Vismodegib: A Review in Advanced Basal Cell Carcinoma

被引:74
作者
Frampton, James E. [1 ]
Basset-Seguin, Nicole [2 ]
机构
[1] Springer, Private Bag 65901, Auckland 0754, New Zealand
[2] Univ Paris 07, Hop St Louis, Dept Dermatol, Paris, France
关键词
HEDGEHOG PATHWAY INHIBITOR; (VISMO)-RELATED ADVERSE EVENTS; DRUG-RESISTANCE; PHARMACOKINETICS; MANAGEMENT; SAFETY; THERAPY; RISK; SONIDEGIB; GDC-0449;
D O I
10.1007/s40265-018-0948-9
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Vismodegib (Erivedge(A (R))) is the first-in-class, oral small molecule inhibitor of the Hedgehog (Hh) pathway, abnormal activation of which is associated with basal cell carcinoma (BCC). In the USA, vismodegib is indicated for the treatment of adults with metastatic BCC (mBCC) or with locally-advanced BCC (LaBCC) that has recurred following surgery or who are not candidates for surgery, and who are not candidates for radiation. Similarly, in the EU, vismodegib is indicated for the treatment of adult patients with symptomatic mBCC, or with laBCC inappropriate for surgery or radiotherapy. The full European approval of vismodegib was based on the results of two phase II, open-label, noncomparative, international trials (ERIVANCE BCC and STEVIE), both of which showed high rates of tumour control in the indicated patient populations, including individuals with or without Gorlin syndrome. These studies also showed that vismodegib has an acceptable and manageable tolerability profile characterized by a number of class-related treatment-emergent adverse events, including muscle spasms, taste disturbances, alopecia, weight loss and asthenia (fatigue). Primary and secondary resistance to vismodegib has been documented, albeit at a low rate compared with some other targeted therapies. Vismodegib is therefore an effective and generally well tolerated systemic therapy for patients with mBCC and laBCC that can no longer be suitably controlled with surgery and/or radiotherapy. Historically, it is the first member of a class of drugs (Hh pathway inhibitors) that are now considered to be first-line treatment options for such individuals.
引用
收藏
页码:1145 / 1156
页数:12
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