Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 9:12 PM
Ignite Modification Date:
2025-12-24 @ 9:12 PM
NCT ID:
NCT03442504
Eligibility Criteria:
Inclusion Criteria:
1. Primary breast tumor (ductal or lobular) expressing immunohistochemistry of hormone receptors (RP + and / or RE +, with significance level ≥ 10%) but not overexpressing HER2,
2. Metastatic stage with at least one lesion identifiable on the conventional balance sheet other than a liver injury,
3. Patient progressing under a 1st line of hormone therapy,
4. Patient candidate for a new second-line hormonal treatment,
5. Postmenopausal patient,
6. Karnofsky ≥ 70 or ECOG 0-1
7. Life expectancy of at least 6 months
8. Creatinine \<= 2.5 normal
9. Social insured patient
10. Signed informed consent
Exclusion Criteria:
1. HER2 overexpressing primary tumor in immunohistochemistry,
2. Tumor that does not significantly (\<10%) express the hormonal receptors,
3. Hormonal treatment in progress,
4. Contraindication to a new second-line hormonal treatment,
5. Patient receiving or likely to receive second-line chemotherapy in the course of the evolution of her breast cancer,
6. Persons deprived of liberty or guardianship,
7. Impossibility of submitting to the medical examination of the test for geographical, social or psychological reasons,
8. Serious illness or comorbidity assessed at risk,
9. History of cancer within 5 years, with the exception of cutaneous carcinomas other than melanomas, or carcinoma in situ of the cervix,
10. Intellectual inability to sign informed consent.
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT03442504
Study Brief:
Protocol Section:
NCT03442504