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

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
AgeNot listed
SponsorGynecologic Oncology Group

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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)

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

Disqualifiers

None

Trial design

Treatments tested in this trial

  • Laboratory Biomarker Analysis

    Other intervention

    Samples are analyzed in laboratory studies

Treatment groups

174 Participants
are divided into 1 treatment group
Group A: Ancillary-Correlative1 intervention

Trial outcomes

Primary outcomes

1

Overall survival curves

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.

Time frame
Baseline
2

Progression-free survival curves

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.

Time frame
Baseline

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Gynecologic Oncology Group

Lead sponsor

National Cancer Institute (NCI)

Collaborator