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临床试验/NCT03612232
NCT03612232进行中(未招募)2 期

A Multicenter, Open-label, Phase II Study to Evaluate the Efficacy and Safety of Cabozantinib in Advanced (Unresectable or Metastatic) Adrenocortical Carcinoma

Wuerzburg University Hospital2 个研究点 分布在 1 个国家目标入组 37 人开始时间: 2019年6月4日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
进行中(未招募)
入组人数
37
试验地点
2
主要终点
progression free survival at 4 months

研究概览

简要总结

Adrenocortical carcinoma is an orphan malignant disease that has a dismal prognosis in advanced stages. Mitotane is the only approved treatment but is limited by severe toxicity. Efficacy of mitotane is unsatisfactory with an objective response rate of ≈20% in monotherapy in selected patients (Megerle et al., JCEM 2018). Cytotoxic chemotherapy with etoposide, doxorubin and cisplatin (EDP) or streptozotocin (Sz) in addition to mitotane (Fassnacht et al., N Engl J Med 2012) succeeded in a progression-free survival of 5.6 months and 2.2 months, respectively in patients with advanced ACC. Objective response rates were 23 and 9%. EDP plus mitotane is therefore considered as standard treatment of ACC. Results by Phan et al. (Cancer Research 2015) demonstrated expression of c-MET and its ligand HGF in ACC and provide a rationale to therapeutically target c-MET in ACC. In a case series of 16 patients with advanced ACC refractory to mitotane (with the exception of one case) and 3 (median, range 0-8)further lines of therapy, single agent treatment with cabozantinib off label resulted in three partial responses and five additional cases of disease stabilization for four months or longer (Kroiss et al., J Clin Endocrinol Metab 2020).

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究组 & 干预措施

Cabozantinib

Experimental

oral cabozantinib as tablets continuously (60 mg single dose, tablets)

干预措施: Cabozantinib-s-malate (Drug)

结局指标

主要结局

progression free survival at 4 months

时间窗: 4 months

次要结局

  • overall survival(12 months)
  • best percentage change in size of target lesions(12 months)
  • treatment emergent adverse events (CTC-AE 4.03)(12 months)
  • Objective Response Rates (ORR)(12 months)
  • progression-free survival(12 months)
  • quality of life by EORTC QLQ-C30(12 months)
  • Duration of response (DR)(12 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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