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
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
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