Blood test may predict chemo success in colorectal cancer
NCT ID NCT01596790
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at whether a new blood test called EPISPOT can predict how well chemotherapy works in people with metastatic colorectal cancer. Researchers measured circulating tumor cells in 168 patients before and during treatment. The goal was to see if early changes in these cells could help doctors personalize therapy.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this blood test could help doctors choose the best first-line treatment for metastatic colorectal cancer patients.
- What could go wrong
- This is an observational study, not a treatment trial. The test may not prove reliable enough to change clinical practice.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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168 people
The number who actually took part.
- Started
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Apr 2012
- Finished
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Sep 2019
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age \> 18 years * Colon or rectum adenocarcinoma (based on the histology) * Visceral metastases (synchronous and/or metachronous) * Metastatic disease measurable with the RECIST 1.1 criteria * WHO performance status 0, 1 or 2 * Life expectancy\>3 months when starting the treatment * Chemotherapy in metastatic 1rst line combining a protocol of conventional chemotherapy combining 5-FU and IRINOTECAN (FOLFIRI, XELIRI) associated with bevacizumab * Follow-up of at least one year * Collection of the written consent * Social security affiliation Exclusion Criteria: * 2nd line chemotherapy and beyond * History of other cancers considered not cured * Active and progressive infection or other serious disease that may not allow the patient to receive the treatment * refusal to participate * Patient unable to express his consent * Pregnant women * Patient unable to be followed-up for at least one year * Current participation to another clinical trial * Patients under guardianship * Vulnerable people protected by the law
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Medical Oncology, CHU St Eloi
Montpellier, 34090, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Can a targeted drug boost chemotherapy in advanced colorectal cancer?
- New antibody aims to preserve immune checkpoint while fighting cancer
- Two-Step PET scan aims to spot hidden colorectal cancer spread
- Can a targeted drug conjugate outsmart advanced colorectal cancer?
- Can an antimalarial drug boost immunotherapy against colorectal cancer?