Galimont-Collen A F S, Vos L E, Lavrijsen A P M, Ouwerkerk J, Gelderblom H
Department of Dermatology, Leiden University Medical Center, P.O. Box 9600, 2300 RC Leiden, The Netherlands.
Eur J Cancer. 2007 Mar;43(5):845-51. doi: 10.1016/j.ejca.2006.11.016. Epub 2007 Feb 7.
Inhibitors of epidermal growth factor receptor (EGFR) are commonly used as therapeutic agents in oncology. In contrast to currently used oncological treatments, these inhibitors almost always cause skin- and skin adnex toxicity. About 85% of treated patients develop to a more or lesser extent an acneiform eruption. Xerosis cutis and painful nail disorders occur in, respectively, 35% and 10-15% of all treated patients. Also hair and mucosal changes have been reported, although to a lesser extent. These skin- and skin adnex toxicities are reversible after withdrawal of treatment, but are seldom a reason to stop or interrupt therapy. This review outlines the classification, the pathogenesis and therapy of these skin, hair, nail and mucosal changes due to EGFR inhibition. Informing the patient and management of these side-effects is very important to reduce discomfort and as such to increase compliance to therapy.
表皮生长因子受体(EGFR)抑制剂在肿瘤学中常用作治疗药物。与目前使用的肿瘤治疗方法不同,这些抑制剂几乎总会引起皮肤及皮肤附属器毒性。约85%接受治疗的患者会不同程度地出现痤疮样皮疹。皮肤干燥和疼痛性甲病分别发生在35%和10 - 15%的所有接受治疗的患者中。也有毛发和黏膜改变的报道,不过程度较轻。这些皮肤及皮肤附属器毒性在停止治疗后是可逆的,但很少成为停止或中断治疗的原因。本综述概述了由于EGFR抑制导致的这些皮肤、毛发、指甲和黏膜改变的分类、发病机制及治疗。告知患者并处理这些副作用对于减轻不适从而提高治疗依从性非常重要。