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https://doi.org/10.1186/s12943-018-0778-0
Title: | Third generation EGFR TKIs: Current data and future directions | Authors: | Tan, C.-S Kumarakulasinghe, N.B Huang, Y.-Q Ang, Y.L.E Choo, J.R.-E Goh, B.-C Soo, R.A |
Keywords: | avitinib brigatinib circulating tumor DNA epidermal growth factor receptor epidermal growth factor receptor kinase inhibitor erlotinib fibroblast growth factor receptor 1 gefitinib K ras protein mavelertinib mitogen activated protein kinase naquotinib nazartinib olmutinib osimertinib pemetrexed phosphatidylinositol 3 kinase platinum derivative rociletinib unclassified drug yh 25448 osimertinib piperazine derivative protein kinase inhibitor acne anemia C797S gene cancer growth cell transformation central nervous system metastasis circulating tumor cell decreased appetite diarrhea disease control drug development drug dose escalation drug dose increase drug efficacy drug indication drug resistance drug response drug safety drug selectivity drug tolerance drug withdrawal dry skin exon fatigue FGFR1 gene gene gene amplification gene mutation hepatitis B human hypertransaminasemia incidence interstitial lung disease maculopapular rash MAPK gene nausea non small cell lung cancer oncogene K ras paronychia patient-reported outcome PIK3CA gene pneumonia progression free survival pruritus QT prolongation rash Review rhinorrhea stomatitis T790 M gene tumor biopsy animal antagonists and inhibitors genetics metabolism mutation Animals Carcinoma, Non-Small-Cell Lung ErbB Receptors Humans Mutation Piperazines Protein Kinase Inhibitors |
Issue Date: | 2018 | Citation: | Tan, C.-S, Kumarakulasinghe, N.B, Huang, Y.-Q, Ang, Y.L.E, Choo, J.R.-E, Goh, B.-C, Soo, R.A (2018). Third generation EGFR TKIs: Current data and future directions. Molecular Cancer 17 (1) : 29. ScholarBank@NUS Repository. https://doi.org/10.1186/s12943-018-0778-0 | Rights: | Attribution 4.0 International | Abstract: | Acquired T790 M mutation is the commonest cause of resistance for advanced non-small cell lung cancer (NSCLC) epidermal growth factor receptor (EGFR) mutant patients who had progressed after first line EGFR TKI (tyrosine kinase inhibitor). Several third generation EGFR TKIs which are EGFR mutant selective and wild-type (WT) sparing were developed to treat these patients with T790 M acquired resistant mutation. Osimertinib is one of the third generation EGFR TKIs and is currently the most advanced in clinical development. Unfortunately, despite good initial response, patients who was treated with third generation EGFR TKI would develop acquired resistance and several mechanisms had been identified and the commonest being C797S mutation at exon 20. Several novel treatment options were being developed for patients who had progressed on third generation EGFR TKI but they are still in the early phase of development. Osimertinib under FLAURA study had been shown to have better progression-free survival over first generation EGFR TKI in the first line setting and likely will become the new standard of care. © 2018 The Author(s). | Source Title: | Molecular Cancer | URI: | https://scholarbank.nus.edu.sg/handle/10635/181215 | ISSN: | 14764598 | DOI: | 10.1186/s12943-018-0778-0 | Rights: | Attribution 4.0 International |
Appears in Collections: | Staff Publications Elements |
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