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Clinical Efficacy and Toxicity of Anti-EGFR Therapy in Common Cancers

机译:抗EGFR治疗常见癌症的临床疗效和毒性

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Epidermal growth factor receptor (EGFR) is a cell surface molecule and member of the ErbB family of receptor tyrosine kinases. Its activation leads to proliferation, antiapoptosis, and metastatic spread, making inhibition of this pathway a compelling target. In recent years, an increasing number of clinical trials in the management of solid malignancies have become available indicating the clinical efficacy of anti-EGFR monoclonal antibodies and oral small molecule tyrosine kinase inhibitors (TKIs). This review addresses frequently used EGFR inhibitors, summarizes clinical efficacy data of these new therapeutic agents, and discusses their associated toxicity and management.
机译:表皮生长因子受体(EGFR)是细胞表面分子,是受体酪氨酸激酶ErbB家族的成员。它的激活导致增殖,抗凋亡和转移扩散,使对该途径的抑制成为引人注目的靶标。近年来,越来越多的关于治疗实体恶性肿瘤的临床试验表明抗EGFR单克隆抗体和口服小分子酪氨酸激酶抑制剂(TKI)的临床疗效。这篇综述针对常用的EGFR抑制剂,总结了这些新治疗剂的临床疗效数据,并讨论了其相关的毒性和治疗方法。

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