TrialX API NRG-GI008 Colon Adjuvant Chemotherapy Based on Evaluation of Residual Disease (Circulate-North America).
Study of Chemotherapy Choices Guided by Blood Test Results After Colon Cancer Surgery
Brief description of study
Phase II and III: To compare time to DFS event (recurrence, second primary colorectal can cer or death) in ctDNA (+ve) cohort following resection of colon cancer treated with 5-FU (orcapecitabine) and oxaliplatin x 6 months or 5-FU, oxaliplatin and irinotecan x 6 months.
Eligibility of study
You may be eligible for this study if you meet the following criteria:
- Conditions: Medical Research
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Age: 99 years or below
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Gender: All
TBD
The purpose of this research study is to learn how different chemotherapy treatment plans compare for people who have had colon cancer removed with surgery and who have a positive blood test for remaining cancer signals (called ctDNA, a blood test that looks for tiny pieces of tumor DNA in the blood). The study will compare how long people stay free of the cancer coming back, developing a new colorectal cancer, or dying.
Participants will receive 1 of 2 chemotherapy treatment plans for about 6 months. Both treatment plans use standard chemotherapy medicines, but the combinations are different. The study will track whether participants have a cancer recurrence, a second new colorectal cancer, or death over time.
Who can participate:
People who have had colon cancer removed with surgery may be able to participate if they:
- Have a positive ctDNA blood test after surgery
Study is selecting its participants from a population, or group of people, decided on by the researchers in advance.
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