Study of Blood and Cheek Cell Samples From Patients With Glioma

Sponsor
University of California, San Francisco (Other)
Overall Status
Completed
CT.gov ID
NCT01009307
Collaborator
National Cancer Institute (NCI) (NIH)
1,709
1

Study Details

Study Description

Brief Summary

RATIONALE: Studying samples of blood and tissue from patients with cancer in the laboratory may help doctors learn more about changes that occur in DNA and identify biomarkers related to cancer. It may also help doctors predict how patients will respond to treatment.

PURPOSE: This research study is looking at blood and cheek cell samples from patients with glioma.

Condition or Disease Intervention/Treatment Phase
  • Genetic: polymorphism analysis
  • Other: laboratory biomarker analysis
  • Other: medical chart review

Detailed Description

OBJECTIVES:

Primary

  • Determine factors related to glioma survival in patients from two population-based case series collected in the San Francisco Bay Area between August 1991 and April 1994 (series 1) and May 1997 and August 1999 (series 2).

Secondary

  • Determine vital status for 879 patients in the two San Francisco Bay Area population-based series through July 2004.

  • Determine survival as a function of established, potential, and yet unstudied prognostic indicators.

  • Gather data to validate results from this study with information from adult glioma patients enrolled prospectively at the UCSF-Neuro-Oncology clinic and through series 3 of the San Francisco Bay Area Adult Glioma Study; incorporate results from this study and other components of the SPORE into ongoing clinical investigations at the Brain Tumor Research Center and Neuro-Oncology Service at UCSF.

  • Using funding from the organization Accelerate Brain Cancer Cure (ABC2), genotype several thousand single nucleotide polymorphisms (SNPs) from some study participants; assess these SNPs for potential relationship to glioma survival.

OUTLINE: Medical records of patients registered to the California Cancer Registry or the Northern California Cancer Center SEER are reviewed for mortality and treatment information related to the brain tumor. Blood and buccal specimens are collected from patients with newly diagnosed disease who are being seen at the UCSF Neuro-Oncology Service. The specimens are used for polymorphism and tumor marker studies and other pertinent data. Tumor specimens and treatment information related to the brain tumor are also collected from the SPORE Tissue Core.

Additional tumor makers are studied, including: chromosome 1p/19q, 7q studies; DNA repair and oxidative metabolism polymorphisms; and up to 2 tumor markers and 2 constitutive genotyping studies.

Study Design

Study Type:
Observational
Actual Enrollment :
1709 participants
Official Title:
San Francisco Bay Area Adult Glioma Prognosis Study Protocol
Study Start Date :
Oct 1, 2001
Actual Primary Completion Date :
Jul 1, 2006

Outcome Measures

Primary Outcome Measures

  1. Factors related to glioma survival []

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 120 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
DISEASE CHARACTERISTICS:
  • Diagnosis of glioma

  • Meets 1 of the following criteria:

  • Participant in the Survival study of San Francisco Bay Area Adult Glioma Study (SFBAAGS) Series 1 and 2

  • Treated by UCSF Neuro-Oncology Service; diagnosed between Nov. 1, 2001 and June 30, 2006 and seen between Aug. 1, 2002 and June 30, 2006

  • Participant in SFBAAGS Series 3 (not seen at UCSF Neuro-Oncology Service) diagnosed between Nov. 1, 2001 and Oct. 31, 2004

PATIENT CHARACTERISTICS:
  • Not specified
PRIOR CONCURRENT THERAPY:
  • Not specified

Contacts and Locations

Locations

Site City State Country Postal Code
1 UCSF Helen Diller Family Comprehensive Cancer Center San Francisco California United States 94115

Sponsors and Collaborators

  • University of California, San Francisco
  • National Cancer Institute (NCI)

Investigators

  • Study Chair: Margaret Wrensch, University of California, San Francisco

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of California, San Francisco
ClinicalTrials.gov Identifier:
NCT01009307
Other Study ID Numbers:
  • CDR0000437072
  • UCSF-H6539-04956-13A
First Posted:
Nov 6, 2009
Last Update Posted:
Jul 22, 2019
Last Verified:
Jul 1, 2019

Study Results

No Results Posted as of Jul 22, 2019