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[Therapeutic impact of molecular diagnosis in metastatic non-small cell lung cancer: targeted therapies in 2013]. / Impact thérapeutique du diagnostic moléculaire des carcinomes bronchiques non à petites cellules métastatiques : les traitements ciblés en 2013.
Pecuchet, N; Bigot, F; Henni, M; Fabre, E.
Afiliação
  • Pecuchet N; Service d'oncologie médicale, hôpital européen Georges-Pompidou, 20-30, rue Leblanc, 75908 Paris cedex 15, France; Unité Inserm U775 : bases moléculaires de la réponse aux xénobiotiques, centre universitaire des Saints-Pères, 45, rue des Saints-Pères, 75006 Paris, France.
  • Bigot F; Service d'oncologie médicale, hôpital européen Georges-Pompidou, 20-30, rue Leblanc, 75908 Paris cedex 15, France.
  • Henni M; Service d'oncologie médicale, hôpital européen Georges-Pompidou, 20-30, rue Leblanc, 75908 Paris cedex 15, France.
  • Fabre E; Service d'oncologie médicale, hôpital européen Georges-Pompidou, 20-30, rue Leblanc, 75908 Paris cedex 15, France; Unité Inserm U775 : bases moléculaires de la réponse aux xénobiotiques, centre universitaire des Saints-Pères, 45, rue des Saints-Pères, 75006 Paris, France. Electronic address: elizabe
Rev Pneumol Clin ; 70(1-2): 38-46, 2014.
Article em Fr | MEDLINE | ID: mdl-24566025
ABSTRACT
Recent advances in the molecular characterization of metastatic unresectable lung cancers have markedly improved the management of patients. Today, molecular tests should be performed routinely in all patients with non-squamous non-small cell lung cancer, and in case of squamous cell carcinoma occurring in a non-smoker. In the presence of EGFR mutation or ALK rearrangement, specific inhibitors have shown superior efficacy to chemotherapy in first-line treatment for anti-EGFR (erlotinib and gefitinib) and in second-line treatment for anti-ALK (crizotinib). We will report the most recent clinical trials that aimed to identify effective therapeutic alternatives in case of acquired resistance to first-generation inhibitors (erlotinib, gefitnib, crizotinib), which inevitably occur in a median of 11-13 months at the first line setting and 7 months at the second line setting. Finally, we will describe more recently known molecular alterations such as ROS1 or RET rearrangements and HER2, BRAF, PIK3CA, DDR2 mutations. Some of these alterations are already elegible for dedicated targeted therapies within clinical trials or temporary use authorization (ATU).
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pirazóis / Piridinas / Quinazolinas / Carcinoma Pulmonar de Células não Pequenas / Técnicas de Diagnóstico Molecular / Inibidores de Proteínas Quinases / Terapia de Alvo Molecular / Neoplasias Pulmonares / Antineoplásicos Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: Fr Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pirazóis / Piridinas / Quinazolinas / Carcinoma Pulmonar de Células não Pequenas / Técnicas de Diagnóstico Molecular / Inibidores de Proteínas Quinases / Terapia de Alvo Molecular / Neoplasias Pulmonares / Antineoplásicos Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Humans Idioma: Fr Ano de publicação: 2014 Tipo de documento: Article