Ultrasound and Biomarker Tests in Predicting Cancer Aggressiveness in Tissue Samples of Patients With Bladder Cancer



Status:Recruiting
Healthy:No
Age Range:18 - Any
Updated:7/4/2018
Start Date:September 16, 2015
End Date:September 16, 2020
Contact:Ileana Aldana
Email:Ileana.aldana@med.usc.edu
Phone:323-865-0702

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Ultrasound and Biomarker Tests of Bladder Cancer Invasiveness

This research trial studies two types of tests, an ultrasound test and a biomarker test, to
see how well they predict how aggressive (invasive) bladder cancer is in samples from
patients with bladder cancer. The aggressiveness of a tumor means how likely it is to invade
the body and spread. The ultrasound test uses a fluorescent dye and stimulates cells under a
microscope to see how they respond. This may allow doctors to predict how likely the cancer
cells are to spread in the body. The biomarker test uses laboratory testing of samples from
patients to study genes and other molecules that may predict the cancer invasiveness.
Comparing two different ways of predicting cancer aggressiveness may help doctors identify
how well they work, and may eventually allow doctors to predict aggressiveness without
needing to take a biopsy.

PRIMARY OBJECTIVES:

I. To establish an association between bladder cancer disease stage and the level of
invasiveness as measured by a novel ultrasound assay.

II. To establish an association between bladder cancer disease stage and expression of novel
invasiveness biomarkers related to the RE1-silencing transcription factor (REST) gene.

OUTLINE:

Previously collected tumor tissue samples, bladder washings, and urine cells are stained with
calcium dye, washed and immersed in external buffer solution, and then transferred to the
ultrasound imaging system. Tissue, bladder wash cells and urine cells samples are also
analyzed for biomarkers of invasiveness derived from or related to REST gene via quantitative
reverse transcriptase polymerase chain reaction (qRT-PCR), Western blot, and fluorescence in
situ hybridization (FISH).

Inclusion Criteria:

- Patients with a confirmed diagnosis of UCC, having one of the stages (Ta, Tis, T1, and
T2 or higher)

- Patients with UCC who are undergoing a standard procedure to remove cells/tissue from
their bladders (cystoscopy, biopsy, or surgery)

- Ability to understand and the willingness to sign a written informed consent

Exclusion Criteria:

- Patients who have had chemotherapy, radiotherapy, or immunotherapy within 4 weeks
prior to entering the study or those who have not recovered from adverse events due to
agents administered more than 4 weeks earlier
We found this trial at
1
site
1441 Eastlake Ave
Los Angeles, California 90033
(323) 865-3000
Principal Investigator: Andres Weitz
Phone: 323-865-0648
U.S.C./Norris Comprehensive Cancer Center The USC Norris Comprehensive Cancer Center, located in Los Angeles, is...
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mi
from
Los Angeles, CA
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