28024696
ABSTRACT

OBJECTIVES:

Mutation in the PIK3CA gene is reported frequent in squamous cell carcinomas of the lung, but its potential prognostic role is still obscure. We have studied the prognostic importance of PIK3CA mutations as well as the relation to other markers in a large number of early stage lung cancers of squamous carcinoma subtype. PATIENTS AND

METHODS:

Tumour tissue was obtained from 308 consecutively operated lung cancer patients with squamous cell carcinoma in the period 2003-2013. DNA was isolated according to standard procedures, and mutation analysis was done with either the SnapShot method and/or using PIK3CA specific primers in the Cobas system. PD-L1-expression was analysed with immunohistochemistry After thorough follow-up (median 67.6 months), overall survival and time to relapse was calculated.

RESULTS:

Tumour tissue from 102 females and 206 males were analysed. 167 (54.2%) were in stage I, 96 (31.2%) in stage II and 45 (14.6%) in stage III. PIK3CA mutation was found in 35 (11.4%) patients, most frequently in exon 20. There were no differences in sex, stage or smoking behaviour between mutated and non-mutated cases. Patients with PIK3CA mutations had a significantly longer overall survival (p=0.042) and time to relapse (p=0.030) than non-mutated cases, and the difference in time to relapse was also retained in stage I-cases (p=0.044). PD-L1-expression was less frequent among mutated cases.

CONCLUSION:

Our results indicate that PIK3CA mutations may confer a survival advantage in early stage squamous cell lung cancers, but further work is needed to confirm this finding.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Pronóstico / Carcinoma de Células Escamosas / Carcinoma de Pulmón de Células no Pequeñas / Fosfatidilinositol 3-Quinasa Clase I / Neoplasias Pulmonares / Mutación Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Lung Cancer Asunto de la revista: NEOPLASIAS Año: 2017 Tipo del documento: Article País de afiliación: Noruega

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Pronóstico / Carcinoma de Células Escamosas / Carcinoma de Pulmón de Células no Pequeñas / Fosfatidilinositol 3-Quinasa Clase I / Neoplasias Pulmonares / Mutación Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Lung Cancer Asunto de la revista: NEOPLASIAS Año: 2017 Tipo del documento: Article País de afiliación: Noruega