Difference between revisions of "Epidermal growth factor receptor inhibitors"
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First generation: | First generation: | ||
*[[Gefitinib]] (Iressa).<ref name=pmid20855837/> | *[[Gefitinib]] (Iressa).<ref name=pmid20855837/> | ||
*[[Erlotinib]] (Tarceva).<ref name=pmid20855837>{{cite journal |author=Sun Y, Ren Y, Fang Z, ''et al.'' |title=Lung adenocarcinoma from East Asian never-smokers is a disease largely defined by targetable oncogenic mutant kinases |journal=J. Clin. Oncol. |volume=28 |issue=30 |pages=4616–20 |year=2010 |month=October |pmid=20855837 |doi=10.1200/JCO.2010.29.6038 |url=}}</ref> | *[[Erlotinib]] (''Tarceva'' Roche).<ref name=pmid20855837>{{cite journal |author=Sun Y, Ren Y, Fang Z, ''et al.'' |title=Lung adenocarcinoma from East Asian never-smokers is a disease largely defined by targetable oncogenic mutant kinases |journal=J. Clin. Oncol. |volume=28 |issue=30 |pages=4616–20 |year=2010 |month=October |pmid=20855837 |doi=10.1200/JCO.2010.29.6038 |url=}}</ref> | ||
*Afatinib (Gilotrif) - esp. effective when del19 is present.<ref>{{Cite journal | last1 = Yang | first1 = JC. | last2 = Wu | first2 = YL. | last3 = Schuler | first3 = M. | last4 = Sebastian | first4 = M. | last5 = Popat | first5 = S. | last6 = Yamamoto | first6 = N. | last7 = Zhou | first7 = C. | last8 = Hu | first8 = CP. | last9 = O'Byrne | first9 = K. | title = Afatinib versus cisplatin-based chemotherapy for EGFR mutation-positive lung adenocarcinoma (LUX-Lung 3 and LUX-Lung 6): analysis of overall survival data from two randomised, phase 3 trials. | journal = Lancet Oncol | volume = 16 | issue = 2 | pages = 141-51 | month = Feb | year = 2015 | doi = 10.1016/S1470-2045(14)71173-8 | PMID = 25589191 }}</ref> | *Afatinib (Gilotrif) - esp. effective when del19 is present.<ref>{{Cite journal | last1 = Yang | first1 = JC. | last2 = Wu | first2 = YL. | last3 = Schuler | first3 = M. | last4 = Sebastian | first4 = M. | last5 = Popat | first5 = S. | last6 = Yamamoto | first6 = N. | last7 = Zhou | first7 = C. | last8 = Hu | first8 = CP. | last9 = O'Byrne | first9 = K. | title = Afatinib versus cisplatin-based chemotherapy for EGFR mutation-positive lung adenocarcinoma (LUX-Lung 3 and LUX-Lung 6): analysis of overall survival data from two randomised, phase 3 trials. | journal = Lancet Oncol | volume = 16 | issue = 2 | pages = 141-51 | month = Feb | year = 2015 | doi = 10.1016/S1470-2045(14)71173-8 | PMID = 25589191 }}</ref> | ||
Second generation: | Second generation: | ||
Revision as of 19:34, 8 November 2018
Epidermal growth factor receptor inhibitors, abbreviated EGFR inhibitors, is a class of drugs that blocks the EGF receptor.
Drugs
First generation:
- Gefitinib (Iressa).[1]
- Erlotinib (Tarceva Roche).[1]
- Afatinib (Gilotrif) - esp. effective when del19 is present.[2]
Second generation:
Note:
- Both gefitinib and erlotinib are also classified as tyrosine kinase inhibitors (TKIs).
Use
References
- ↑ 1.0 1.1 Sun Y, Ren Y, Fang Z, et al. (October 2010). "Lung adenocarcinoma from East Asian never-smokers is a disease largely defined by targetable oncogenic mutant kinases". J. Clin. Oncol. 28 (30): 4616–20. doi:10.1200/JCO.2010.29.6038. PMID 20855837.
- ↑ Yang, JC.; Wu, YL.; Schuler, M.; Sebastian, M.; Popat, S.; Yamamoto, N.; Zhou, C.; Hu, CP. et al. (Feb 2015). "Afatinib versus cisplatin-based chemotherapy for EGFR mutation-positive lung adenocarcinoma (LUX-Lung 3 and LUX-Lung 6): analysis of overall survival data from two randomised, phase 3 trials.". Lancet Oncol 16 (2): 141-51. doi:10.1016/S1470-2045(14)71173-8. PMID 25589191.
- ↑ Mok, TS.; Cheng, Y.; Zhou, X.; Lee, KH.; Nakagawa, K.; Niho, S.; Lee, M.; Linke, R. et al. (Jun 2018). "Improvement in Overall Survival in a Randomized Study That Compared Dacomitinib With Gefitinib in Patients With Advanced Non-Small-Cell Lung Cancer and EGFR-Activating Mutations.". J Clin Oncol: JCO2018787994. doi:10.1200/JCO.2018.78.7994. PMID 29864379.
- ↑ Alsharedi, M.; Bukamur, H.; Elhamdani, A. (Jun 2018). "Osimertinib for the treatment of patients with". Drugs Today (Barc) 54 (6): 369-379. doi:10.1358/dot.2018.54.6.2817668. PMID 29998228.