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NCT Number: NCT04531696

UZ/KU Leuven Program for Post-mortem Tissue Donation to Enhance Research

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.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age ≥ 18 years.
  • Signature of informed consent by the subject.
  • Metastatic breast cancer, or hereditary cancer syndrome with a moderate to high lifetime risk of breast cancer, for which the patient is treated/followed in UZ Leuven or treated in another hospital and referred to UZ Leuven specifically for the trial.

Additional inclusion criteria for the different substudies:

  • Pilot phase: no additional inclusion criteria.
  • ILC substudy: histologically confirmed history of ILC.
  • IBC substudy: history of IBC, fulfilling the following criteria described by Dawood et al: rapid onset of breast erythema, oedema and/or peau d'orange and/or warm breast with or without an underlying palpable mass, duration of history of no more than 6 months, erythema occupying at least one-third of the breast and pathological confirmation of invasive carcinoma.
  • Hereditary cancer syndrome substudy: confirmed presence of a germline mutation known to be associated with a moderate to high lifetime risk of BC (e.g. known pathogenic variants in the genes BRCA1/2, CHEK2, TP53, PALB2) and presence of at least one malignant lesion at time of inclusion (of any origin) .
  • Other substudies: no additional inclusion criteria.

Exclusion criteria

  • Presence of a transmissible disease that can form a risk to the health of researchers or others handling the body or patient samples. This includes but is not limited to the following infectious diseases: human immunodeficiency virus (HIV), active hepatitis C virus (HCV), encephalitis of unknown cause, Creutzfeldt-Jakob disease, rabies, active malaria, active tuberculosis, active SARS-CoV-2 infection.
  • Presence of any factors that could logistically or organizationally impede the study or the performance of sampling within a reasonable post-mortem time frame. This includes but is not limited to: residence of the subject at a faraway distance from the UZ Leuven hospital; residence of the subject on territory outside of Belgium; impossibility to notify the clinician confirming the death and the researchers within a reasonable time frame in case of death.

Additional exclusion criteria for the different substudies:

  • ILC substudy, IBC substudy: diagnosis of a malignancy other than breast cancer in the 5 years prior to inclusion. Exceptions include basal cell carcinoma of the skin or squamous cell carcinoma of the skin and in situ cervical carcinoma.

Treatment and study plan

Blood draw

Procedure

Blood draw at inclusion

Post-mortem tissue collection

Procedure

Sample collection (both liquids, tumour tissue and non-tumour tissue) during post-mortem research autopsy

Primary outcomes

  1. Percentage of patients consenting to participate in the pilot phase

    Time frame: Baseline

    Should be equal to or above 50%

  2. Median time elapsed between moment of death and start of the autopsy

    Time frame: During autopsy

    Should be equal to or less than 12h

  3. Median time elapsed between collection of first and last sample

    Time frame: During autopsy

    Should be equal to or less than 8h

  4. Percentage of metastatic organs sampled

    Time frame: During autopsy

    Should be equal to or more than 75%

  5. Percentage of samples with sufficient quality of DNA extracted

    Time frame: During autopsy

    A260/A280 ratio

  6. Percentage of samples with sufficient quality of RNA extracted

    Time frame: During autopsy

    RNA integrity number (RIN)

Secondary outcomes

  1. Concordance between TILs and clinical response to treatment

    Time frame: During autopsy

    Standard histopathological review

  2. Rate of T cell exhaustion

    Time frame: During autopsy

    RNA sequencing

  3. Number of mutations in each tumor lesion

    Time frame: During autopsy

    Whole exome sequencing

  4. Type of mutations in each tumor lesion

    Time frame: During autopsy

    Whole exome sequencing

  5. Percentage of Tumour Infiltrating Lymphocytes (TILs)

    Time frame: During autopsy

    Standard histopathological review

Study contacts

Contact information is provided by the study sponsor or research team.

Christine Desmedt, PhD

CONTACT

[email protected]

003216193306 ext. www.ltbcr.be

Giuseppe Floris, MD PhD

CONTACT

[email protected]

003216336539

Sponsors and collaborators

Lead sponsor

Universitaire Ziekenhuizen KU Leuven

Other

Collaborators

  • KU Leuven
  • Universiteit Antwerpen

Registry information

Acronym: UPTIDER

Important dates

Study start
2020
Primary completion
2035
Study completion
2035
First posted
Aug 28, 2020
Registry last updated
Jun 28, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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