- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00900341
Studying Tumor Tissue Samples From Patients With Soft Tissue Sarcoma
LABORATORY STUDIES OF SOFT TISSUE SARCOMAS
RATIONALE: Studying samples of tumor 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.
PURPOSE: This research study is looking at tumor tissue samples from patients with soft tissue sarcoma.
Study Overview
Status
Conditions
Detailed Description
OBJECTIVES:
- To develop a pilot program for the collection, archiving, and experimental analyses of soft tissue sarcomas (STS).
- To obtain STS tumors from cancer patients undergoing tumor removal or core needle biopsies.
- To evaluate cellular and molecular factors involved in STS oncogenesis by studying samples derived from human tumor specimens.
- To develop an accompanying bioinformatics database of the demographics of STS patients from which tumor specimens are derived for experimental study.
OUTLINE: Tumor tissue samples are analyzed for gene and protein expression by cDNA microarray analysis, RT-PCR, immunohistochemistry, in vitro transformation assays, RNA interference, and Western blot or immunoprecipitation.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Arizona
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Tucson, Arizona, United States, 85724-5024
- Arizona Cancer Center at University of Arizona Health Sciences Center
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
DISEASE CHARACTERISTICS:
Meets one of the following criteria:
- Patients with soft tissue sarcoma (STS) undergoing evaluation, treatment, and/or follow-up at the Arizona Cancer Center or University Medical Center
- Patients undergoing surgical treatment for STS removal or core needle biopsy for medically indicated diagnostic or therapeutic purposes
PATIENT CHARACTERISTICS:
- Not specified
PRIOR CONCURRENT THERAPY:
- Not specified
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Identification of molecular targets that would improve the diagnosis, prognosis, and/or treatment of STS
Time Frame: 3 months
|
3 months
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Lee D. Cranmer, MD, PhD, University of Arizona
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 05-0509-04
- P30CA023074 (U.S. NIH Grant/Contract)
- UARIZ-HSCA0535 (Other Identifier: CDR0000597591)
- UARIZ-17879
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