Blood proteins may predict who beats esophageal cancer with chemoradiation
NCT ID NCT00911092
First seen Sep 17, 2026 · Last updated Sep 18, 2026 · Updated 1 time
Summary
Researchers are studying whether protein patterns in the blood can predict which people with esophageal cancer will respond completely to combined chemotherapy and radiation. The trial enrolls about 50 adults with invasive esophageal cancer who receive standard radiochemotherapy. Blood samples are taken before treatment and at set times during and after therapy to analyze proteins. The goal is to link early protein changes to treatment response and one-year outcomes.
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 the protein patterns predict who responds to radiochemotherapy, doctors could tailor treatment earlier and spare non-responders from ineffective therapy.
- What could go wrong
- This small observational study may not find reliable protein markers, and results might not apply to all esophageal cancer patients.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
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50 people
The number who actually took part.
- Start date
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Oct 2007
- Finished
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Dec 2011
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Invasive esophageal carcinoma at any stage (all T, N0 or N1, M0 or M1a), histologically proven * Treated by exclusive concomitant radiochemotherapy * Written informed consent Exclusion Criteria: * Presence of a second uncontrolled cancer * Metastatic carcinoma * Metastatic disease, except cervical lymphnodes... (M1a) * In situ carcinoma * Eso-gastric junction cancer (Siewert II ou III) * Inclusion in a clinical trial with an experimental drug during the study and until 15 weeks after the end of radiotherapy)
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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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CHU - Hopital Charles Nicolle
Rouen, 76031, France
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Centre Eugène Marquis
Rennes, 35042, France
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Centre François BACLESSE
Caen, 14046, France
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Centre Hospitalier Universitaire
Brest, 29200, France
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Centre Oscar Lambret
Lille, 59020, France
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Centre Paul Papin
Angers, 49933, France
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