The TIOB - Collection of Patients' Biospecimens for Analysis of Immunological and Molecular Biomarkers.

Sponsor
Baylor Research Institute (Other)
Overall Status
Recruiting
CT.gov ID
NCT05371756
Collaborator
Translational Genomics Research Institute (Other)
100,000
1
384
260.4

Study Details

Study Description

Brief Summary

The purpose of the Texas Immuno-Oncology Biorepository (TIOB) is to collect and store well-defined and well-annotated serial biospecimens of tissue, blood, urine and stool in a longitudinal manner from cancer patients who are receiving either standard of care surgical interventions and or FDA approved immunotherapeutics across the largest not-for-profit health system in Texas. Comprehensive clinical and radiological data from a diverse population of patients with different racial, social and ethnic backgrounds matched with serial biospecimens over a patients journey with cancer marks the TIOB as a unique research facility.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The goal of establishing the Texas Immuno-Oncology Biorepository (TIOB) is to create a research facility that purposely consents patients to collect, catalog, process, store, and analyze biospecimens with well-annotated clinical/radiological data from patients receiving surgical interventions or immunotherapeutics in our combined clinics throughout Texas. Potential types of studies that will be enabled by this resource will include but are not limited to (a) morphological studies including immunohistochemistry, (b) genomic and molecular analysis, including circulating, cell-free DNA, RNA, as well as extracellular vesicles and their cargo, (c) proteomic analysis involving protein isolation, (d) interrogation of circulating immune cells as well as the underlying tumor immune microenvironment, and (e) single-cell and spatial transcriptomics. Correlation of these studies with clinical, treatment outcome, and demographic information will be possible. Translation of multi-omics technologies will be a key feature of the TIOB and data integration strategies including genomics, epigenomics, transcriptomics, proteomics, radiomics, metabolomics and microbiomics will be possible and offer opportunities to improve our understanding of the complex biological interactions that define cancer.

    Study Design

    Study Type:
    Observational [Patient Registry]
    Anticipated Enrollment :
    100000 participants
    Observational Model:
    Case-Control
    Time Perspective:
    Prospective
    Official Title:
    The Texas Immuno-Oncology Biorepository: Collection of Patients' Biospecimens for Analysis of Immunological and Molecular Biomarkers That Predict Benefit/Resistance to Cancer Therapeutics.
    Actual Study Start Date :
    Sep 11, 2020
    Anticipated Primary Completion Date :
    Sep 11, 2050
    Anticipated Study Completion Date :
    Sep 11, 2052

    Outcome Measures

    Primary Outcome Measures

    1. Develop a biorepository [30 years]

      Develop a biorepository that ensures molecular integrity and clinical relevance of quality human biospecimens and aligned clinical data for development of new diagnostic and therapeutic technology.

    2. Release of specimens [30 years]

      Implement release of specimens from biorepository for testing.

    Secondary Outcome Measures

    1. Laboratory Testing [30 years]

      Immunohistochemistry

    2. Laboratory Testing [30 years]

      Genomic and Molecular analysis including circulating cell free DNA/RNA

    3. Laboratory Testing [30 years]

      Proteomic analysis

    4. Laboratory Testing [30 years]

      Single cell and Spatial transcriptomics

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Understand and willingness to sign written informed consent method.

    • Patients who are suspected by a physician of being at risk for developing cancer.

    • Patients with confirmed or clinically suspected malignancy by a physician. This includes but is not limited to candidates for immunotherapy, surgical candidates, patients receiving Standard of Care drugs, immunotherapy drugs, participating on a clinical trial with immunotherapy drugs, patients who have received immunotherapy drugs in the past, patients with any other approved or investigational disease management.

    Exclusion Criteria:
    • Patients unwilling to donate blood

    • Patients unwilling to provide informed consent for the collection of fresh or archived tumor tissue.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Baylor Scott & White Research Institute Dallas Texas United States 75246

    Sponsors and Collaborators

    • Baylor Research Institute
    • Translational Genomics Research Institute

    Investigators

    • Principal Investigator: Ronan Kelly, MD, Baylor Scott & White Research Institute

    Study Documents (Full-Text)

    More Information

    Publications

    None provided.
    Responsible Party:
    Baylor Research Institute
    ClinicalTrials.gov Identifier:
    NCT05371756
    Other Study ID Numbers:
    • 019-350
    First Posted:
    May 12, 2022
    Last Update Posted:
    May 12, 2022
    Last Verified:
    Apr 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Baylor Research Institute

    Study Results

    No Results Posted as of May 12, 2022