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预测接受表皮生长因子酪氨酸激酶抑制剂治疗的非小细胞肺癌患者的临床获益情况。

Predicting clinical benefit in non-small-cell lung cancer patients treated with epidermal growth factor tyrosine kinase inhibitors.

作者信息

Amler L C, Goddard A D, Hillan K J

机构信息

Development Sciences, Genentech, Inc., South San Francisco, California 94080, USA.

出版信息

Cold Spring Harb Symp Quant Biol. 2005;70:483-8. doi: 10.1101/sqb.2005.70.048.

Abstract

Erlotinib and gefitinib are small-molecule inhibitors of the epidermal growth factor tyrosine kinase. Erlotinib is approved for the treatment of locally advanced or metastatic non-small-cell lung cancer after failure of at least one prior chemotherapy regimen. Although it is active in unselected patients, clinical characteristics and tumor molecular markers associated with enhanced benefit have been identified. Notably, never-smoker status or a positive EGFR FISH test has been consistently predictive of greater erlotinib benefit. Other markers, such as EGFR mutations and EGFR protein expression, as determined by immunohistochemistry, and KRAS mutation status have not proven to be consistently associated with differential benefit.

摘要

厄洛替尼和吉非替尼是表皮生长因子酪氨酸激酶的小分子抑制剂。厄洛替尼被批准用于治疗在至少一种先前化疗方案失败后的局部晚期或转移性非小细胞肺癌。尽管它在未经过选择的患者中具有活性,但已确定了与增强疗效相关的临床特征和肿瘤分子标志物。值得注意的是,从不吸烟状态或EGFR FISH检测呈阳性一直可预测厄洛替尼有更大疗效。其他标志物,如通过免疫组织化学测定的EGFR突变和EGFR蛋白表达,以及KRAS突变状态,尚未被证明与疗效差异始终相关。

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