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Precision Medicine to Treat Advanced Gastroesophageal Adenocarcinoma: A Work in Progress.
Gambardella, Valentina; Fleitas, Tania; Tarazona, Noelia; Papaccio, Federica; Huerta, Marisol; Roselló, Susana; Gimeno-Valiente, Francisco; Roda, Desamparados; Cervantes, Andrés.
Afiliación
  • Gambardella V; Department of Medical Oncology, Biomedical Research Institute INCLIVA, University of Valencia, Blasco Ibañez 17, 46010 Valencia, Spain.
  • Fleitas T; Instituto de Salud Carlos III, CIBERONC, 28000 Madrid, Spain.
  • Tarazona N; Department of Medical Oncology, Biomedical Research Institute INCLIVA, University of Valencia, Blasco Ibañez 17, 46010 Valencia, Spain.
  • Papaccio F; Instituto de Salud Carlos III, CIBERONC, 28000 Madrid, Spain.
  • Huerta M; Department of Medical Oncology, Biomedical Research Institute INCLIVA, University of Valencia, Blasco Ibañez 17, 46010 Valencia, Spain.
  • Roselló S; Instituto de Salud Carlos III, CIBERONC, 28000 Madrid, Spain.
  • Gimeno-Valiente F; Department of Medical Oncology, Biomedical Research Institute INCLIVA, University of Valencia, Blasco Ibañez 17, 46010 Valencia, Spain.
  • Roda D; Department of Medical Oncology, Biomedical Research Institute INCLIVA, University of Valencia, Blasco Ibañez 17, 46010 Valencia, Spain.
  • Cervantes A; Department of Medical Oncology, Biomedical Research Institute INCLIVA, University of Valencia, Blasco Ibañez 17, 46010 Valencia, Spain.
J Clin Med ; 9(9)2020 Sep 22.
Article en En | MEDLINE | ID: mdl-32971757
ABSTRACT
Gastroesophageal adenocarcinoma (GEA) represents a heterogeneous disease and, when diagnosed as locally advanced or metastatic, it is characterized by poor prognosis. During the last few years, several molecular classifications have been proposed to try to personalize treatment for those patients diagnosed with advanced disease. Nevertheless, despite the great effort, precision medicine is still far from being a reality. The improvement in the molecular analysis due to the application of high throughput technologies based on DNA and RNA sequencing has opened a novel scenario leading to the personalization of treatment. The possibility to target epidermal growth factor receptor (HER)2, Claudine, Fibroblast Growth Factor Receptors (FGFR), and other alterations with a molecular matched therapy could significantly improve clinical outcomes over advanced gastric cancer patients. On the other hand, the development of immunotherapy could also represent a promising strategy in a selected population. In this review, we sought to describe the novel pathways implicated in GEA progression and the results of the molecular matched therapies.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: J Clin Med Año: 2020 Tipo del documento: Article País de afiliación: España

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: J Clin Med Año: 2020 Tipo del documento: Article País de afiliación: España