首页> 外文期刊>Clinical colorectal cancer >To give or not to give anti-epidermal growth factor receptor (EGFR) monoclonal antibodies to patients with KRAS G13D mutation in advanced colorectal cancer
【24h】

To give or not to give anti-epidermal growth factor receptor (EGFR) monoclonal antibodies to patients with KRAS G13D mutation in advanced colorectal cancer

机译:为患有晚期大肠癌的KRAS G13D突变的患者提供或不提供抗表皮生长因子受体(EGFR)单克隆抗体

获取原文
获取原文并翻译 | 示例
           

摘要

Recent retrospective analyses of clinical trials in metastatic colorectal cancer reveal a clear lack of efficacy for the anti-epidermal growth factor receptor (EGFR) monoclonal antibodies cetuximab and panitumumab in patients with KRAS mutated tumors. As a result, in 2009 the US Food and Drug Administration updated the labels of cetuximab and panitumumab to exclude treatment of metastatic colorectal cancer with KRAS mutations. However many of these retrospective analyses grouped codon 12 and codon 13 mutations together without subgroup analyses. KRAS mutation frequency in patients with colorectal cancer is approximately 40%, with relative and absolute incidences of the codon G13D mutation of 19.5% and 8%, respectively.3 Different codon mutations have become increasingly important with the arrival of data indicating that perhaps all KRAS mutations are not created equal in terms of their biological effects.
机译:最近对转移性大肠癌临床试验的回顾性分析表明,在患有KRAS突变的肿瘤患者中,抗表皮生长因子受体(EGFR)单克隆抗体西妥昔单抗和帕尼单抗的疗效明显缺乏。结果,2009年,美国食品药品监督管理局更新了西妥昔单抗和帕尼单抗的标签,以排除具有KRAS突变的转移性结直肠癌的治疗。但是,这些回顾性分析中有许多将密码子12和密码子13突变归为一组,而没有进行亚组分析。大肠癌患者的KRAS突变频率约为40%,密码子G13D突变的相对和绝对发生率分别为19.5%和8%。3随着数据的到来,不同的密码子突变变得越来越重要,这表明也许所有KRAS就其生物学效应而言,产生的突变并不相等。

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