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首页> 外文期刊>Clinical advances in hematology & oncology: H&O >LUX-Lung 3: A Randomized, Open-Label, Phase III Study of Afatinib Versus Pemetrexed and Cisplatin as First-Line Treatment for Patients With Advanced Adenocarcinoma of the Lung Harboring EGFR-Activating Mutations
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LUX-Lung 3: A Randomized, Open-Label, Phase III Study of Afatinib Versus Pemetrexed and Cisplatin as First-Line Treatment for Patients With Advanced Adenocarcinoma of the Lung Harboring EGFR-Activating Mutations

机译:LUX-Lung 3:一项随机、非盲、第三阶段研究Afatinib与培美曲塞和顺铂作为患者的一线治疗先进的肺腺癌窝藏EGFR-Activating突变

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摘要

James C. Yang, MD, presented the LUX-Lung 3 study, which is a randomized, open-label, phase III trial of afatinib versus cisplatin and pemetrexed as first-line treatment for patients with advanced adenocarcinoma of the lung harboring mutations that activate the EGFR. Afatinib is an irreversible ErbB family blocker.Afatinib differs from the reversible EGFR tyrosine kinase inhibitors (TKIs) gefi-tinib and erlotinib in that after it enters the cell, it covalently binds to the cys-teine residue of EGFR. This provides long inhibition of EGFR. Afatinib also inhibits other ErbB family receptor heterodimers, such as human epidermal growth factor receptor (HER) 2, HER3, and HER4. Additionally, afatinib has in vitro activity against the EGFR-resistant T790M mutation.
机译:詹姆斯·c·杨,医学博士LUX-Lung 3的研究中,这是一个随机、非盲、第三阶段审判afatinib与顺铂及培美曲塞作为患者的一线治疗先进的肺腺癌窝藏激活表皮生长因子受体突变。不可逆ErbB家族拦截器。可逆的表皮生长因子受体酪氨酸激酶抑制剂(TKIs) gefi-tinib埃罗替尼它进入细胞后,共价结合EGFR的cys-teine残渣。提供长期抑制表皮生长因子受体。抑制其他ErbB家族受体形成,人类表皮生长因子受体等(她)2、HER3 HER4。体外对EGFR-resistant活动吗T790M突变。

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