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[New therapeutical strategies in metastatic hormone-dependent breast cancer]. / Nouvelles stratégies thérapeutiques dans le cancer du sein hormono-dépendant métastatique.
Vilquin, Paul; Cohen, Pascale; Maudelonde, Thierry; Tredan, Olivier; Treilleux, Isabelle; Bachelot, Thomas; Heudel, Pierre-Etienne.
Afiliación
  • Vilquin P; CHU de Montpellier, laboratoire de biologie cellulaire, 34295 Montpellier, France. Electronic address: p-vilquin@chu-montpellier.fr.
  • Cohen P; Université Lyon 1, faculté de pharmacie, institut des sciences pharmaceutiques et biologiques (ISPB), 69008 Lyon, France; Centre de recherche en cancérologie de Lyon, Inserm U1052, CNRS UMR 5286, 69008 Lyon, France.
  • Maudelonde T; CHU de Montpellier, laboratoire de biologie cellulaire, 34295 Montpellier, France.
  • Tredan O; Centre Léon-Bérard, 69008 Lyon, France.
  • Treilleux I; Centre de recherche en cancérologie de Lyon, Inserm U1052, CNRS UMR 5286, 69008 Lyon, France; Centre Léon-Bérard, 69008 Lyon, France.
  • Bachelot T; Centre Léon-Bérard, 69008 Lyon, France.
  • Heudel PE; Centre Léon-Bérard, 69008 Lyon, France.
Bull Cancer ; 102(4): 367-80, 2015 Apr.
Article en Fr | MEDLINE | ID: mdl-25799877
Hormone-dependent breast cancer is the first example of cancer treated by targeted therapy for more than 30 years. Blocking estrogen pathway was the first therapeutical strategy for this subtype of breast cancer, and remains the principle of current standard treatment. Despite the efficacy of drugs used in endocrine therapy, hormone resistance is a major problem for the management of patients with hormone-dependent breast cancer. In this review, we will discuss the development of strategies targeting the PI3K/Akt/mTOR pathway, CDK4/6 (Cyclin Dependent Kinase 4/6) and FGFR (Fibroblast Growth Factor Receptor) in hormone-dependent metastatic breast cancer (ER+). Recent results of clinical trials showed that combination of endocrine therapy with such pharmacological inhibitors is a promising strategy to overcome endocrine resistance. Mutated forms and isoforms of ERα have been recently discovered and its targeting could represent an therapeutic alternative. Future progress will focus on the identification of new compounds and combinations with other targeted therapies to improve the efficacy of such inhibitors in clinical practice.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias de la Mama / Resistencia a Antineoplásicos / Antineoplásicos Hormonales / Neoplasias Hormono-Dependientes Tipo de estudio: Prognostic_studies Límite: Female / Humans Idioma: Fr Revista: Bull Cancer Año: 2015 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Neoplasias de la Mama / Resistencia a Antineoplásicos / Antineoplásicos Hormonales / Neoplasias Hormono-Dependientes Tipo de estudio: Prognostic_studies Límite: Female / Humans Idioma: Fr Revista: Bull Cancer Año: 2015 Tipo del documento: Article
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