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临床试验/NCT04089748
NCT04089748已完成不适用

Basal Tumours in Bladder Cancer, Response to chemoTherapy

University Hospital, Rouen1 个研究点 分布在 1 个国家目标入组 293 人开始时间: 2019年2月27日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
293
试验地点
1
主要终点
Identifying mechanisms of resistance in basal subgroups.

研究概览

简要总结

Determine the sensitivity/resistance to chemotherapy of the various subgroups of muscle-invasive bladder cancers, including the basal subgroup (about 25% of these tumours) according to 4 different classifications based on molecular or immunohistochemical classifiers.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 未提供

排除标准

  • Patients enrolled in VESPER study:Tumors from patient having withdrawn his/her informed consent form for the participation to the collection and/or VESPER project.
  • Patients from St Louis not enrolled in VESPER study:Tumors from patient having expressed opposition against research program after 1 month for the participation to the collection.

结局指标

主要结局

Identifying mechanisms of resistance in basal subgroups.

时间窗: through study completion, an average of 3 years

Identifying molecular subgroups of bladder cancer patients within VESPER and Saint-Louis cohort, who could benefit from neoadjuvant chemotherapy, taking into account the existence of different classification systems.

时间窗: through study completion, an average of 3 years

Determining which classification(s) has(ve) the best ability to identifying subgroups of tumours sensitive or resistant to neoadjuvant chemotherapy.

时间窗: through study completion, an average of 3 years

次要结局

未报告次要终点

研究者

发起方
University Hospital, Rouen
申办方类型
Other
责任方
Sponsor

研究点 (1)

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