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Preservation of Fertility by Ovarian Stimulation Associated With Tamoxifen, Prior Chemotherapy for Breast Cancer (PRESAGE)

Phase 1
Conditions
Breast cancer
MedDRA version: 20.0Level: PTClassification code: 10006187Term: Breast cancer Class: 100000004864
Therapeutic area: Diseases [C] - Neoplasms [C04]
Registration Number
CTIS2024-516282-37-00
Lead Sponsor
Institut De Cancerologie De L Ouest
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Recruiting
Sex
Not specified
Target Recruitment
100
Inclusion Criteria

1.Obtaining signed informed consent prior to any trial-specific procedure, 10.Social protection, 2.Between 18 and 40 yo, 3.Histologically proven invasive breast carcinoma, 4.Indication for adjuvant or neoadjuvant chemotherapy validated by pre-therapy PCR, 5.T0-T1-T2-T3, 6.N0-N1-N2a, 7.M0 after extension assessment according to French INCa recommendations, 8.AMH (anti-müllerian hormone) =1 ng/mL and/or AFC (antral follicle count) = 5 (on ultrasound: ovaries puncturable transvaginally),, 9.HIV serology negative

Exclusion Criteria

1.Previous breast cancer, 2.History of any other cancer in the last 5 years, with the exception of basal cell and squamous cell skin cancers, 3.Pregnancy in progress, 4.Pulmonary embolism less than 6 months old, 5.Deep vein thrombosis less than 6 months old, 6.Dementia or altered mental state, 7.Legal incapacity or limited legal capacity. Medical or psychological conditions preventing the subject from understanding the study and signing the consent form (art. L.1121-6, L.1211-8, L.1211-9).

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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