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临床试验/NCT01956513
NCT01956513撤回不适用

Etude ADC Apport de l'IRM Dans l'évaluation du Coefficient de Diffusion Apparent et prédiction de la réponse à la chimiothérapie néoadjuvante Dans le Cancer du Sein

Centre Jean Perrin0 个研究点开始时间: 2012年3月1日最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
发起方
主要终点
Variation of apparent diffusion coefficient before / after a cycle of neoadjuvant chemotherapy or before / after modification of the treatment sequence and correlated with histologic response

研究概览

简要总结

The main objective of the study is to assess the sensitivity and the specificity of the variation of apparent diffusion coefficient for prediction, after a course of neoadjuvant chemotherapy or after modification of the treatment sequence, the pathological response at the end of chemotherapy

研究设计

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

入排标准

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

入选标准

  • Age> 18 years.
  • Patient suffering from a breast tumor, regardless of the stage and size
  • Patient requiring neoadjuvant chemotherapy
  • Patient has the ability to undergo 18F-FDG-PET at baseline, at end of cycle 1 and at the end of neoadjuvant treatment before surgery
  • Compulsory affiliation to a social security system.
  • Obtaining informed consent in writing, signed and dated.

排除标准

  • Patient with cognitive or psychiatric disorders.
  • Patient deprived of liberty by a court or administrative.
  • Patient with signs against the achievement of MRI, mammography and ultrasound
  • Patient metastatic
  • Patient with prior chemotherapy, radiotherapy and hormone therapy for her breast cancer
  • Pregnant women, current lactation
  • Patient suffering from uncontrolled diabetes (> 11 mmol / L)

结局指标

主要结局

Variation of apparent diffusion coefficient before / after a cycle of neoadjuvant chemotherapy or before / after modification of the treatment sequence and correlated with histologic response

时间窗: One year

次要结局

未报告次要终点

研究者

发起方
Centre Jean Perrin
申办方类型
Other
责任方
Sponsor

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