Emerging drugs and combination strategies for basal cell carcinoma

被引:20
|
作者
Dreier, Jil [1 ]
Dummer, Reinhard [1 ]
Felderer, Lea [1 ]
Naegeli, Mirjam [1 ]
Gobbi, Sharon [1 ]
Kunstfeld, Rainer [2 ]
机构
[1] Univ Zurich Hosp, Dept Dermatol, CH-8091 Zurich, Switzerland
[2] Univ Hosp Vienna, Dept Dermatol, A-1090 Vienna, Austria
关键词
adverse events; basal cell carcinoma; combination therapy; Hedgehog inhibitors; resistance; side effects; smoothened inhibitors; sonidegib; toxic myopathy; HEDGEHOG PATHWAY INHIBITOR; NONMELANOMA SKIN-CANCER; CUTANEOUS SQUAMOUS-CELL; GROWTH-FACTOR RECEPTOR; SMALL-MOLECULE RITA; SIGNALING PATHWAY; INTRALESIONAL INTERFERON-ALPHA-2B; ACQUIRED-RESISTANCE; MICRORNA EXPRESSION; DOSE-ESCALATION;
D O I
10.1517/14728214.2014.914171
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Basal cell carcinoma (BCC) is a malignancy that is driven by an activated Hedgehog (Hh) pathway. Smoothened inhibitors are a new promising treatment option for patients with locally advanced or metastatic BCC or basal cell nevus syndrome. But long-term data are still limited, the optimal treatment duration is not yet defined and there are already documented cases with acquired resistance. Areas covered: Treatment modalities with Hh inhibitors, side effects and potential pharmacological combination options are discussed. The current literature, including PubMed, Cochrane database and registered trials on ClinicalTrials.gov, was searched. Expert opinion: BCCs typically regress during therapy with Hh inhibitors. Muscle toxicity, dysgeusia and hair loss can be considered as on target adverse reactions. Muscle toxicity is the dose-limiting toxicity of sonidegib. It was not seen with vismodegib because of its high binding to plasma protein alpha-1-acid glycoprotein. Sonidegib is different and shows a clear dose-toxicity relationship, which allows to address the question of whether there is a dose dependency of regression rate, cure rate and progression-free survival. In addition, basic research has offered strategies to enhance efficacy by the combination with other molecules, such as EGFR inhibitors, MEK inhibitors or immunotherapy.
引用
收藏
页码:353 / 365
页数:13
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