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COMPLETED
NCT00911092
PHASE4

Predictive Proteomic Factors of the Response to Concomitant Radiochemotherapy in Esophageal Cancer

Sponsor: Centre Oscar Lambret

View on ClinicalTrials.gov

Summary

The scope of the trial is to predict the early complete clinical response to exclusive concomitant radiochemotherapy in esophageal cancer by the study of the pre- and per- therapeutic proteomic profile.

Official title: Study of Predictive Proteomic Factors of the Response to Exclusive Concomitant Radiochemotherapy in Oesophageal Cancer

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

50

Start Date

2007-10

Completion Date

2011-12

Last Updated

2026-09-17

Healthy Volunteers

No

Interventions

PROCEDURE

Blood sampling

Before any study treatment, 14 days after radiotherapy, 15 weeks after radiotherapy

RADIATION

Radiation

Week 1 to week 5-6 1.8-2 Gys/fraction, 5 days a week for a total of 5 to 6 weeks

DRUG

Chemotherapy (Fluorouracil and Cisplatin)

At weeks 1, 5, 8 and 11 * Day 1 to day 4: Fluorouracil 1 gr/m²/day * Day 1 or 2: Cisplatin 75 mg/m²

Locations (6)

Centre Paul Papin

Angers, France

Centre Hospitalier Universitaire

Brest, France

Centre François BACLESSE

Caen, France

Centre Oscar Lambret

Lille, France

Centre Eugène Marquis

Rennes, France

CHU - Hopital Charles Nicolle

Rouen, France