Cutaneous Toxic Effects Associated With Vemurafenib and Inhibition of the BRAF Pathway

被引:73
作者
Huang, Victor
Hepper, Donna [2 ]
Anadkat, Milan
Cornelius, Lynn [1 ]
机构
[1] Washington Univ, Sch Med, Div Dermatol, Ctr Adv Med, St Louis, MO 63110 USA
[2] Washington Univ, Dept Pathol & Immunol, St Louis, MO 63110 USA
关键词
MULTIKINASE INHIBITOR; KINASE INHIBITORS; TUMOR PROGRESSION; HUMAN CANCER; SORAFENIB; MELANOMA; RAS; MUTATIONS; SPECTRUM; TARGETS;
D O I
10.1001/archdermatol.2012.125
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Background: The development of a novel BRAF inhibitor, vemurafenib, has been associated with impressive tumor regression in patients with BRAF-positive stage IV melanoma. In the phase 3 clinical trials, dermatologic toxic effects associated with vemurafenib were described, namely, the development of eruptive squamous cell carcinomas. Herein, 3 cases are presented that highlight the development of squamous cell carcinomas and other cutaneous sequelae that have not been previously reported and are reminiscent of those observed with administration of the multikinase inhibitor sorafenib tosylate. In addition, the current understanding of the molecular mechanisms underlying these toxic effects is reviewed. Observations: The development of keratosis pilaris-like eruptions; seborrheic dermatitis-like rashes; and hyperkeratotic, tender plantar papules reminiscent of those seen in sorafenib-associated hand-foot skin reaction, as well as squamous cell carcinomas, is presented in association with vemurafenib-based treatment of metastatic melanoma. Conclusions: The development of sorafenib-like cutaneous sequelae (squamous cell carcinomas, keratosis pilaris-like eruptions, seborrheic dermatitis-like rashes, and hand-foot skin reaction) associated with vemurafenib administration suggests that BRAF inhibition alone may be sufficient to induce these changes.
引用
收藏
页码:628 / 633
页数:6
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