European Institute of oncology
Milan, Italy, 20141
Location status: Recruiting
Location contact
Elena Guerini Rocco, MD
CONTACT
Nicola Fusco, MD
CONTACT
NCT Number: NCT06762483
Development and validation of an integrated testing strategy for simultaneous detection of ESR-1 and gBRCA mutations via liquid biopsy in HR+/HER2- metastatic breast cancer (mBC) patients, and the creation of a digital gene library to support an evidence-based diagnostic algorithm
Interested in participating?
Request Info18 year and older
Female
Observational
Milan, Italy, 20141
Location status: Recruiting
Elena Guerini Rocco, MD
CONTACT
Nicola Fusco, MD
CONTACT
Breast cancer is the most prevalent type of tumor and the primary cause of cancer-related deaths among women globally (1). Approximately two-thirds of these tumors express hormone receptors (HR) and lack HER2 overexpression and/or amplification (2). Throughout treatment, resistance frequently develops, with underlying mechanisms that remain largely undefined (3).
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: 2 years
Optimize the patient journey for individuals with metastatic breast cancer (mBC) by enhancing the care pathway and promoting access to testing for ESR1 and gBRCA mutations.
Contact information is provided by the study sponsor or research team.
Nicola Fusco, MD
CONTACT
francesca lombardi, biologist
CONTACT
European Institute of Oncology
Other
Development and Validation of an Integrated Testing Strategy for Simultaneous Detection of ESR-1 and gBRCA Mutations Via Liquid Biopsy in HR+/HER2- Metastatic Breast Cancer (mBC) Patients, and the Creation of a Digital Gene Library to Support an Evidence-based Diagnostic Algorithm
Acronym: L2-268
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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