Minimal Residual Disease Assessment in Colorectal Cancer (MiRDA-C)

Status: Recruiting
Location: See all (10) locations...
Intervention Type: Procedure, Other
Study Type: Observational
SUMMARY

This study investigates if circulating tumor DNA (ctDNA) and other tumor-related molecules/chemicals released in the blood can help doctors predict if colorectal cancer may come back or spread. Tumors shed DNA and other cancer related chemicals into the blood that can be identified and studied further to provide information about the cancer. Information gathered from this study may help researchers better understand if ctDNA found in the blood can predict whether colorectal cancer may come back or spread.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Age ≥ 18 years.

• Histological/cytological confirmation of colorectal adenocarcinoma.

• Patients with any stage colorectal adenocarcinoma deemed potentially eligible for curative intent treatment. Patients with stages II-IV colorectal cancer post-R0 resection may also be enrolled onto the protocol any time before or up to 3 months post-surgery and prior to initiating adjuvant therapy.

• Ability to understand and the willingness to sign a written informed consent document.

• Willing to pursue standard of care surveillance post completion of curative therapies.

• Willing to provide blood samples for correlative research.

Locations
United States
Arizona
Banner - MD Anderson Cancer Center
TERMINATED
Gilbert
Florida
Baptist- MD Anderson Cancer Center
TERMINATED
Jacksonville
Hawaii
The Queen's Medical Center
TERMINATED
Honolulu
Idaho
St. Luke's Cancer Institute
TERMINATED
Boise
New Jersey
Cooper Hospital UNIV MED CTR.
TERMINATED
Camden
Texas
UT Southwestern/Simmons Cancer Center-Dallas
TERMINATED
Dallas
Houston Methodist Cancer Center
TERMINATED
Houston
M D Anderson Cancer Center
RECRUITING
Houston
UT Health San Antonio MD Anderson Cancer Center
TERMINATED
San Antonio
Baylor Scott & White Research Institute
TERMINATED
Temple
Contact Information
Primary
Arvind Dasari
adasari@mdanderson.org
(713) 792-2828
Time Frame
Start Date: 2019-11-22
Estimated Completion Date: 2025-12-31
Participants
Target number of participants: 1000
Treatments
Ancillary-correlative (biospecimen collection)
Patients undergo collection of blood samples at baseline, during each neoadjuvant therapy treatment, prior to surgical resection, and up to 4 times per year for up to 5 years. Patients also undergo collection of tissue sample at time of surgical resection. Patients medical records may also be reviewed.
Related Therapeutic Areas
Sponsors
Leads: M.D. Anderson Cancer Center

This content was sourced from clinicaltrials.gov