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未经酪氨酸激酶抑制剂治疗的非小细胞肺癌中原发肿瘤与相应转移瘤之间表皮生长因子受体突变的比较。

Comparison of epidermal growth factor receptor mutations between primary and corresponding metastatic tumors in tyrosine kinase inhibitor-naive non-small-cell lung cancer.

作者信息

Gow C-H, Chang Y-L, Hsu Y-C, Tsai M-F, Wu C-T, Yu C-J, Yang C-H, Lee Y-C, Yang P-C, Shih J-Y

机构信息

Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan.

出版信息

Ann Oncol. 2009 Apr;20(4):696-702. doi: 10.1093/annonc/mdn679. Epub 2008 Dec 16.

Abstract

BACKGROUND

Mutations of the epidermal growth factor receptor (EGFR) gene in non-small-cell lung cancer (NSCLC) patients predict the patients who will respond to EGFR tyrosine kinase inhibitor (TKI) treatment. A recent study has suggested that 33% of NSCLC showed primary tumor/metastasis discordance of EGFR expression by immunohistochemistry analysis. We intended to find out whether the EGFR mutations of primary lung cancers are concordant to that of corresponding metastatic tumors.

MATERIALS AND METHODS

We analyzed EGFR exons 18-21 from paired primary and metastatic tumors in 67 lung cancer patients who had not received TKI before tissues were sampled.

RESULTS

Using the direct sequencing method, 9 of 18 (50%) patients with EGFR mutation-positive primary lung tumors had lost the mutations in metastases. For 26 patients who were EGFR mutation positive in the metastatic tumors, 17 (65%) were negative in the primary tumors. We analyzed these paired tissues with discrepant EGFR mutations by the Scorpion Amplified Refractory Mutation System assay. Finally, the discordant rate reached 27% (18 of 67 cases).

CONCLUSION

EGFR mutations in primary lung tumors do not always reflect the same situation in metastases. Analysis of EGFR mutations in the primary lung tumor would be inadequate for planning the use of TKI for advanced NSCLC.

摘要

背景

非小细胞肺癌(NSCLC)患者的表皮生长因子受体(EGFR)基因突变可预测患者对EGFR酪氨酸激酶抑制剂(TKI)治疗的反应。最近一项研究表明,通过免疫组化分析,33%的NSCLC存在原发性肿瘤/转移灶EGFR表达不一致的情况。我们旨在探究原发性肺癌的EGFR突变与相应转移瘤的EGFR突变是否一致。

材料与方法

我们分析了67例未接受过TKI治疗的肺癌患者配对的原发性和转移性肿瘤组织中的EGFR第18 - 21外显子。

结果

采用直接测序法,18例EGFR突变阳性的原发性肺癌患者中有9例(50%)在转移灶中失去了这些突变。对于26例转移瘤中EGFR突变阳性的患者,17例(65%)原发性肿瘤为阴性。我们通过蝎形扩增难治性突变系统检测分析了这些EGFR突变不一致的配对组织。最终,不一致率达到27%(67例中的18例)。

结论

原发性肺癌中的EGFR突变并不总是反映转移灶中的相同情况。分析原发性肺癌中的EGFR突变对于晚期NSCLC使用TKI的治疗规划是不够的。

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