Monti M, Motta S
Department of Dermatology, University of Milan and Clinical Institute Humanitas, Milan, Italy.
Int J Biol Markers. 2007 Jan-Mar;22(1 Suppl 4):S53-61.
Cutaneous toxicity is the most evident adverse effect of epidermal growth factor receptor (EGFR) inhibitors because of the specific role played by EGFR in skin biophysiology. Dermatological adverse reactions, mainly folliculocentric, have been widely reported in the literature. However, the mechanism of these reactions is not well defined and their management is still a matter of debate. In this paper keratinocyte differentiation, activation and pathways regulating gene expression are reviewed in order to improve the understanding of adverse skin reactions and obtain success in their management. The authors had the opportunity to treat skin reactions induced by cetuximab in a cohort of patients affected by metastatic colorectal carcinoma. The aims of this clinical approach were to control the signs and symptoms of skin toxicity in order to avoid delay in cancer therapy and to use nondrug agents for the treatment of drug-induced skin reactions.
由于表皮生长因子受体(EGFR)在皮肤生物生理学中发挥的特定作用,皮肤毒性是表皮生长因子受体抑制剂最明显的不良反应。主要以毛囊为中心的皮肤不良反应在文献中已有广泛报道。然而,这些反应的机制尚未明确界定,其处理方法仍存在争议。本文对角质形成细胞的分化、激活及调节基因表达的途径进行综述,以增进对皮肤不良反应的理解并成功处理这些反应。作者有机会治疗一组转移性结直肠癌患者中由西妥昔单抗引起的皮肤反应。这种临床方法的目的是控制皮肤毒性的体征和症状,以避免癌症治疗延迟,并使用非药物制剂治疗药物引起的皮肤反应。