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Predictive Proteomic Factors of the Response to Concomitant Radiochemotherapy in Esophageal Cancer (COL06-13)

C

Centre Oscar Lambret

Status and phase

Completed
Phase 4

Conditions

Esophageal Cancer

Treatments

Drug: Chemotherapy (Fluorouracil and Cisplatin)
Procedure: Blood sampling
Radiation: Radiation

Study type

Interventional

Funder types

Other

Identifiers

NCT00911092
2006-13

Details and patient eligibility

About

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.

Full description

Further informations will be provided by Centre Oscar Lambret.

Enrollment

50 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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)

Trial contacts and locations

6

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Data sourced from clinicaltrials.gov

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