Collecting Tumor Samples From Patients With Gynecological Tumors

NCT00897442 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 275

Last updated 2016-10-28

No results posted yet for this study

Summary

This laboratory study is collecting tumor tissue and blood samples from patients with gynecologic tumors. Collecting and storing samples of tumor tissue and blood from patients with cancer to study in the laboratory may help in the study of cancer.

Conditions

  • Borderline Ovarian Clear Cell Tumor
  • Borderline Ovarian Serous Tumor
  • Cervical Adenocarcinoma
  • Cervical Adenosquamous Carcinoma
  • Cervical Small Cell Carcinoma
  • Cervical Squamous Cell Carcinoma, Not Otherwise Specified
  • Childhood Embryonal Rhabdomyosarcoma
  • Childhood Malignant Ovarian Germ Cell Tumor
  • Endometrioid Stromal Sarcoma
  • Gestational Trophoblastic Tumor
  • Malignant Mesothelioma
  • Malignant Ovarian Epithelial Tumor
  • Melanoma
  • Neoplasm of Uncertain Malignant Potential
  • Ovarian Brenner Tumor
  • Ovarian Clear Cell Cystadenocarcinoma
  • Ovarian Serous Cystadenocarcinoma
  • Paget Disease of the Vulva
  • Recurrent Cervical Carcinoma
  • Recurrent Fallopian Tube Carcinoma
  • Recurrent Ovarian Carcinoma
  • Recurrent Ovarian Germ Cell Tumor
  • Recurrent Primary Peritoneal Carcinoma
  • Recurrent Uterine Corpus Carcinoma
  • Recurrent Vaginal Carcinoma
  • Recurrent Vulvar Carcinoma
  • Stage I Ovarian Cancer
  • Stage I Uterine Corpus Cancer
  • Stage I Vaginal Cancer
  • Stage I Vulvar Cancer
  • Stage IA Cervical Cancer
  • Stage IA Fallopian Tube Cancer
  • Stage IA Ovarian Cancer
  • Stage IA Ovarian Germ Cell Tumor
  • Stage IB Cervical Cancer
  • Stage IB Fallopian Tube Cancer
  • Stage IB Ovarian Cancer
  • Stage IB Ovarian Germ Cell Tumor
  • Stage IC Fallopian Tube Cancer
  • Stage IC Ovarian Cancer
  • Stage IC Ovarian Germ Cell Tumor
  • Stage II Ovarian Cancer
  • Stage II Uterine Corpus Cancer
  • Stage II Vaginal Cancer
  • Stage II Vulvar Cancer
  • Stage IIA Cervical Cancer
  • Stage IIA Fallopian Tube Cancer
  • Stage IIA Ovarian Cancer
  • Stage IIA Ovarian Germ Cell Tumor
  • Stage IIB Cervical Cancer
  • Stage IIB Fallopian Tube Cancer
  • Stage IIB Ovarian Cancer
  • Stage IIB Ovarian Germ Cell Tumor
  • Stage IIC Fallopian Tube Cancer
  • Stage IIC Ovarian Cancer
  • Stage IIC Ovarian Germ Cell Tumor
  • Stage III Borderline Ovarian Surface Epithelial-Stromal Tumor
  • Stage III Cervical Cancer
  • Stage III Uterine Corpus Cancer
  • Stage III Vaginal Cancer
  • Stage III Vulvar Cancer
  • Stage IIIA Fallopian Tube Cancer
  • Stage IIIA Ovarian Cancer
  • Stage IIIA Ovarian Germ Cell Tumor
  • Stage IIIA Primary Peritoneal Cancer
  • Stage IIIB Fallopian Tube Cancer
  • Stage IIIB Ovarian Cancer
  • Stage IIIB Ovarian Germ Cell Tumor
  • Stage IIIB Primary Peritoneal Cancer
  • Stage IIIC Fallopian Tube Cancer
  • Stage IIIC Ovarian Cancer
  • Stage IIIC Ovarian Germ Cell Tumor
  • Stage IIIC Primary Peritoneal Cancer
  • Stage IV Borderline Ovarian Surface Epithelial-Stromal Tumor
  • Stage IV Fallopian Tube Cancer
  • Stage IV Ovarian Cancer
  • Stage IV Primary Peritoneal Cancer
  • Stage IV Uterine Corpus Cancer
  • Stage IVA Cervical Cancer
  • Stage IVA Vaginal Cancer
  • Stage IVB Cervical Cancer
  • Stage IVB Vaginal Cancer
  • Stage IVB Vulvar Cancer
  • Uterine Corpus Cancer
  • Uterine Corpus Leiomyosarcoma
  • Vulvar Squamous Cell Carcinoma

Interventions

OTHER

Laboratory Biomarker Analysis

Correlative studies

Sponsors & Collaborators

  • National Cancer Institute (NCI)

    collaborator NIH
  • Gynecologic Oncology Group

    lead NETWORK

Principal Investigators

  • Michael Cibull · NRG Oncology

Eligibility

Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
1992-06-30
Primary Completion
2016-01-31

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00897442 on ClinicalTrials.gov