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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.
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页码:353 / 365
页数:13
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