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表皮生长因子受体抑制剂作用机制的临床意义

Clinical implications of the mechanism of epidermal growth factor receptor inhibitors.

作者信息

Marshall John

机构信息

Division of Hematology/Oncology, Lombardi Cancer Center, Georgetown University Medical Center, Washington, DC 20007, USA.

出版信息

Cancer. 2006 Sep 15;107(6):1207-18. doi: 10.1002/cncr.22133.

Abstract

Novel therapeutic agents that target the epidermal growth factor receptor (EGFR) constitute an important addition to the therapeutic armamentarium for the treatment of metastatic disease. EGFR-targeted agents currently approved by the U.S. Food and Drug Administration include cetuximab, a monoclonal antibody for the treatment of colorectal cancer; and the small-molecule EGFR tyrosine kinase inhibitor (TKI) erlotinib for the treatment of nonsmall cell lung cancer (NSCLC) and pancreatic cancer. Approval of the TKI gefitinib for NSCLC recently was withdrawn. Although both classes of anti-EGFR agents target the same receptor, substantial distinctions regarding their mechanism significantly affect dosing requirements, toxicity profiles, and their use as combination agents.

摘要

靶向表皮生长因子受体(EGFR)的新型治疗药物是转移性疾病治疗手段的重要补充。美国食品药品监督管理局目前批准的EGFR靶向药物包括用于治疗结直肠癌的单克隆抗体西妥昔单抗;以及用于治疗非小细胞肺癌(NSCLC)和胰腺癌的小分子EGFR酪氨酸激酶抑制剂(TKI)厄洛替尼。TKI吉非替尼用于NSCLC的批准最近已被撤回。尽管这两类抗EGFR药物靶向同一受体,但它们在作用机制上的显著差异对给药要求、毒性特征以及作为联合用药的使用有重大影响。

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