Sussex Eye Hospital, Brighton Sussex University Hospital, Eastern Road, Brighton, BN2 5BF, UK.
Brighton and Sussex Medical School, Falmer, Brighton, BN1 9PX, UK.
Eye (Lond). 2020 Nov;34(11):2076-2081. doi: 10.1038/s41433-020-0778-3. Epub 2020 Jan 29.
Vismodegib (Erivedge, Genentech) is a first-in-class inhibitor of the hedgehog (Hh) pathway, which is licensed for use in locally advanced basal cell carcinoma (BCC) and metastatic BCC. The National Institute for Health and Care Excellence withdrew recommendation for use of vismodegib secondary to a lack of data comparing vismodegib to standard supportive care. The purpose of this multicentre, international case series is to report outcomes of patients with locally advanced periocular BCC who have been treated with vismodegib.
The medical records of all patients treated with vismodegib were retrospectively reviewed across seven institutions in the United Kingdom, Australia, and New Zealand.
Thirteen patients were identified. Seven (54%) patients were male. All BCCs were ill-defined, with seven (58%) having orbital involvement at presentation. Median treatment time was 7 months (range 2-36 months). Eleven out of 13 patients developed side effects, the most common being fatigue in six patients (46%). Median follow-up was 24 months (range 12-48 months). Complete response was found in 5/13 patients (38%) and a partial response in 8/13 patients (62%). Six patients had further surgery after vismodegib, with three classed as globe-sparing operations. Three patients developed recurrence (23%). Three patients (23%) ultimately underwent exenteration.
This study demonstrates vismodegib to be a well-tolerated treatment which may, in some cases, facilitate globe-sparing surgery and hence avoid disfiguring operations such as exenteration. Uncertainty does remain regarding the long-term outcomes of patients treated with vismodegib.
维莫德吉(Erivedge,罗氏)是一种新型的 Hedgehog(Hh)通路抑制剂,被批准用于局部晚期基底细胞癌(BCC)和转移性 BCC。由于缺乏维莫德吉与标准支持性护理比较的数据,国家卫生与保健卓越研究所(NICE)撤回了对维莫德吉的使用建议。本多中心、国际病例系列研究旨在报告局部晚期眶周 BCC 患者接受维莫德吉治疗的结果。
回顾性分析了英国、澳大利亚和新西兰的 7 家机构中接受维莫德吉治疗的所有患者的病历。
共确定了 13 名患者。7 名(54%)为男性。所有 BCC 边界不清,7 名(58%)患者在初诊时即有眼眶受累。中位治疗时间为 7 个月(范围 2-36 个月)。13 名患者中有 11 名(85%)发生了副作用,最常见的是 6 名患者(46%)出现疲劳。中位随访时间为 24 个月(范围 12-48 个月)。完全缓解者 5 例(38%),部分缓解者 8 例(62%)。维莫德吉治疗后有 6 名患者进一步手术,其中 3 名患者为保眼球手术。3 名患者(23%)复发。3 名患者(23%)最终接受了眶内容剜除术。
本研究表明维莫德吉是一种耐受性良好的治疗方法,在某些情况下,可能有助于保眼球手术,从而避免了毁容性手术,如眶内容剜除术。对于接受维莫德吉治疗的患者的长期结局仍存在不确定性。