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Spots Global Cancer Trial Database for Collection of Blood, Urine, and Stool to Monitor MetastaticColorectal Cancers

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Trial Identification

Brief Title: Collection of Blood, Urine, and Stool to Monitor MetastaticColorectal Cancers

Official Title: A Pilot Study of Monitoring Metastatic Colorectal Cancers With Liquid Biopsies

Study ID: NCT03563651

Study Description

Brief Summary: This trial studies the monitoring of therapy and progression by collecting blood, urine, and stool from participants with colorectal cancer that has spread to other places in the body or cannot be removed by surgery. Studying samples of blood, urine, and stool from participants with colorectal cancer in the laboratory may help doctors identify and learn more about biomarkers related to cancer.

Detailed Description: PRIMARY OBJECTIVES: I. Detection of mutated Kras in urine specimen of patients with Kras mutated metastatic colon cancer on first, second, or third line therapy. II. Detection of new Kras in urine in patients without Kras mutated metastatic colon cancer on therapy which includes anti-EGFR antibodies (cetuximab or panitumumab). SECONDARY OBJECTIVES: I. Changes of the stool microbiome with chemotherapy and at progression of the disease. DESCRIPTIVE OBJECTIVES: I. Changes in the quantity of mutated Kras, Braf or PI3K in urine deoxyribonucleic acid (DNA) over the cycles of first line therapy. II. Associations between the quantity of mutated Kras, Braf or PI3K in urine DNA, molecular make up of circulating tumor cells (CTCs), cell free DNA and progression over the course of first line therapy. III. Feasibility of detection of exosome in the plasma of colorectal cancer patients on first line chemotherapy in Dr. Fabbri?s lab at Children?s Hospital Los Angeles. IV. Feasibility of detection of tumor DNA in the plasma of colorectal cancer patients on first line chemotherapy. OUTLINE: Participants undergo collection of blood and urine at baseline, on day 1 of courses 1, 2, and 3, at restaging, and at disease progression. Participants may undergo collection of stool at baseline, on day 1 of course 2, and at disease progression. Participants also undergo biopsy within 4 weeks of disease progression.

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

USC / Norris Comprehensive Cancer Center, Los Angeles, California, United States

Contact Details

Name: Afsaneh Barzi, MD

Affiliation: University of Southern California

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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