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Biomarkers of clinical benefit for anti-epidermal growth factor receptor agents in patients with non-small-cell lung cancer
被引:0
|作者:
A G Pallis
D A Fennell
E Szutowicz
N B Leighl
L Greillier
R Dziadziuszko
机构:
[1] University General Hospital of Heraklion,Department of Medical Oncology
[2] PO Box 1352,Department of Oncology and Radiotherapy
[3] Heraklion 71110,Department of Medical Oncology
[4] Crete,Department of Thoracic Oncology
[5] Greece,undefined
[6] Queen's University Belfast,undefined
[7] Centre for Cancer Research and Cell Biology & Northern Ireland Cancer Centre,undefined
[8] Medical University of Gdansk,undefined
[9] Princess Margaret Hospital,undefined
[10] University of Toronto,undefined
[11] Assistance Publique–Hôpitaux de Marseille,undefined
[12] Faculté de Médecine,undefined
[13] Université de la Méditerranée,undefined
[14] Marseille,undefined
[15] France,undefined
来源:
British Journal of Cancer
|
2011年
/
105卷
关键词:
EGFR;
immunohistochemistry;
gene copy number;
mutations;
gefitinib;
erlotinib;
D O I:
暂无
中图分类号:
学科分类号:
摘要:
Non-small-cell lung cancer (NSCLC) remains by far the major cause of cancer-related death in the Western world in both men and women. The majority of patients will be diagnosed with metastatic disease, and chemotherapy doublets remain the cornerstone of treatment for these patients. However, chemotherapy has a minimal impact on long-term survival and prognosis remains poor for these patients. Further improvement in treatment is likely to require incorporation of novel targeted therapies. Among these agents, inhibitors of the epidermal growth factor receptor (EGFR) have demonstrated significant activity in the first-, second- or third-line treatment of NSCLC. The purpose of current paper is to present the evidence for using several proposed molecular biomarkers as a tool for selection of NSCLC patients for anti-EGFR treatment. According to current data, EGFR mutation status appears to be the strongest predictor for the selection of NSCLC patients to first-line treatment with EGFR tyrosine kinase inhibitors vs chemotherapy. Use of other biomarkers remains investigational.
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页码:1 / 8
页数:7
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