ClinicalTrials.Veeva

Menu

Research Study in Patients With Advanced Ovarian Epithelial Cancer

G

Gynecologic Oncology Group (GOG)

Status

Withdrawn

Conditions

Ovarian Serous Surface Papillary Adenocarcinoma
Ovarian Serous Cystadenocarcinoma
Stage IIIA Ovarian Cancer
Stage IV Ovarian Cancer
Stage IIIB Ovarian Cancer
Stage IIIC Ovarian Cancer

Treatments

Other: Laboratory Biomarker Analysis
Genetic: Comparative Genomic Hybridization
Genetic: Polymerase Chain Reaction

Study type

Observational

Funder types

NETWORK
NIH

Identifiers

NCT00053235
CDR0000269315
NCI-2009-00612 (Registry Identifier)
GOG-8004 (Other Identifier)

Details and patient eligibility

About

This research trial studies tissue samples from patients with ovarian cancer in the laboratory. Analyzing tissue samples from patients in the laboratory may help doctors learn more about cancer.

Full description

OBJECTIVES:

I. Utilize array comparative genomic hybridization and Taqman analyses, a quantitative genomic polymerase chain reaction, to validate the observation that a gain in chromosome 8q is predictive of shorter progression-free survival in patients with primary grade 2 or grade 3 advanced serous papillary ovarian cancer.

II. Utilize these analyses to determine whether a gain in chromosome 8q is predictive of worse overall survival in these patients.

III. Utilize these analyses to determine whether other previously identified chromosomal changes (3q gain, 7q gain, 16q loss, and 17pter-q21 loss) predict outcome in these patients and the association between these changes and clinical characteristics.

IV. Utilize these analyses to identify up to 5 additional chromosomal changes and their association that may predict outcome (progression-free and overall survival) in these patients.

OUTLINE:

Genomic DNA is isolated from optimal cutting temperature (OCT)-embedded tissue and analyzed using comparative genomic hybridization. The chromosomal changes identified by this method are compared to those identified using the Taqman method, a quantitative genomic polymerase chain reaction analysis. Chromosome 8q is of specific interest. Other chromosomal changes may be detected in chromosomes 3q, 7q, 16q, and/or 17pter-q21.

Sex

Female

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Stage III or IV, high-grade (grade 2 or 3) ovarian cancers

    • No borderline or low-grade (grade 1) tumors

    • Tissue from predominately serous ovarian cancer only

      • No clear cell, endometrioid, mucinous, transitional cell, or mixed without predominant serous component
  • Tissue obtained during prior optimal or suboptimal cytoreductive surgery

  • Must be enrolled on GOG-0136 and a GOG front-line paclitaxel/platinum chemotherapy trial

  • Frozen tissue and hematoxylin-eosin stained section from the ovary obtained at initial surgery

  • Performance status - GOG 0-2

Trial design

0 participants in 1 patient group

Ancillary-Correlative
Description:
Genomic DNA is isolated from OCT-embedded tissue and analyzed using comparative genomic hybridization. The chromosomal changes identified by this method are compared to those identified using the Taqman method, a quantitative genomic polymerase chain reaction analysis. Chromosome 8q is of specific interest. Other chromosomal changes may be detected in chromosomes 3q, 7q, 16q, and/or 17pter-q21.
Treatment:
Genetic: Polymerase Chain Reaction
Other: Laboratory Biomarker Analysis
Genetic: Comparative Genomic Hybridization

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems