Actively Recruiting
Developing Breast (Cancer) Organoids
Led by Maastricht Radiation Oncology · Updated on 2026-05-12
60
Participants Needed
1
Research Sites
295 weeks
Total Duration
On this page
Sponsors
M
Maastricht Radiation Oncology
Lead Sponsor
M
Maastricht University Medical Center
Collaborating Sponsor
AI-Summary
What this Trial Is About
Currently, only a few validated biomarkers and models exist guiding or predicting treatment response for specific patient groups. Therefore, a patient-tailored clinical model needs to be developed to address tumour heterogeneity and thereby guide treatment selection on an individualized level. Organoids are patient-derived aggregates that grow in 3D and maintain self- renewal pluripotency and lineage-specific differentiation. Therefore, in contrast with conventional cell lines, they are thought to sustain patient heterogeneity and characteristics and are consequently already in use for drug response screening. This now offers the opportunity to investigate if the primary patient breast cancer organoid platform reflects disease progression, treatment response and relapse in patients with different clinical breast cancer subtypes. Goal: To develop a living biobank from prospective patient-derived breast cancer tissue. The questions we will address are: 1. Do patient-derived breast cancer organoids retain the clinical behaviour and characteristics of the primary patient tumour? 2. Can BC organoids be used to derive prognostic and predictive biomarkers to inform treatment decisions? 3. Can the investigators utilize BC organoids to discover novel actionable targets and combination treatments for therapeutic intervention for breast cancer patients? 4. Can BC organoids be used to discover mechanisms of treatment resistance and relapse?
CONDITIONS
Official Title
Developing Breast (Cancer) Organoids
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Female
- Older than 18 years
- Family history of breast cancer
- Breast cancer confirmed by tissue testing with subtypes: ER-, PR-, HER2-; ER+, PR+, HER2-; ER+, PR+, HER2+
- Scheduled for primary breast surgery (lumpectomy or mastectomy)
You will not qualify if you...
- Physically or mentally unable or incompetent to provide informed consent
AI-Screening
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Trial Site Locations
Total: 1 location
1
Maastricht University Medical Center
Maastricht, Netherlands, 6202 AZ
Actively Recruiting
Research Team
C
Chantal Overhof
CONTACT
A
Ann Claessens
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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