Please use this identifier to cite or link to this item:
https://doi.org/10.1186/s12943-018-0778-0
DC Field | Value | |
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dc.title | Third generation EGFR TKIs: Current data and future directions | |
dc.contributor.author | Tan, C.-S | |
dc.contributor.author | Kumarakulasinghe, N.B | |
dc.contributor.author | Huang, Y.-Q | |
dc.contributor.author | Ang, Y.L.E | |
dc.contributor.author | Choo, J.R.-E | |
dc.contributor.author | Goh, B.-C | |
dc.contributor.author | Soo, R.A | |
dc.date.accessioned | 2020-10-27T10:14:05Z | |
dc.date.available | 2020-10-27T10:14:05Z | |
dc.date.issued | 2018 | |
dc.identifier.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 | |
dc.identifier.issn | 14764598 | |
dc.identifier.uri | https://scholarbank.nus.edu.sg/handle/10635/181215 | |
dc.description.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). | |
dc.rights | Attribution 4.0 International | |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | |
dc.source | Unpaywall 20201031 | |
dc.subject | avitinib | |
dc.subject | brigatinib | |
dc.subject | circulating tumor DNA | |
dc.subject | epidermal growth factor receptor | |
dc.subject | epidermal growth factor receptor kinase inhibitor | |
dc.subject | erlotinib | |
dc.subject | fibroblast growth factor receptor 1 | |
dc.subject | gefitinib | |
dc.subject | K ras protein | |
dc.subject | mavelertinib | |
dc.subject | mitogen activated protein kinase | |
dc.subject | naquotinib | |
dc.subject | nazartinib | |
dc.subject | olmutinib | |
dc.subject | osimertinib | |
dc.subject | pemetrexed | |
dc.subject | phosphatidylinositol 3 kinase | |
dc.subject | platinum derivative | |
dc.subject | rociletinib | |
dc.subject | unclassified drug | |
dc.subject | yh 25448 | |
dc.subject | osimertinib | |
dc.subject | piperazine derivative | |
dc.subject | protein kinase inhibitor | |
dc.subject | acne | |
dc.subject | anemia | |
dc.subject | C797S gene | |
dc.subject | cancer growth | |
dc.subject | cell transformation | |
dc.subject | central nervous system metastasis | |
dc.subject | circulating tumor cell | |
dc.subject | decreased appetite | |
dc.subject | diarrhea | |
dc.subject | disease control | |
dc.subject | drug development | |
dc.subject | drug dose escalation | |
dc.subject | drug dose increase | |
dc.subject | drug efficacy | |
dc.subject | drug indication | |
dc.subject | drug resistance | |
dc.subject | drug response | |
dc.subject | drug safety | |
dc.subject | drug selectivity | |
dc.subject | drug tolerance | |
dc.subject | drug withdrawal | |
dc.subject | dry skin | |
dc.subject | exon | |
dc.subject | fatigue | |
dc.subject | FGFR1 gene | |
dc.subject | gene | |
dc.subject | gene amplification | |
dc.subject | gene mutation | |
dc.subject | hepatitis B | |
dc.subject | human | |
dc.subject | hypertransaminasemia | |
dc.subject | incidence | |
dc.subject | interstitial lung disease | |
dc.subject | maculopapular rash | |
dc.subject | MAPK gene | |
dc.subject | nausea | |
dc.subject | non small cell lung cancer | |
dc.subject | oncogene K ras | |
dc.subject | paronychia | |
dc.subject | patient-reported outcome | |
dc.subject | PIK3CA gene | |
dc.subject | pneumonia | |
dc.subject | progression free survival | |
dc.subject | pruritus | |
dc.subject | QT prolongation | |
dc.subject | rash | |
dc.subject | Review | |
dc.subject | rhinorrhea | |
dc.subject | stomatitis | |
dc.subject | T790 M gene | |
dc.subject | tumor biopsy | |
dc.subject | animal | |
dc.subject | antagonists and inhibitors | |
dc.subject | genetics | |
dc.subject | metabolism | |
dc.subject | mutation | |
dc.subject | Animals | |
dc.subject | Carcinoma, Non-Small-Cell Lung | |
dc.subject | ErbB Receptors | |
dc.subject | Humans | |
dc.subject | Mutation | |
dc.subject | Piperazines | |
dc.subject | Protein Kinase Inhibitors | |
dc.type | Review | |
dc.contributor.department | PHARMACOLOGY | |
dc.contributor.department | CANCER SCIENCE INSTITUTE OF SINGAPORE | |
dc.description.doi | 10.1186/s12943-018-0778-0 | |
dc.description.sourcetitle | Molecular Cancer | |
dc.description.volume | 17 | |
dc.description.issue | 1 | |
dc.description.page | 29 | |
Appears in Collections: | Staff Publications Elements |
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