GBCPRT0008: Prospective Collection of Surplus Surgical Tumor Tissues and Pre-surgical Blood Samples

Sponsor
Global BioClinical (Industry)
Overall Status
Enrolling by invitation
CT.gov ID
NCT01792882
Collaborator
(none)
100
1
117.9
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Study Details

Study Description

Brief Summary

The study is intended to collect specimens to support the application of genome analysis technologies, including large-scale genome sequencing. This study will ultimately provide cancer researchers with specimens that they can use to develop comprehensive catalogs of genomic information on at least 50 types of human cancer. The study will create a resource available to the worldwide research community that could be used to identify and accelerate the development of new diagnostic and prognostic markers, new targets for pharmaceutical interventions, and new cancer prevention and treatment strategies. This study will be a competitive enrollment study conducted at multiple institutions.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    This study will enroll subjects diagnosed with various cancers and who are scheduled to undergo surgical treatment. Prior to scheduled surgery, subjects will be asked to donate a 10-20 ml blood sample. After surgery, surplus tissues (including tumor and adjacent normal tissues) not required for diagnosis will be collected. Subject clinical information will be collected, including basic demographic information, medical history, family history, current cancer history and treatment. After surgery, a final pathology report will be obtained for each subject's surgical specimen. In some instances and based on the cancer indications required, longitudinal data may also be collected at a frequency of every 6 months to once per year. Longitudinal data will include information on study subject survival and disease recurrence.

    Study Design

    Study Type:
    Observational
    Anticipated Enrollment :
    100 participants
    Observational Model:
    Other
    Time Perspective:
    Prospective
    Official Title:
    Prospective Collection of Surplus Surgical Tumor Tissues and Pre-surgical Blood Samples
    Study Start Date :
    Feb 1, 2013
    Anticipated Primary Completion Date :
    Dec 1, 2022
    Anticipated Study Completion Date :
    Dec 1, 2022

    Arms and Interventions

    Arm Intervention/Treatment
    Cancer Subjects

    Outcome Measures

    Primary Outcome Measures

    1. Tumor genetic sequence variation [up to 18 months]

      The specimens collected for this project will support genomic studies on the molecular basis of cancer. This study aims to collect specimens for a project that will systematically explore a spectrum of genomic changes involved in human cancer. Specifically the project will analyze DNA copy number changes, including large (on the order of chromosomal segments) and small (1,000 to 100,000 KB) scale rearrangements, transcription profiles, epigenetic modifications, sequence variation, and sequence in both tumor tissue and case-matched germline DNA. The suite of analysis platforms for collaborating laboratories will be applied to a common set of molecular analytes obtained from clinically annotated high-quality tumor specimens and case matched normal control specimens obtained form this specimen collection study. Initial measures critical to ensure specimen quality and qualification for subsequent analysis include confirmed histopathology and RNA integrity.

    Secondary Outcome Measures

    1. Transcription profile [up to 18 months]

    Other Outcome Measures

    1. Epigenetic modification [up to 18 months]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 90 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Any adult age

    • Any sex

    • Able to provide consent for surplus tissue and/or blood donation

    • Diagnosed with one of the cancer indications listed below:

    • Scheduled to undergo surgical resection of tumor (exception for hematological cancers)

    • Have not yet received treatment for cancer

    Exclusion Criteria:
    • Not diagnosed with required cancer indication

    • Not scheduled to undergo surgical resection of the tumor

    • Have already received cancer treatment (such as chemotherapy, radiation, surgery) for the current cancer or a previously diagnosed cancer

    • Not able to donate an adequate volume of blood to meet minimum requirements

    CANCER INDICATIONS:
    1. Bladder Cancer - Urothelial carcinoma - nonpapillary

    2. Bladder Cancer - Urothelial carcinoma - papillary

    3. Brain Cancer - Astrocytoma

    4. Brain Cancer - Glioblastoma

    5. Brain Cancer - Medulloblastoma

    6. Breast Cancer - Ductal Carcinoma

    7. Breast Cancer - Lobular Carcinoma

    8. Cervical Cancer - Squamous Cell Carcinoma

    9. Colorectal Cancer - Adenocarcinoma

    10. Esophageal Cancer - Adenocarcinoma

    11. Gastric Cancer

    12. Head and Neck Cancer - Squamous Cell Carcinoma

    13. Hematologic Cancer - Acute Lymphocytic Leukemia (ALL)

    14. Hematologic Cancer - Acute Myeloid Leukemia (AML)

    15. Hematologic Cancer - Chronic Lymphocytic Leukemia (CLL)

    16. Hematologic Cancer - Diffuse Large B-cell Lymphoma

    17. Hematologic Cancer - Multiple Myeloma (MM)

    18. Hematologic Cancer - Non-Hodgkins Lymphoma (NHL)

    19. Kidney Cancer - Papillary Carcinoma

    20. Kidney Cancer - Renal cell Carcinoma

    21. Liver Cancer - Hepatocellular Carcinoma

    22. Lung Cancer - Adenocarcinoma

    23. Lung Cancer - Squamous Cell Cancer

    24. Melanoma

    25. Pancreatic Cancer - Ductal Adenocarcinoma

    26. Prostate Cancer - Adenocarcinoma

    27. Sarcomas

    28. Thyroid Cancer - Follicular Carcinoma

    29. Thyroid Cancer - Papillary Carcinoma

    30. Uterine Cancer - Endometrial Carcinoma

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 GBC Seattle Washington United States 98104

    Sponsors and Collaborators

    • Global BioClinical

    Investigators

    • Study Director: Neil R Mucci, Global BioClinical

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Global BioClinical
    ClinicalTrials.gov Identifier:
    NCT01792882
    Other Study ID Numbers:
    • GBC PRT0008
    First Posted:
    Feb 15, 2013
    Last Update Posted:
    Mar 16, 2022
    Last Verified:
    Mar 1, 2022
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Mar 16, 2022