Status:

RECRUITING

Obtaining Solid Tumor Tissue From People Having Biopsy or Surgery for Certain Types of Cancer

Lead Sponsor:

National Cancer Institute (NCI)

Conditions:

Colorectal Neoplasms

Gastric Neoplasms

Eligibility:

All Genders

2+ years

Brief Summary

Background: \- Recent advances in cancer research have led to new therapies to treat the disease. It is important to continue these advances and discover new ones. To do that, researchers need tissue...

Detailed Description

Background: Recent advances and insights into the molecular pathogenesis of cancer have led to the development of novel molecular and biologic targeted therapies for the treatment of advanced cancer ...

Eligibility Criteria

Inclusion

  • INCLUSION CRITERIA:
  • Participants must be 2 years of age or older. Note: Participants greater than or equal to 2 and \< 18 years of age may only participate in research sample collection if the tissue acquisition is performed during a clinically indicated surgical procedure, and the biospecimen sampling (e.g., blood, urine, ascites, bile, or \[clinically indicated\] resected tumor tissue) does not add risk to the clinically indicated procedures.
  • Participants who have premalignant, primary, or metastatic solid tumors based upon either radiographic or clinical suspicion, biochemical testing, a genetic predisposition, or histological/cytological analysis that requires surgery or biopsy as part of the diagnosis, prevention, treatment, and/or follow-up.
  • Participants without solid tumors in whom a diagnostic, preventative, or therapeutic intervention is being performed, but for whom surgical quality and safety outcomes data are generated.
  • Participants should have laboratory and physical examination parameters within acceptable limits prior to biopsy or surgery.
  • Participants must be planning to undergo surgery or biopsy as part of their normal treatment plan.
  • Ability of participant, parent/guardian or legally authorized representative (LAR) to understand and the willingness to sign a written informed consent document.
  • EXCLUSION CRITERIA:
  • None.

Exclusion

    Key Trial Info

    Start Date :

    July 21 2013

    Trial Type :

    OBSERVATIONAL

    Allocation :

    ESTIMATED

    End Date :

    Estimated Enrollment :

    1800 Patients enrolled

    Trial Details

    Trial ID

    NCT01915225

    Start Date

    July 21 2013

    Last Update

    January 8 2026

    Active Locations (1)

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    Page 1 of 1 (1 locations)

    1

    National Institutes of Health Clinical Center

    Bethesda, Maryland, United States, 20892