Owen Joshua L, Lopez Isha E, Desai Seemal R
J Drugs Dermatol. 2015 May;14(5):509-10.
Vemurafenib, a BRAF inhibitor, is FDA-approved for the treatment of metastatic melanoma in patients who harbor the BRAF V600E mutation. By inhibiting BRAF, vemurafenib prevents the mitogen-activated protein kinase (MAPK) pathway from driving melanoma growth. Here we present a patient with paradoxical activation of the MAPK pathway by vemurafenib, ultimately resulting in deleterious cutaneous manifestations. An emphasis on close follow-up is warranted for new or changing lesions for patients on this medication and other BRAF inhibitors.
维莫非尼是一种BRAF抑制剂,已获美国食品药品监督管理局(FDA)批准,用于治疗携带BRAF V600E突变的转移性黑色素瘤患者。通过抑制BRAF,维莫非尼可防止丝裂原活化蛋白激酶(MAPK)通路驱动黑色素瘤生长。在此,我们报告一名患者,其MAPK通路被维莫非尼反常激活,最终导致有害的皮肤表现。对于正在服用此药物及其他BRAF抑制剂的患者,出现新的或变化的皮损时,有必要加强密切随访。