Department of Dermatology, Nantes University Hospital, 1 place Alexis Ricordeau, 44093 Nantes Cedex 1, France
CRCNA, INSERM U892, CNRS 6299, 9 Quai Moncousu, 44093 Nantes, France
Eur J Dermatol. 2022 May 1;32(3):401-407. doi: 10.1684/ejd.2022.4264.
Vismodegib is indicated for the treatment of advanced or metastatic basal cell carcinoma (BCC). The predictive factors of response to vismodegib have so far been poorly described.
The primary objective was to determine the profile of patients responding to vismodegib and the duration of response. Secondary objectives were to assess whether there is a correlation between the duration of treatment and the risk of relapse, and to define factors associated with relapse.
MATERIALS & METHODS: We included 61 patients with locally advanced BCC (laBCC) or multiple BCC, treated with vismodegib (150 mg per day), from July 2011 to November 2015, in the Oncodermatology Department of Nantes University Hospital in France. Tumour response was assessed using Response Evaluation Criteria in Solid Tumours version 1.1.
Thirty-nine patients had advanced BCC (64%) and 22 patients multiple BCC (36%), including 10 patients with Gorlin syndrome. No factor predicted response to vismodegib. The median progression-free survival (PFS) was 69.5 months for the total population. In multivariate analysis, multiple BCC was the only factor associated with an increased risk of relapse (HR: 13.80 [CI95%, 1.93-98.64, p < 0.01]). Treatment duration decreased the risk of relapse (HR 0.95 [CI95%, 0.90-0.99, p = 0.0467]). Among the 20 patients who experienced relapse during follow-up, 15 (75%) were re-treated with vismodegib, with a response rate of 66%.
Although we were unable to establish predictive factors for the response to vismodegib, we demonstrate for the first time that increased treatment duration correlates with a decreased risk of relapse.
维莫德吉适用于治疗晚期或转移性基底细胞癌(BCC)。迄今为止,其反应的预测因素描述得还不够完善。
主要目的是确定对维莫德吉有反应的患者特征和反应持续时间。次要目的是评估治疗持续时间与复发风险之间是否存在相关性,并确定与复发相关的因素。
我们纳入了 2011 年 7 月至 2015 年 11 月在法国南特大学医院肿瘤皮肤科接受维莫德吉(每日 150mg)治疗的 61 例局部晚期 BCC(laBCC)或多发性 BCC 患者。使用实体瘤反应评价标准 1.1 评估肿瘤反应。
39 例患者患有晚期 BCC(64%),22 例患者患有多发性 BCC(36%),包括 10 例 Gorlin 综合征患者。没有因素可预测维莫德吉的反应。总人群的无进展生存期(PFS)中位数为 69.5 个月。多变量分析显示,多发性 BCC 是唯一与复发风险增加相关的因素(HR:13.80[95%CI,1.93-98.64,p<0.01])。治疗持续时间降低了复发风险(HR 0.95[95%CI,0.90-0.99,p=0.0467])。在随访期间经历复发的 20 例患者中,15 例(75%)接受了维莫德吉的再治疗,反应率为 66%。
尽管我们无法确定维莫德吉反应的预测因素,但我们首次证明,增加治疗持续时间与降低复发风险相关。