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This study investigates the role of intrinsic molecular subtypes in predicting prognosis and treatment response in breast cancer patients who carry a BRCA1 or BRCA2 gene variant. Patients aged 18 and over who carry a pathogenic germline variant in BRCA1 or BRCA2 and have HR+/HER2-negative breast cancer may take part. This is a study with no assigned phase and it is currently recruiting participants.
The summary above is a plain-language rendering of the official record. The original English title is shown for reference.
Criteria are reproduced from the ClinicalTrials.gov record in the original English. Only the trial team can determine eligibility.
Inclusion Criteria: * Age 18 years or older * Patients carrying a pathogenic or likely pathogenic germline variant in BRCA1 or BRCA2 with a histologically confirmed diagnosis of HR+/HER2-negative breast cancer * Patients with available hospital and/or outpatient medical records for clinical data collection * Presence of available formally fixed paraffin-embedded (FFPE) breast tumor tissue (primary or metastatic site) Exclusion Criteria: * None