Biomarkers in Tumor Tissue Samples From Patients With Stage III, Stage IV, or Recurrent Endometrial Cancer

Sponsor
Gynecologic Oncology Group (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT01164735
Collaborator
National Cancer Institute (NCI) (NIH)
169
1

Study Details

Study Description

Brief Summary

This research study is studying biomarkers in tissue samples from patients with stage III, stage IV, or recurrent endometrial cancer. Studying samples of tumor tissue from patients with cancer in the laboratory may help doctors learn more about changes that occur in deoxyribonucleic acid (DNA) and identify biomarkers related to cancer.

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

Detailed Description

PRIMARY OBJECTIVES:
  1. To determine the frequency of topoisomerase 2-alpha (TOPO2A) gene copy number alterations (including deletions, gains, and amplification), immunohistochemical expression, and chromosome 17 polysomy in tumor tissue samples from patients with advanced or recurrent endometrial carcinoma treated with anthracycline-based therapy on Gynecologic Oncology Group (GOG)-0177.

  2. To assess the relationship between TOPO2A gene copy number alterations, TOPO2A protein expression, chromosome 17 polysomy, and human epidermal growth factor receptor 2 (HER2) status in tumor tissue samples from these patients.

  3. To assess the association between TOPO2A status (TOPO2A gene copy number alterations and TOPO2A protein expression), or chromosome 17 polysomy and clinical covariates (e.g., age, race/ethnicity, cell type, histologic grade, disease stage, regimen type).

  4. To assess the association between TOPO2A status or chromosome 17 polysomy with measures of clinical outcome including response, progression-free survival, and overall survival of patients treated with this regimen.

  5. To evaluate the potential identification of cut points for TOPO2A protein expression with potential prognostic value in patients treated with this regimen.

OUTLINE:

Archived tumor tissue samples are analyzed for topoisomerase 2-alpha gene alteration and expression and chromosome 17 polysomy by fluorescent in situ hybridization (FISH) and immunohistochemistry (IHC). Clinical information associated with each endometrial carcinoma sample (e.g., age, race/ethnicity, cell type, histologic grade, disease stage, and regimen type) is also collected.

Study Design

Study Type:
Observational
Anticipated Enrollment :
169 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
Topoisomerase 2-Alpha (TOPO2A) Genomic Alterations and Immunohistochemical Expression as Well as Chromosome 17 Polysomy in Advanced or Recurrent Endometrial Carcinoma Treated With Anthracycline-Based Therapy
Study Start Date :
Jan 1, 2100
Anticipated Primary Completion Date :
Jan 1, 2100

Arms and Interventions

Arm Intervention/Treatment
Correlative studies

Archived tumor tissue samples are analyzed for topoisomerase 2-alpha gene alteration and expression and chromosome 17 polysomy by FISH and IHC. Clinical information associated with each endometrial carcinoma sample (e.g., age, race/ethnicity, cell type, histologic grade, disease stage, and regimen type) is also collected.

Other: Laboratory Biomarker Analysis
Correlative studies

Outcome Measures

Primary Outcome Measures

  1. Overall survival [From enrollment on GOG-0177 to death (regardless of cause) or to the date of last contact for women who were alive, assessed up to 5 years]

    The Kaplan-Meier method will be used to estimate and plot the unadjusted survival and progression-free survival time distributions by TOPO2A expression and amplification status.

Secondary Outcome Measures

  1. Clinical response (complete or partial response) [Up to 5 years]

    Logistic regression modeling will be used to explore the relationship between clinical response to treatment and both TOPO2A expression and amplification.

  2. Progression-free survival [From enrollment on GOG-0177 to disease progression or death, or to the date of last contact for women who were still alive with no evidence of disease progression, assessed up to 5 years]

    The Kaplan-Meier method will be used to estimate and plot the unadjusted survival and progression-free survival time distributions by TOPO2A expression and amplification status.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Chemotherapy-naïve women with histologically documented measurable Stage III, Stage IV or recurrent endometrial carcinoma with known HER2 status who participated in Gynecologic Oncology Group (GOG)-0177 are eligible

  • Patients must have given permission for their archival formalin-fixed, paraffin-embedded primary, metastatic or recurrent tumor to be submitted and used for GOG-0177, and at least one to three unstained slides must be available for FISH analysis of TOPO2A and CEP17 and immunohistochemical staining for TOPO2A

Exclusion Criteria:
  • Women who were not eligible or evaluable on GOG-0177

  • Patients who do not have at least one unstained slide archival formalin-fixed, paraffin-embedded primary, metastatic or recurrent tumor available for fluorescence in situ hybridization (FISH) analysis of TOPO2A and CEP17 or immunohistochemical expression of TOPO2A

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: Tatyana Grushko, Gynecologic Oncology Group

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Gynecologic Oncology Group
ClinicalTrials.gov Identifier:
NCT01164735
Other Study ID Numbers:
  • GOG-8013
  • NCI-2011-02245
  • CDR0000681556
  • GOG-8013
  • GOG-8013
  • GOG-8013
  • U10CA027469
First Posted:
Jul 19, 2010
Last Update Posted:
Jun 8, 2015
Last Verified:
Jun 1, 2015
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 8, 2015