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临床试验/EUCTR2021-003601-21-FR
EUCTR2021-003601-21-FR进行中(未招募)1 期

Impact of 18F-FES TEP on therapeutical management in patients with metastatic breast cancer, ER positive and HER2 negative, in relapse after a first line of treatment combining hormonal therapy - ESTROTIMP

Zionexa0 个研究点目标入组 152 人开始时间: 2021年7月19日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
Zionexa
入组人数
152

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
Female

入选标准

  • 1. Woman aged at least 18 years old on inclusion
  • 2. Primary breast cancer expressing hormonal estrogen receptors in IHC (ER = 10%)
  • 3. Primary breast tumor HER2 negative (0, 1+, 2+ FISH negative)
  • 4. Metastatic stage with at least one lesion identifiable on the conventional work-up other than a hepatic lesion
  • 5. Patient in a situation of recurrence of the first line of treatment combining a CDK4 / 6 inhibitor and a hormone therapy
  • 6.Patient having performed a PET / CT with FDG during the follow-up of the first metastatic line defining the relapse or accepting to perform a PET / CT with the baseline FDG for the extension assessment (according to the recommendations of the GBU of the examinations of 'medical imaging). A period of 2 to 28 days will be respected between the 2 PET / CT (FDG / FES).
  • 7.ECOG 0, 1 or 2
  • 8. Life expectancy of at least 12 months
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 52
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 100

排除标准

  • 1. Isolated hepatic metastases (taking into account the high physiological hepatic uptake of FES)
  • 2. Patients in the first metastatic line or beyond the second metastatic line
  • 3. Person with a known allergy to any of the components of EstroTep
  • 4. Patients who have been treated with a CDK4 / 6 inhibitor in combination with a first-line metastatic SERM or SERD
  • 5. Woman of childbearing potential without effective contraception
  • 6. Serious intercurrent illness or co-morbidity assessed as risk

研究者

发起方
Zionexa

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