Your browser doesn't support javascript.
loading
The prognostic value of PI3K mutational status in breast cancer: A meta-analysis.
Sobhani, Navid; Roviello, Giandomenico; Corona, Silvia P; Scaltriti, Maurizio; Ianza, Anna; Bortul, Marina; Zanconati, Fabrizio; Generali, Daniele.
Afiliação
  • Sobhani N; Department of Medical, Surgical and Health Sciences, Teaching Hospital of Cattinara, University of Trieste, Trieste, Italy.
  • Roviello G; Department of Medical, Surgical and Health Sciences, University of Trieste, Cattinara Academic Hospital, Trieste, Italy.
  • Corona SP; Department of Medical, Surgical and Health Sciences, Teaching Hospital of Cattinara, University of Trieste, Trieste, Italy.
  • Scaltriti M; Department of Oncology, Medical Oncology Unit, San Donato Hospital, Arezzo, Italy.
  • Ianza A; Department of Radiation Oncology, Peter MacCallum Cancer Center, Moorabbin Campus, Bentleigh East, Victoria, Australia.
  • Bortul M; Human Oncology and Pathogenesis Program, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Zanconati F; Department of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
  • Generali D; Department of Medical, Surgical and Health Sciences, Teaching Hospital of Cattinara, University of Trieste, Trieste, Italy.
J Cell Biochem ; 119(6): 4287-4292, 2018 06.
Article em En | MEDLINE | ID: mdl-29345357
ABSTRACT
Breast cancer (BC) is the second most common cause of cancer-related deaths in women worldwide. The availability of reliable biomarkers of response/resistance to cancer treatments would benefit patients and clinicians allowing for a better selection of BC patients most likely to respond to a specific treatment. Phosphatidylinositol 3-kinase (PI3K) enzymes are involved in numerous cellular- functions and processes. The gene encoding for PI3K catalytic subunit p110α is mutated in 20-40% of BC. We performed a meta-analysis of the current literature on randomized clinical trials, investigating the role of PIK3CA mutational status as prognostic factor, and predictor of response to anti-cancer treatments. Overall 1929 cases were included. The pooled analysis confirmed that the presence of a PIK3CA mutation represents an independent negative prognostic factor (HR = 1.67, 95%CI 1.15-2.43; P = 0.007) in BC, as previously reported. As PI3K signaling is also a result of other pathways' hyperactivation, further investigation of potential biomarkers able to predict likelihood of response to anti-PI3K/mTOR, anti-HER2, and other TKRs is warranted in future randomized clinical trials.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Transdução de Sinais / Classe I de Fosfatidilinositol 3-Quinases / Proteínas de Neoplasias Tipo de estudo: Clinical_trials / Diagnostic_studies / Prognostic_studies / Systematic_reviews Limite: Female / Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias da Mama / Transdução de Sinais / Classe I de Fosfatidilinositol 3-Quinases / Proteínas de Neoplasias Tipo de estudo: Clinical_trials / Diagnostic_studies / Prognostic_studies / Systematic_reviews Limite: Female / Humans Idioma: En Ano de publicação: 2018 Tipo de documento: Article