"Who should receive epidermal growth factor receptor inhibitors for non-small cell lung cancer and when?"

被引:20
作者
Hann C.L. [1 ]
Brahmer J.R. [1 ]
机构
[1] The Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins, Baltimore, MD 21231-1000
关键词
Epidermal Growth Factor Receptor; Erlotinib; Epidermal Growth Factor Receptor Mutation; Epidermal Growth Factor Receptor Inhibitor; Epidermal Growth Factor Receptor Gene;
D O I
10.1007/s11864-007-0024-2
中图分类号
学科分类号
摘要
Inhibition of the epidermal growth factor receptor (EGFR) pathway in non-small cell lung cancer (NSCLC) is an exciting and rapidly evolving field. Erlotinib and gefitinib, two tyrosine kinase inhibitors (TKIs) of EGFR, have demonstrated activity in advanced NSCLC in the second- and third-line settings. Subset analyses of phase II and phase III clinical trials lead to the recognition that these two agents had more activity in certain subsets of NSCLC patients including never smokers, people of Asian descent and patients with EGFR FISH-positive or mutation-positive tumors. In particular, never smokers had statistically significant improvements in survival with either erlotinib or gefitinib therapy. Patients with EGFR FISH- or mutation-positive tumors had improved response rates to TKI therapy while those with KRAS mutant tumors did not derive any benefit. In the BR.21 trial treatment with erlotinib resulted in statistically significant improvements in overall survival and quality of life. Thus, while the question of who should receive EGFR TKI therapy is still not completely answered, all patients should be considered for erlotinib therapy in the second- or third-line setting. In daily clinical practice, there is currently no data to support the use of EGFR mutation or FISH status in this decision making process. Prospective trials are ongoing to determine which patient and tumor characteristics are predictive of a clinical benefit from TKI therapy. © Springer Science+Business Media, LLC 2007.
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页码:28 / 37
页数:9
相关论文
共 59 条
[51]  
Cappuzzo F., Hirsch F.R., Rossi E., Et al., Epidermal growth factor receptor gene and protein and gefitinib sensitivity in non-small-cell lung cancer, J Natl Cancer Inst, 97, pp. 643-655, (2005)
[52]  
Cappuzzo F., Toschi L., Trisolini R., Et al., Clinical and biological effects of gefitinib in EGFR RISH+/Phospho-Akt+ or never smoker non-small cell lung cancer (NSCLC): Preliminary results of the ONCOBELL trial, J Clin Oncol, 24, (2006)
[53]  
Ahrendt S.A., Decker P.A., Alawi E.A., Et al., Cigarette smoking is strongly associated with mutation of the K-ras gene in patients with primary adenocarcinoma of the lung, Cancer, 92, pp. 1525-1530, (2001)
[54]  
Pao W., Wang T.Y., Riely G.J., Et al., KRAS mutations and primary resistance of lung adenocarcinomas to gefitinib or erlotinib, PLoS Med, 2, (2005)
[55]  
Thomas S.K., Fossella F.V., Liu D., Et al., Asian ethnicity as a predictor of response in patients with non-small-cell lung cancer treated with gefitinib on an expanded access program, Clin Lung Cancer, 7, pp. 326-331, (2006)
[56]  
Ho C., Murray N., Laskin J., Et al., Asian ethnicity and adenocarcinoma histology continues to predict response to gefitinib in patients treated for advanced non-small cell carcinoma of the lung in North America, Lung Cancer, 49, pp. 225-231, (2005)
[57]  
Chen Y.M., Perng R.P., Tsai C.M., Gefitinib treatment is highly effective in non-small-cell lung cancer patients failing previous chemotherapy in Taiwan: A prospective phase II study, J Chemother, 17, pp. 679-684, (2005)
[58]  
Lee D.H., Han J.Y., Kim H.T., Lee J.S., Gefitinib is of more benefit in chemotherapy-naive patients with good performance status and adenocarcinoma histology: Retrospective analysis of 575 Korean patients, Lung Cancer, 53, pp. 339-345, (2006)
[59]  
Clark G.M., Zborowski D.M., Santabarbara P., Et al., Smoking history and epidermal growth factor receptor expression as predictors of survival benefit from erlotinib for patients with non-small-cell lung cancer in the National Cancer Institute of Canada Clinical Trials Group study BR.21, Clin Lung Cancer, 7, pp. 389-394, (2006)