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临床试验/NCT02841865
NCT02841865已完成不适用

Evaluation of Radiological Response of Pancreatic Neuroendocrine Tumors: Comparison Between the Choi and the RECIST Criteria

Grupo Espanol de Tumores Neuroendocrinos10 个研究点 分布在 1 个国家目标入组 104 人开始时间: 2015年7月24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
104
试验地点
10
主要终点
Response to treatment

研究概览

简要总结

The Response Evaluation Criteria in Solid Tumors (RECIST), based on differences in tumor size, has been considered as a reproducible method that facilitates not only the measurement of the mass but the evaluation of response to given treatments; while classic chemotherapy induces a reduction of the tumor, new target therapies frequently produce the stabilization of the disease or a delayed progression. These new therapeutic alternatives have shade light on the limitations of the RECIST criteria, since the response to these type of treatments are basically associated with changes on the radiological characteristics of the tumor, as well as other findings in functional imaging.

This study is aimed to compare the response rates according both Choi and RECIST criteria.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Cross Sectional

入排标准

性别
All
接受健康志愿者
否

入选标准

  • •Patients with a pancreatic neuroendocrine tumor with a Ki67 index <20%, who accept to participate and sign the consent form. In case of death patients, waiver of consent has been considered.
  • •Patients who, according daily clinical practice, have been treated with sunitinib between February 2012 to end of inclusion period, with a follow up of at least 6 months.
  • •Patients with a baseline imaging study (TC with arterial phase) and, at least, a 6-months follow-up evaluation. Patients with progression or exitus before the first imaging evaluation will not be included.

排除标准

  • •Patients with a follow-up of <6months because of any other cause beyond progression of disease or exitus.
  • •Patients without a baseline radiological evaluation or at 3/6 months.
  • •Patients who do not accept to participate in the study.
  • •Patients with anti-angiogenic treatment within 3 months prior to the start of sunitinib treatment.
  • •Patients treated with sunitinib plus any other anti-proliferative agent beyond ASS.

结局指标

主要结局

Response to treatment

时间窗: 3 months

According Choi and RECIST Criteria

次要结局

  • Progression Free Survival on partial response(3 months)
  • Impact of Response to Treatment and Progression Free Survival(3 months)
  • Impact of Choi criteria and Progression of Disease(3 months)
  • Impact of Tumor Uptake on Response to Treatment(3 months)
  • Progression Free Survival on Stable Disease(3 months)

研究者

发起方
Grupo Espanol de Tumores Neuroendocrinos
申办方类型
Other
责任方
Sponsor

研究点 (10)

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