Olivia Newton-John Cancer Research Institute, Melbourne, VIC, Australia.
School of Cancer Medicine, La Trobe University, Bundoora, VIC, Australia.
Br J Cancer. 2018 Apr;118(7):966-971. doi: 10.1038/s41416-018-0021-1. Epub 2018 Mar 12.
Advanced biliary tract cancers (BTCs) have a poor prognosis and limited treatment options. This exploratory phase II study aimed to evaluate the activity of the mTOR inhibitor everolimus in advanced BTC and explore prognostic biomarkers.
Patients with advanced BTCs, who had not received chemotherapy for advanced disease, were enroled to receive everolimus (10 mg daily). The primary endpoint was disease control rate (DCR) at 12 weeks. Secondary endpoints included overall response rate, progression-free survival (PFS), overall survival (OS) and adverse events. Activation status of the RAS and phosphatidylinositol 3-kinase (PI3K)/AKT/mTOR pathways was assessed by DNA sequencing and immunohistochemistry on archival tumour tissue.
The study enroled 27 patients and the DCR at 12 weeks was 48%. Median PFS was 5.5 months (95% confidence interval (CI): 2.1-10.0 months) and median OS was 9.5 months (95% CI: 5.5-16.6 months). DCR at 12 weeks was significantly worse for gall bladder carcinoma compared to other anatomical sites, and there was a trend towards a worsened PFS and OS. Treatment was well tolerated. KRAS (12%) and PIK3CA mutations (12%) were uncommon. Immunohistochemical staining for PI3K/AKT/mTOR pathways did not significantly correlate with outcome.
In unselected patients, everolimus demonstrated clinical activity as first-line monotherapy in advanced BTC.
晚期胆道癌(BTC)预后较差,治疗选择有限。本探索性 II 期研究旨在评估 mTOR 抑制剂依维莫司在晚期 BTC 中的疗效,并探索预后生物标志物。
本研究招募了未接受过晚期疾病化疗的晚期 BTC 患者,给予依维莫司(每日 10mg)治疗。主要终点为 12 周时的疾病控制率(DCR)。次要终点包括总缓解率、无进展生存期(PFS)、总生存期(OS)和不良事件。通过 DNA 测序和对存档肿瘤组织的免疫组化检测,评估 RAS 和磷脂酰肌醇 3-激酶(PI3K)/AKT/mTOR 通路的激活状态。
本研究共纳入 27 例患者,12 周时 DCR 为 48%。中位 PFS 为 5.5 个月(95%置信区间[CI]:2.1-10.0 个月),中位 OS 为 9.5 个月(95%CI:5.5-16.6 个月)。与其他解剖部位相比,胆囊癌的 12 周 DCR 显著较差,且 PFS 和 OS 均有恶化趋势。治疗耐受性良好。KRAS(12%)和 PIK3CA 突变(12%)较为少见。PI3K/AKT/mTOR 通路的免疫组化染色与结局无显著相关性。
在未选择的患者中,依维莫司作为晚期 BTC 的一线单药治疗具有临床活性。