Please use this identifier to cite or link to this item: https://doi.org/10.1186/s12943-018-0778-0
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dc.titleThird generation EGFR TKIs: Current data and future directions
dc.contributor.authorTan, C.-S
dc.contributor.authorKumarakulasinghe, N.B
dc.contributor.authorHuang, Y.-Q
dc.contributor.authorAng, Y.L.E
dc.contributor.authorChoo, J.R.-E
dc.contributor.authorGoh, B.-C
dc.contributor.authorSoo, R.A
dc.date.accessioned2020-10-27T10:14:05Z
dc.date.available2020-10-27T10:14:05Z
dc.date.issued2018
dc.identifier.citationTan, 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
dc.identifier.issn14764598
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/181215
dc.description.abstractAcquired 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).
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectavitinib
dc.subjectbrigatinib
dc.subjectcirculating tumor DNA
dc.subjectepidermal growth factor receptor
dc.subjectepidermal growth factor receptor kinase inhibitor
dc.subjecterlotinib
dc.subjectfibroblast growth factor receptor 1
dc.subjectgefitinib
dc.subjectK ras protein
dc.subjectmavelertinib
dc.subjectmitogen activated protein kinase
dc.subjectnaquotinib
dc.subjectnazartinib
dc.subjectolmutinib
dc.subjectosimertinib
dc.subjectpemetrexed
dc.subjectphosphatidylinositol 3 kinase
dc.subjectplatinum derivative
dc.subjectrociletinib
dc.subjectunclassified drug
dc.subjectyh 25448
dc.subjectosimertinib
dc.subjectpiperazine derivative
dc.subjectprotein kinase inhibitor
dc.subjectacne
dc.subjectanemia
dc.subjectC797S gene
dc.subjectcancer growth
dc.subjectcell transformation
dc.subjectcentral nervous system metastasis
dc.subjectcirculating tumor cell
dc.subjectdecreased appetite
dc.subjectdiarrhea
dc.subjectdisease control
dc.subjectdrug development
dc.subjectdrug dose escalation
dc.subjectdrug dose increase
dc.subjectdrug efficacy
dc.subjectdrug indication
dc.subjectdrug resistance
dc.subjectdrug response
dc.subjectdrug safety
dc.subjectdrug selectivity
dc.subjectdrug tolerance
dc.subjectdrug withdrawal
dc.subjectdry skin
dc.subjectexon
dc.subjectfatigue
dc.subjectFGFR1 gene
dc.subjectgene
dc.subjectgene amplification
dc.subjectgene mutation
dc.subjecthepatitis B
dc.subjecthuman
dc.subjecthypertransaminasemia
dc.subjectincidence
dc.subjectinterstitial lung disease
dc.subjectmaculopapular rash
dc.subjectMAPK gene
dc.subjectnausea
dc.subjectnon small cell lung cancer
dc.subjectoncogene K ras
dc.subjectparonychia
dc.subjectpatient-reported outcome
dc.subjectPIK3CA gene
dc.subjectpneumonia
dc.subjectprogression free survival
dc.subjectpruritus
dc.subjectQT prolongation
dc.subjectrash
dc.subjectReview
dc.subjectrhinorrhea
dc.subjectstomatitis
dc.subjectT790 M gene
dc.subjecttumor biopsy
dc.subjectanimal
dc.subjectantagonists and inhibitors
dc.subjectgenetics
dc.subjectmetabolism
dc.subjectmutation
dc.subjectAnimals
dc.subjectCarcinoma, Non-Small-Cell Lung
dc.subjectErbB Receptors
dc.subjectHumans
dc.subjectMutation
dc.subjectPiperazines
dc.subjectProtein Kinase Inhibitors
dc.typeReview
dc.contributor.departmentPHARMACOLOGY
dc.contributor.departmentCANCER SCIENCE INSTITUTE OF SINGAPORE
dc.description.doi10.1186/s12943-018-0778-0
dc.description.sourcetitleMolecular Cancer
dc.description.volume17
dc.description.issue1
dc.description.page29
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