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A Limited Institution Study of the Local and Systemic Effects of Intraperitoneal Chemotherapy in the Treatment of Previously-Untreated, Invasive Epithelial Ovarian, Fallopian Tube and Primary Peritoneal Carcinoma

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City:   Springfield
State:   Illinois
Zip Code:   62781
Conditions:   Fallopian Tube Cancer - Ovarian Cancer - Primary Peritoneal Cavity Cancer
Purpose:   RATIONALE: Studying samples of tumor tissue, peritoneal cavity fluid, and blood from patients receiving intraperitoneal chemotherapy may help doctors learn more about the effects of intraperitoneal chemotherapy on cells. It may also help doctors identify and learn more about biomarkers related to cancer. PURPOSE: This research study is studying biomarkers in patients with previously untreated invasive ovarian epithelial, fallopian tube, or peritoneal cancer.
Study Summary:   OBJECTIVES: - Determine the feasibility of obtaining peritoneal fluid, peritoneal washings, and peripheral blood in patients receiving intraperitoneal (IP) chemotherapy for ovarian cancer at multiple institutions. - Assess the recovery and viability of peripheral blood mononuclear cells and immune cell subsets in peritoneal fluid and washings. - Assess the amount of peritoneal fluid that can be obtained pre-treatment and at specified time points during the course of IP chemotherapy. - Quantify the type and number of cells in peritoneal fluid, peritoneal washings, and blood recovered from women before and during treatment with platinum- and taxane-based IP chemotherapy. - Determine the levels of immunomodulatory cytokines in peritoneal fluid, peritoneal washings, and blood recovered from women before and during treatment with platinum- and taxane-based IP chemotherapy. - Generate exploratory information on the impact of platinum- and taxane-based IP chemotherapy on immunomodulatory cytokines and tumor-associated alterations in cell phenotypes of peritoneal fluid, peritoneal washings, and blood. - Determine the feasibility of obtaining peritoneal fluid, peritoneal washings, and peripheral blood in patients receiving intravenous (IV) chemotherapy for ovarian cancer at multiple institutions (limited to patients that receive an IP catheter at the time of surgery and the catheter is left in by the investigator, but are subsequently treated with IV chemotherapy). - Assess the amount of peritoneal fluid that can be obtained pre-treatment and at specified time points during the course of IV chemotherapy. - Assess the recovery and viability of peripheral blood mononuclear cells and immune cell subsets in peritoneal fluid and washings. - Quantify the type and number of immune cells in peritoneal fluid, peritoneal washings, and blood recovered from women before and during treatment with platinum- and taxane-based IV chemotherapy. - Determine levels of immunomodulatory cytokines in peritoneal fluid, peritoneal washings, and blood recovered from women before and during treatment with platinum- and taxane-based IV chemotherapy. - Generate exploratory information on the impact of platinum- and taxane-based IV chemotherapy on immunomodulatory cytokines tumor-associated alterations in cell phenotypes of peritoneal fluid, peritoneal washings, and blood. - Explore whether there is a relationship between immune cell populations measured in peripheral blood, peritoneal fluid, and peritoneal washings AND immune cell subsets measured by immunohistochemistry in archival formalin-fixed, paraffin-embedded tumor tissue. OUTLINE: This is a multicenter study. Patients are assigned to a group based on which arm of treatment they are randomized to receive on GOG-0252. - Group A (IP catheter removed): Archival formalin-fixed, paraffin-embedded tumor (collected during previous surgery), peritoneal fluid, peritoneal wash, and blood (for cell, plasma, and serum isolation) samples are collected before course one and blood (for cell, plasma, and serum isolations) is collected before courses two and three for translational research. - Group B (IP catheter in place): Archival formalin-fixed, paraffin-embedded tumor (collected during previous surgery), peritoneal fluid, peritoneal wash, and blood (for cell, plasma, and serum isolation) samples are collected before course one and peritoneal fluid, peritoneal wash, and blood (for cell, plasma, and serum isolations) before courses two and three for translational research.
Criteria:   DISEASE CHARACTERISTICS: - Diagnosis of epithelial ovarian, fallopian tube, or peritoneal cancer - Newly diagnosed disease - Chemotherapy naïve - Patients must be enrolled on GOG-0252 - Patients must have an IP catheter placed prior to initiating platinum- and taxane-based chemotherapy on GOG-0252 - Patients must have signed an approved informed consent for specimen collection and participation in this translational research study PATIENT CHARACTERISTICS: - Not specified PRIOR CONCURRENT THERAPY: - See Disease Characteristics
NCT ID:   NCT01295489
Primary Contact:   Principal Investigator
Robert P. Edwards, MD
University of Pittsburgh

Backup Contact:   N/A
Location Contact:   Springfield, Illinois 62781
United States

Clinical Trials Office - Regional Cancer Center at Memorial Me
Phone: 217-788-4233

Site Status: Recruiting

Data Source:   ClinicalTrials.gov
Date Processed:   May 25, 2013
Modifications to this listing:   Only selected fields are shown, please use the link below to view all information about this clinical trial.
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