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[Cabozantinib: Mechanism of action, efficacy and indications]. / Cabozantinib : modalités d'action, efficacité et indications.
Cochin, Valérie; Gross-Goupil, Marine; Ravaud, Alain; Godbert, Yann; Le Moulec, Sylvestre.
Afiliação
  • Cochin V; Centre hospitalo-universitaire de Bordeaux, hôpital Saint-André, 01, rue Jean-Burguet, 33075 Bordeaux cedex, France. Electronic address: valerie.cochin@chu-bordeaux.fr.
  • Gross-Goupil M; Centre hospitalo-universitaire de Bordeaux, hôpital Saint-André, 01, rue Jean-Burguet, 33075 Bordeaux cedex, France.
  • Ravaud A; Centre hospitalo-universitaire de Bordeaux, hôpital Saint-André, 01, rue Jean-Burguet, 33075 Bordeaux cedex, France; Université de Bordeaux, 146, rue Léo-Saignat, 33076 Bordeaux cedex, France.
  • Godbert Y; Institut Bergonié, centre de lutte contre le cancer de Bordeaux, 229, cours de l'Argonne, 33076 Bordeaux cedex, France.
  • Le Moulec S; Institut Bergonié, centre de lutte contre le cancer de Bordeaux, 229, cours de l'Argonne, 33076 Bordeaux cedex, France.
Bull Cancer ; 104(5): 393-401, 2017 May.
Article em Fr | MEDLINE | ID: mdl-28477875
Cabozantinib is an oral multiple tyrosine kinase receptor inhibitor (ITK): VEGFR2, c-MET and RET. Inhibition of VEGFR and c-MET decrease resistance of VEGFR inhibitor via c-MET axis. Cabozantinib improve progression-free survival (PFS) in progressive metastatic medullary thyroid cancer (MTC): 4 months in the placebo group and 11.2 months in the cabozantinib group (P<0.001) in all patient subgroups including those with or without prior ITK and RET mutation status. Cabozantinib increased overall survival (OS) compared with everolimus in patients with advanced renal cell carcinoma who progressed after previous VEGFR ITK treatment: 21.4 months in cabozantinib group and 16.5 months in everolimus group (P<0.0003). Cabozantinib obtained the AMM for the treatment of progressive metastatic MTC and advanced renal cell carcinoma. Cabozantinib is a new option in the treatment of MTC by inclusion in therapeutic trials (no payment in this indication) and advanced renal cell carcinoma (hospital delivery). Its tolerance is similar to anti-angiogenic therapies and justifies an optimal management of the secondary effect.
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Piridinas / Receptores Proteína Tirosina Quinases / Anilidas / Antineoplásicos Tipo de estudo: Clinical_trials Limite: Humans / Male Idioma: Fr Revista: Bull Cancer Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Piridinas / Receptores Proteína Tirosina Quinases / Anilidas / Antineoplásicos Tipo de estudo: Clinical_trials Limite: Humans / Male Idioma: Fr Revista: Bull Cancer Ano de publicação: 2017 Tipo de documento: Article