Title : Molecular and clinicopathological characteristics of ROS1-rearranged non-small-cell lung cancers identified by next-generation sequencing.

Pub. Date : 2020 Nov

PMID : 32871626






3 Functional Relationships(s)
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1 The tyrosine kinase inhibitors (TKIs), crizotinib, lorlatinib, and entrectinib have demonstrated favorable efficacy in treating ROS1-rearranged NSCLCs. Crizotinib ROS proto-oncogene 1, receptor tyrosine kinase Homo sapiens
2 ROS1 mutations, including G2032R were observed in approximately 33% of post-crizotinib samples. Crizotinib ROS proto-oncogene 1, receptor tyrosine kinase Homo sapiens
3 Collectively, we report the prevalence of ROS1 fusions in a large-scale NSCLC population, and the efficacy of crizotinib in treating patients with ROS1-rearranged NSCLC. Crizotinib ROS proto-oncogene 1, receptor tyrosine kinase Homo sapiens