Study of Tumor Tissue Samples From Patients Who Have Undergone Surgery for Advanced Stage III or Stage IV Ovarian Epithelial Cancer

Sponsor
Gynecologic Oncology Group (Other)
Overall Status
Recruiting
CT.gov ID
NCT01000259
Collaborator
National Cancer Institute (NCI) (NIH)
174
1

Study Details

Study Description

Brief Summary

This research study is looking at tumor tissue samples from patients who have undergone surgery for advanced stage III or stage IV ovarian epithelial cancer. Studying samples of tumor tissue from patients with cancer in the laboratory may help doctors learn how tumor infiltrating T cells can predict how patients will respond to treatment.

Condition or Disease Intervention/Treatment Phase
  • Other: Laboratory Biomarker Analysis

Detailed Description

PRIMARY OBJECTIVES:
  1. To validate the ability of intratumoral tumor-infiltrating T lymphocytes (TILs) to predict progression-free survival (PFS) in patients with suboptimally debulked advanced stage III or IV ovarian epithelial cancer.

  2. To validate the ability of intratumoral TILs to predict PFS in patients with optimally debulked disease.

SECONDARY OBJECTIVES:
  1. To validate the ability of intratumoral TILs to predict overall survival of patients with suboptimally debulked disease.

  2. To validate the ability of intratumoral TILs to predict overall survival of patients with optimally debulked disease.

OUTLINE:

Patients are stratified according to status of debulked disease (suboptimal vs optimal).

Previously collected tumor tissue samples are analyzed for tumor-infiltrating lymphocytes (TIL) via immunohistochemistry and double immunofluorescence assays using standard immunostaining.

Study Design

Study Type:
Observational
Anticipated Enrollment :
174 participants
Official Title:
Validation of Tumor-Infiltrating T-Cells as a Biomarker for Advanced Epithelial Ovarian Cancer
Study Start Date :
Sep 1, 2004
Anticipated Primary Completion Date :
Jan 1, 2100

Arms and Interventions

Arm Intervention/Treatment
Ancillary-Correlative

Previously collected tumor tissue samples are analyzed for TIL via immunohistochemistry and double immunofluorescence assays using standard immunostaining.

Other: Laboratory Biomarker Analysis
Samples are analyzed in laboratory studies

Outcome Measures

Primary Outcome Measures

  1. Overall survival curves [Baseline]

    The Kaplan-Meier method will be used to estimate the survival curves, and the log-rank test will be used to test the difference between survival curves for TIL positive and negative patients. All of the tests will be two-sided and the significant levels will be set a 0.05.

  2. Progression-free survival curves [Baseline]

    The Kaplan-Meier method will be used to estimate the survival curves, and the log-rank test will be used to test the difference between survival curves for TIL positive and negative patients. All of the tests will be two-sided and the significant levels will be set a 0.05.

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Diagnosis of stage III or IV ovarian epithelial cancer and enrolled on Gynecologic Oncology Group (GOG)-0136 and a GOG front-line platinum/taxol chemotherapy trial (GOG-0114, GOG-132, GOG-0158, or GOG-0162)

  • Must have fixed and paraffin-embedded tissue from primary surgery available from 1 of the following sources:

  • Patients enrolled on GOG-0136 and a GOG front-line platinum/taxol chemotherapy trial(GOG-0114, GOG-0132, GOG-0158, and GOG-0162)

  • Patients who have had either optimal or suboptimal cytoreductive surgery

  • Patients for whom adequate demographic data, including major prognostic factors and follow-up information, were collected

  • Evaluable patients must have had measurable or nonmeasurable disease

  • Demographic and follow-up data available

Contacts and Locations

Locations

Site City State Country Postal Code
1 Gynecologic Oncology Group Philadelphia Pennsylvania United States 19103

Sponsors and Collaborators

  • Gynecologic Oncology Group
  • National Cancer Institute (NCI)

Investigators

  • Principal Investigator: George Coukos, Gynecologic Oncology Group

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Gynecologic Oncology Group
ClinicalTrials.gov Identifier:
NCT01000259
Other Study ID Numbers:
  • GOG-8005
  • NCI-2011-02279
  • GOG-8005
  • CDR0000391277
  • GOG-8005
  • GOG-8005
  • U10CA027469
First Posted:
Oct 23, 2009
Last Update Posted:
May 5, 2017
Last Verified:
May 1, 2017
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 5, 2017