Department of Medicine, Roswell Park Cancer Institute, Buffalo, New York.
Curr Oncol. 2010 Jul;17 Suppl 1(Suppl 1):S18-30. doi: 10.3747/co.v17is1.615.
The epidermal growth factor receptor (EGFR), a member of the ErbB family of receptor tyrosine kinases, plays an important role in the control of cell growth and differentiation. Disruption of its signaling leads to neoplastic cell proliferation, migration, stromal invasion, resistance to apoptosis, and angiogenesis.EGFR is overexpressed in a variety of solid tumors, including colorectal cancer (CRC), and its overexpression is associated with poorer prognosis. One class of agents that is currently used to target EGFR in the treatment of metastatic CRC (mCRC) is the monoclonal antibodies. While the monoclonal antibody EGFR inhibitors lack many of the severe side effects commonly observed with cytotoxic chemotherapy, they are associated with a set of unique dermatological toxicities. This paper reviews the safety profile of the anti-EGFR monoclonal antibodies cetuximab and panitumumab in the treatment of mCRC.
表皮生长因子受体(EGFR)是受体酪氨酸激酶 ErbB 家族的一员,在控制细胞生长和分化方面发挥着重要作用。其信号通路的异常会导致肿瘤细胞的增殖、迁移、基质浸润、抗凋亡和血管生成。EGFR 在多种实体瘤中过度表达,包括结直肠癌(CRC),其过度表达与预后不良相关。目前用于治疗转移性结直肠癌(mCRC)的靶向 EGFR 的一类药物是单克隆抗体。虽然 EGFR 单克隆抗体抑制剂缺乏许多与细胞毒性化疗常见的严重副作用,但它们与一组独特的皮肤毒性相关。本文综述了抗 EGFR 单克隆抗体西妥昔单抗和帕尼单抗在 mCRC 治疗中的安全性特征。