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World J Clin Oncol. Nov 10, 2011; 2(11): 367-376
Published online Nov 10, 2011. doi: 10.5306/wjco.v2.i11.367
Published online Nov 10, 2011. doi: 10.5306/wjco.v2.i11.367
Study | Molecule | Place of study | EGFR positive selectedmutations | No. ofpatients | Clinical stage | Responserate (%) | Median OS(mo) | Median PFS(mo) |
Kris et al, 2003 | Gefitinib | United States | No | 221 | IIIB and IV | 22 | 6-7 | - |
Perez-Soler et al, 2004 | Gefitinib | United States | No | 57 | IIIB and IV | 12.3 | 8.4 | - |
Maemondo et al, 2010 | Gefitinib | Asia | Yes | 230 | IIIB and IV | 73.7 | 30.5 | 10.8 |
Mok et al, 2009 | Gefitinib | Asia | No | 609 | III and IV | 71.2 | 18.6 | 5.7 |
Mitsudomi et al, 2010 | Gefitinib | Japan | yes | 177 | IIIB and IV | 62.1 | 30.9 | 9.2 |
Shepherd et al, 2005 | Erlotinib | America, Europe and Asia | No | 731 | IIIB and IV | 8.9 | 6.7 | 2.2 |
Herbst et al, 2005 | Erlotinib | United States | No | 526 | IIIB and IV | 30 | 10.6 | 6 |
Capuzzo et al, 2010 | Erlotinib | Italy | yes | 437 | IIIB and IV | 11.9 | 12.3 | 12.3 |
- Citation: Mello RA, Marques DS, Medeiros R, Araújo AM. Epidermal growth factor receptor and K-Ras in non-small cell lung cancer-molecular pathways involved and targeted therapies. World J Clin Oncol 2011; 2(11): 367-376
- URL: https://www.wjgnet.com/2218-4333/full/v2/i11/367.htm
- DOI: https://dx.doi.org/10.5306/wjco.v2.i11.367