UPTIDER is a prospective, interventional, non-Investigational Medicinal Product (non-IMP), non-commercial, single centre post-mortem tissue donation program for metastatic breast cancer patients or patients with a germline pathogenic variant with a moderate to high lifetime risk of breast cancer and at least one malignancy at time of death. The overarching objective of UPTIDER is (i) to unravel metastatic breast cancer evolution, biology, heterogeneity and treatment resistance and (ii) to assess pathogenicity and tumour biology in hereditary cancer syndromes with a high lifetime risk of breast cancer; both through extensive post-mortem multi-level and multi-region sample analysis.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
BASIC_SCIENCE
Masking
NONE
Enrollment
100
Blood draw at inclusion
Sample collection (both liquids, tumour tissue and non-tumour tissue) during post-mortem research autopsy
UZ Leuven
Leuven, Belgium
RECRUITINGPercentage of patients consenting to participate in the pilot phase
Should be equal to or above 50%
Time frame: Baseline
Median time elapsed between moment of death and start of the autopsy
Should be equal to or less than 12h
Time frame: During autopsy
Median time elapsed between collection of first and last sample
Should be equal to or less than 8h
Time frame: During autopsy
Percentage of metastatic organs sampled
Should be equal to or more than 75%
Time frame: During autopsy
Percentage of samples with sufficient quality of DNA extracted
A260/A280 ratio
Time frame: During autopsy
Percentage of samples with sufficient quality of RNA extracted
RNA integrity number (RIN)
Time frame: During autopsy
Concordance between TILs and clinical response to treatment
Standard histopathological review
Time frame: During autopsy
Rate of T cell exhaustion
RNA sequencing
Time frame: During autopsy
Number of mutations in each tumor lesion
Whole exome sequencing
Time frame: During autopsy
Type of mutations in each tumor lesion
Whole exome sequencing
Time frame: During autopsy
Percentage of Tumour Infiltrating Lymphocytes (TILs)
Standard histopathological review
Time frame: During autopsy
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.