...
首页> 外文期刊>Future oncology >Cabozantinib (XL184) for the treatment of locally advanced or metastatic progressive medullary thyroid cancer
【24h】

Cabozantinib (XL184) for the treatment of locally advanced or metastatic progressive medullary thyroid cancer

机译:卡波替尼(XL184)用于治疗局部晚期或转移性进行性甲状腺髓样癌

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Cabozantinib (XL184) is an oral multiple receptor tyrosine kinase inhibitor manufactured by Exelixis Inc., CA, USA. It mainly inhibits three tyrosine kinase receptors: MET, VEGFR2 and RET. In both preclinical and clinical studies it has been shown to inhibit tumor angiogenesis, invasiveness and metastases. The most frequent side effects are fatigue, diarrhea, decreased appetite, nausea, weight loss and palmar-plantar erythrodysesthesia. A Phase III clinical trial (EXAM study) of XL184 versus placebo in advanced and progressive medullary thyroid cancer showed a 28 versus 0% overall response rate and a progression-free survival of 11.2 versus 4.0 months (hazard ratio: 0.28; 95% CI: 0.19-0.40; p < 0.0001) in patients treated with cabozantinib and placebo, respectively. The drug has been approved by the US FDA for the treatment of advanced/progressive metastatic medullary thyroid cancer in the USA. The EMA is now evaluating its approval in Europe.
机译:Cabozantinib(XL184)是美国加利福尼亚州Exelixis Inc.生产的口服多受体酪氨酸激酶抑制剂。它主要抑制三种酪氨酸激酶受体:MET,VEGFR2和RET。在临床前和临床研究中,它均能抑制肿瘤血管生成,侵袭性和转移。最常见的副作用是疲劳,腹泻,食欲下降,恶心,体重减轻和掌-红斑感觉不良。 XL184与安慰剂治疗晚期和进行性甲状腺髓样癌的III期临床试验(EXAM研究)显示总缓解率分别为28%和0%,无进展生存期为11.2和4.0个月(危险比:0.28; 95%CI:分别用卡博替尼和安慰剂治疗的患者0.19-0.40; p <0.0001)。该药物已获得美国食品药品管理局(FDA)的批准,可在美国用于治疗晚期/进行性转移性甲状腺髓样癌。 EMA现在正在评估其在欧洲的批准。

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