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Interrogation of Exosome-mediated Intercellular Signaling in Patients With Pancreatic Cancer


2015-03


2027-03


2027-03


181

Study Overview

Interrogation of Exosome-mediated Intercellular Signaling in Patients With Pancreatic Cancer

The purpose of this study is to isolate and analyze exosomes, which are tiny carriers of important proteins and nucleic acids that serve as messenger systems in the blood and tissue. Blood and tissue from patients with pancreatic cancer will be compared with blood and tissue from patients with noncancerous pancreatic disease. Including patients without cancer will allow the investigators to establish "normal" values, which currently do not exist. The investigators will then look to see whether exosome activity has a connection to disease recurrence and outcomes in patients. The results of this study will be the basis for future studies exploring this area.

N/A

  • Pancreatic Cancer
  • Benign Pancreatic Disease
    • 15-015

    Study Record Dates

    These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

    Study Registration Dates Results Reporting Dates Study Record Updates

    2015-03-06  

    N/A  

    2025-02-05  

    2015-03-13  

    N/A  

    2025-02-10  

    2015-03-19  

    N/A  

    2025-02  

    Study Plan

    This section provides details of the study plan, including how the study is designed and what the study is measuring.

    Design Details

    Primary Purpose:
    N/A


    Allocation:
    N/A


    Interventional Model:
    N/A


    Masking:
    N/A


    Arms and Interventions

    Participant Group/ArmIntervention/Treatment
    Primary Outcome MeasuresMeasure DescriptionTime Frame
    successful isolation of exosomesisolation of at least 100,000 microvesicles is needed for exosomes purification for down stream applications such as proteomics and RNA sequencing.1 year
    Secondary Outcome MeasuresMeasure DescriptionTime Frame
    evaluation of the liver microenvironmentfor alterations in cellular infiltrate and ECM using IF and IHC1 year

    Contacts and Locations

    This section provides the contact details for those conducting the study, and information on where this study is being conducted.

    Study Contact

    Name: William Jarnagin, MD

    Phone Number: 212-639-7601

    Email:

    Study Contact Backup

    Name: Peter Kingham, MD

    Phone Number: 212-639-5260

    Email:

    Participation Criteria

    Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person’s general health condition or prior treatments.

    Ages Eligible for Study:
    ALL

    Sexes Eligible for Study:
    18 Years

    Accepts Healthy Volunteers:
    1

      Inclusion Criteria:

    • All patients ≥ 18 years of age undergoing pancreaticoduodenectomy, partial or complete pancreatectomy, and duodenal ampullectomy for presumed ductal adenocarcinoma, intraductal papillary mucinous neoplasm (IPMN) or pancreatic neuroendocrine tumors, without an invasive component; or other benign pancreatic disease will be eligible.
    • For third part of the study, recipient of neoadjuvant chemotherapy will be accrued to the neoadjuvant group (25 patients). Patients without neoadjuvant chemotherapy will be accrued to the non-neoadjuvant group (25 patients).

    • Exclusion Criteria:

    • The presence of metastatic disease or disease that precludes resection
    • For first and second part of the study, receipt of neoadjuvant chemotherapy or radiation for the index cancer within 6 months of being enrolled in the study
    • For third part of the study, receipt of neoadjuvant radiation for the index cancer within 6 months of being enrolled in the study
    • INR >2
    • Known clotting factor deficiency or hypercoagulable state
    • Any patient with the need or anticipated need for full anti-coagulation during hospitalization for the resection.
    • Receipt of antiplatelet agents (other than aspirin) in the preceding week prior to resection.
    • IPMN or pancreatic neuroendocrine tumors by radiographic imaging with high suspicion for invasive component Additionally, if at the discretion of the operating surgeon, blood collection would lead to undue morbidity, the patient will be excluded and replaced

    Collaborators and Investigators

    This is where you will find people and organizations involved with this study.

    • Weill Medical College of Cornell University
    • National Institutes of Health (NIH)
    • University of Pittsburgh

    • PRINCIPAL_INVESTIGATOR: William Jarnagin, MD, Memorial Sloan Kettering Cancer Center

    Publications

    The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

    General Publications

    No publications available