Clinical, Histological and In-depth Molecular Characterization as Well as Experimental Models of Liver Metastasis From Patients With Breast Cancer in Order to Identify New Potential Treatment Avenues.

NCT ID: NCT05720676

Last Updated: 2023-02-09

Basic Information

• Recruitment Status: UNKNOWN
• Total Enrollment: 20 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2023-03-31
• Study Completion Date: 2025-03-31

Brief Summary

The goal of this observational study is to learn about breast cancer liver metastasis in patients who met the following criteria:

• female;
• be ≥ 18 years of age on the day of signing informed consent;
• confirmed diagnosis of breast cancer liver metastases. Newly diagnosed patients with de-novo liver metastases are eligible;
• be planned for liver surgery.

The main questions it aims to answer are:

1. To characterize the tumour cells and their microenvironment in the liver metastases at the transcriptomic and protein single-cell level;

2. To determine the levels and patterns of immune infiltrates in liver metastases from BC patients;

3. To identify biological features associated with the histopathological growth patterns in liver metastases.

4. To create patient-derived xenografts (PDX) and organoids (PDO) from liver metastases isolated from patients with BC;

5. To perform a histopathological and molecular comparison of liver metastases, PDX and PDO isolated from the same patient

Participants will be willing and able to provide written informed consent for this study and tissue samples for research purposes.

Conditions

Breast Cancer; Liver Metastases

Study Design

• Observational Model Type: CASE_ONLY
• Study Time Perspective: PROSPECTIVE

Eligibility Criteria

Inclusion Criteria

• be willing and able to provide written informed consent for this study;
• female;
• be ≥ 18 years of age on the day of signing informed consent;
• confirmed diagnosis of breast cancer liver metastases. Newly diagnosed patients with de-novo liver metastases are eligible;
• be planned for liver surgery;
• be willing to provide tissue samples for research purposes.

Exclusion Criteria

• unwillingness to provide the samples or clinical information needed for the study;
• History of radiofrequency destruction (RF), stereotactic Body Radiotherapy (SBRT) or intra-arterial treatment such as chemoembolization (TACE) or selective internal radiation therapy (SIRT) performed on the metastasis to be examined (accepted if performed in other metastasis);
• Has an active autoimmune disease that has required systemic treatment in the past 2 years prior to the surgery (i.e. with use of disease modifying agents, corticosteroids or immunosuppressive drugs). Replacement therapy (e.g., thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a form of systemic treatment;
• Presence of immunodeficiency or immune dysregulatory diseases and conditions which require active immune modulatory treatment of any kind, or required treatment in the past two years from date of diagnosis of breast cancer;
• History or current evidence of any condition, therapy, or laboratory abnormality that might confound the results in the opinion of the treating investigator.

• Minimum Eligible Age: 18 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: No

Sponsors

Jules Bordet Institute

OTHER

Sponsor Role: collaborator

Erasme University Hospital

OTHER

Sponsor Role: collaborator

GZA Ziekenhuizen Campus Sint-Augustinus

OTHER

Sponsor Role: collaborator

KU Leuven

OTHER

Sponsor Role: lead

Responsible Party

Sophia Leduc

PhD Student

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Sophia Leduc

Leuven, , Belgium

Countries

Belgium

Facility Contacts

Sophia Leduc, PhD

Role: primary

Other Identifiers

S-64813

Identifier Type: -

Identifier Source: org_study_id