Medical treatment of advanced basal cell carcinoma

被引:0
作者
Basset-Seguin, N. [1 ]
机构
[1] Univ Paris 07, Serv Dermatol, Hop St Louis, Paris, France
来源
ANNALES DE DERMATOLOGIE ET DE VENEREOLOGIE | 2018年 / 145卷
关键词
Advanced BCC; Vismodegib; Sonidegib; Hedgehog pathway; Immunotherapy; DOUBLE-BLIND; HEDGEHOG PATHWAY; HUMAN HOMOLOG; VISMODEGIB; MULTICENTER; RESISTANCE; INHIBITOR; SONIDEGIB; THERAPY; STEVIE;
D O I
暂无
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
Until recently, advanced BCC were only accessible to a highly morbid surgery not necessarily proving to be carcinologic, and leaving terrible dysmorphic sequelae hard to accept by the patient. Another possibility, the only one in case of metastatic BCC, was chemotherapy which efficacy has never been proven in a clinical trial. Radiotherapy is most often not accessible because of previous radiotherapy or because of the localization or the extension of the lesion. The discovery of the importance of the sonic hedgehog pathway in the physiopathology of BCC has opened a new strategy with the development of targeted anti SMO drugs inactivating the pathway. Two molecules have become available following Phase I and II studies: vismodegib (Erivedge (R)) the first in class indicated for locally advanced and metastatic BCC and sonidegib (Odomzo (R)) indicated only for locally advanced BCC. The pharmacokinetic profiles of sonidegib and vismodegib showed several differences. No head to head comparative studies are available between these two drugs. Their pivotal phase II studies had similar study designs and endpoints. The objective response rate (ORR) by central review for vismodegib was 47.6% (95% CI 35.5-60.6) at 21 months follow-up. The ORR for sonidegib according to central review at 18 months follow-up is 56.1% (95% CI 43.3-68.3). Although both treatments share a similar adverse event profile with possible numerically differences in incidence, most patients will discontinue hedgehog inhibitors treatment in the long term because of side effects. Some resistant cases to these drugs have been described but are rather rare. In case of resistance or bad tolerability to the drug future hopes rely on immunotherapy currently under investigation. (C) 2018. Published by Elsevier Masson SAS. All rights reserved.
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收藏
页码:36 / 41
页数:6
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