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表皮生长因子受体突变、基因扩增和蛋白表达与非小细胞肺癌原发和转移肿瘤中的 KRAS 突变及其临床意义:一项荟萃分析。

EGFR mutations, gene amplification, and protein expression and KRAS mutations in primary and metastatic tumors of nonsmall cell lung cancers and their clinical implications: a meta-analysis.

机构信息

Department of Oncology, Shengjing Hospital of China Medical University, China.

出版信息

Cancer Invest. 2011 Nov;29(9):626-34. doi: 10.3109/07357907.2011.621914.

Abstract

A meta-analysis was performed to determine EGFR mutations, gene amplification, and protein expression and KRAS mutations in primary and metastatic nonsmall cell lung cancer (NSCLC). We found that KRAS gene mutation frequencies were higher in primary than in metastatic tumors. There was no significant difference in EGFR mutation frequency between the primary and metastatic tumors. These results suggest that KRAS mutations in primary NSCLC foci may be a more accurate biomarker than in metastases to reflect KRAS mutation status. Combined detection of EGFR and KRAS mutations in primary NSCLC foci appears to be an optimal approach for first-line EGFR-TKI therapy.

摘要

进行了一项荟萃分析,以确定原发性和转移性非小细胞肺癌 (NSCLC) 中的 EGFR 突变、基因扩增和蛋白表达以及 KRAS 突变。我们发现,KRAS 基因突变频率在原发性肿瘤中高于转移性肿瘤。原发性和转移性肿瘤之间 EGFR 突变频率无显著差异。这些结果表明,原发性 NSCLC 病灶中的 KRAS 突变可能比转移灶更能准确反映 KRAS 突变状态,是比转移灶更为准确的生物标志物。在原发性 NSCLC 病灶中联合检测 EGFR 和 KRAS 突变似乎是一线 EGFR-TKI 治疗的最佳方法。

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