
pmid: 28536155
Abstract The FDA has approved the ALK inhibitor brigatinib for patients with metastatic non-small cell lung cancer who cannot take crizotinib or whose disease worsened despite its use. The decision was based upon results of a phase II study that assessed two drug doses, with overall response rates of 45% and 56% respectively. The drug's effect on overall survival remains unclear, as does the optimal sequence of brigatinib and the three other ALK inhibitors.
Pyridines, United States Food and Drug Administration, Receptor Protein-Tyrosine Kinases, United States, Clinical Trials, Phase II as Topic, Organophosphorus Compounds, Pyrimidines, Crizotinib, Carcinoma, Non-Small-Cell Lung, Humans, Pyrazoles, Anaplastic Lymphoma Kinase, Drug Approval
Pyridines, United States Food and Drug Administration, Receptor Protein-Tyrosine Kinases, United States, Clinical Trials, Phase II as Topic, Organophosphorus Compounds, Pyrimidines, Crizotinib, Carcinoma, Non-Small-Cell Lung, Humans, Pyrazoles, Anaplastic Lymphoma Kinase, Drug Approval
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