首页> 外文期刊>Oncology: International Journal of Cancer Research and Treatment >Clinical significance of insulin-like growth factor type 1 receptor and epidermal growth factor receptor in patients with advanced gastric cancer.
【24h】

Clinical significance of insulin-like growth factor type 1 receptor and epidermal growth factor receptor in patients with advanced gastric cancer.

机译:胰岛素样生长因子1型受体和表皮生长因子受体在晚期胃癌患者中的临床意义。

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

OBJECTIVE: To better understand the clinical implications of insulin-like growth factor type 1 receptor (IGF-1R), epidermal growth factor receptor (EGFR) and HER2 expressions in gastric cancer (GC). METHODS: The study group comprised 86 patients who received first-line chemotherapy for advanced GC at the National Cancer Center Hospital. Using laser-captured microdissection and a real-time RT-PCR assay, we quantitatively evaluated mRNA levels of IGF-1R, EGFR and HER2 in paraffin-embedded cancer specimens of surgically removed primary tumors. RESULTS: In univariate analysis of the study group as a whole, patients with low expression of both IGF-1R and EGFR (n = 13) had a significantly longer overall survival than the other patients (n = 51; median, 24.6 vs. 12.8 months; log-rank p = 0.013). Multivariate survival analysis demonstrated that high EGFR expression [hazard ratio, HR: 2.94 (95% confidence interval, CI: 1.40-6.17), p = 0.004] and poor performance status [HR: 1.96 (95% CI: 1.12-3.42), p = 0.018] were significant predictors of poor survival. In patients given first-line S-1 monotherapy (n = 29), low IGF-1R (p = 0.002) and low EGFR (p = 0.035) gene expression correlated with a better response, without a significant prolongation of survival. CONCLUSION: Our data warrant further investigations on the strategy of co-targeting IGF-1R and EGFR in GC.
机译:目的:为了更好地了解胰岛素样生长因子1型受体(IGF-1R),表皮生长因子受体(EGFR)和HER2在胃癌(GC)中的临床意义。方法:研究组包括86例在国家癌症中心医院接受一线化疗以进行晚期GC的患者。使用激光捕获显微解剖和实时RT-PCR分析,我们定量评估了手术切除的原发性肿瘤石蜡包埋的癌症样本中IGF-1R,EGFR和HER2的mRNA水平。结果:在整个研究组的单因素分析中,IGF-1R和EGFR表达均低的患者(n = 13)比其他患者(n = 51;中位值分别为24.6和12.8)长得多。月;对数排名p = 0.013)。多变量生存分析表明,EGFR表达高[风险比,HR:2.94(95%置信区间,CI:1.40-6.17),p = 0.004]和较差的状态[HR:1.96(95%CI:1.12-3.42), p = 0.018]是生存不良的重要预测指标。在接受一线S-1单药治疗的患者(n = 29)中,低IGF-1R(p = 0.002)和低EGFR(p = 0.035)基因表达与较好的反应相关,且无明显延长生存期。结论:我们的数据值得进一步研究在GC中共同靶向IGF-1R和EGFR的策略。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号