No registrations found.
ID
Source
Brief title
Health condition
Breast Cancer
Sponsors and support
Intervention
Outcome measures
Primary outcome
To develop a patient derived clinical model of breast (cancer) organoids using tissue biopsies.
Secondary outcome
Histological, genomic, and proteomic analysis will be conducted to provide insight in whether these organoids are patient representative and could result in patient tailored treatment. Furthermore, existing and newly developed therapies will be tested on this model - with the ultimate goal, to predict therapy response and/or resistance. Therapy efficacy will be assessed using viability assays, and genomic- and proteomic analysis.
Background summary
Background: Breast cancer is the second most common diagnosed malignancy worldwide. Unfortunately, treatment efficacy cannot be guaranteed and is highly influenced by tumor heterogeneity. To combat this, a patient tailored clinical model needs to be developed to guide the patient’s treatment regimen.
Herein, the development in the field of (tumor) organoids provides new opportunities. Organoids are patient derived aggregates which grow in 3D and maintain self-renewal pluripotency and lineage specific differentiation. Therefore, in contrast with conventional cell lines, they are thought to maintain patient heterogeneity and characteristics. However, a clear understanding and developed protocol for breast (cancer) organoids test multiple therapy options and guide therapy is lacking.
Hypothesis: We hypothesize that breast cancer organoids will result in a prospective clinical model that is predictive of treatment response.
Opportunity: The establishment and characterization of breast cancer organoids will yield conclusive information on the (epi)-genetic and phenotypic stability of organoids in culture, and the relevance of such organoids as patient avatars.
Impact: Breast cancer organoids may be used to prospectively predict response and guide the selection of more effective treatments improving and prolonging patient survival.
Study objective
We hypothesize that breast cancer organoids will result in a prospective clinical model that is predictive of treatment response.
Study design
n.a.
Intervention
Patients will undergo standard diagnostics and work-up according to the Dutch National Guidelines, including the marker placement procedure. During the marker placement procedure an accessory tumor tissue biopsy (14G needle) will be taken by an expert breast radiologist.
M.L. Smidt
Maastricht University Medical Center +
Department of Surgery
Maastricht 6202AZ
The Netherlands
+31 (0)433-877477
m.smidt@mumc.nl
M.L. Smidt
Maastricht University Medical Center +
Department of Surgery
Maastricht 6202AZ
The Netherlands
+31 (0)433-877477
m.smidt@mumc.nl
Inclusion criteria
- Female,
- >18 years,
- Breast cancer (proven by histopathology),
- Undergoing the marker placement procedure.
Exclusion criteria
- Physically or mentally incapable or incompetent to sign informed consent.
Design
Recruitment
Followed up by the following (possibly more current) registration
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Other (possibly less up-to-date) registrations in this register
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In other registers
Register | ID |
---|---|
NTR-new | NL7088 |
NTR-old | NTR7286 |
Other | ABR number : 65960 |