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CompletedNCT01525953CRCRT-ECUpdated Feb 3, 2012

Complete Clinical Responders to Definite Chemoradiation in Esophageal Cancer : a Survival Analysis

An observational study in Esophageal Cancer, sponsored by Centre Oscar Lambret. Completed at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2012-02-03.

Sponsored by Centre Oscar Lambret · Observational

Study type
Observational
Model
Cohort
Time perspective
Retrospective
Enrollment
110
Ages
18 Years and older
Sex
All
01

Study summary

The aim of this study is to identify prognostic factors for outcome in patients being complete clinical responders with chemoradiation or radiation for esophageal cancer

02

Conditions studied

  • Esophageal Cancer

Keywords

  • esophageal cancer
  • radiochemotherapy
  • prognosis
03

In context

Esophageal Neoplasms

1,593 studies on the registry are indexed under Esophageal Neoplasms; 461 are open to participants now.

This study's enrollment of 110 is below the median of 200 across 341 observational studies indexed under Esophageal Neoplasms.

Browse Esophageal Neoplasms studies →

Lead sponsor

Centre Oscar Lambret is the lead sponsor of 127 studies on the registry; 13 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Patient treated for esophageal cancer in the Northern France Cancer Center from january 1998 to december 2003

Inclusion criteria

  • localized or locally advanced esophageal cancer
  • patient who underwent definite chemoradiation or radiation
  • patient with complete clinical response

Exclusion criteria

Exclusion Criteria:

  • metastatic disease
05

Study design

Observational model
Cohort
Time perspective
Retrospective
Enrollment
110 participants (actual)

Interventions

  • DrugChemotherapy

    Chemotherapy according to standard

  • RadiationRadiotherapy

    Radiotherapy according to local standard

06

What researchers measure

Primary outcomes

  1. Identification of prognostic factors for overall survival

    Correlation between survival and baseline,clinical and treatment characteristics

    Time frame: From date of treatment until death, assessed up to 10 years

Secondary outcomes

  1. Patterns of treatment failure

    Type of recurrence : local, regional, distant.

    Time frame: From date of treatment until treatment failure, assessed up to 10 years

  2. Disease-free survival

    Time between the end of treatment and the occurence of progression

    Time frame: From date of treatment until progression or death, assessed up to 10 years

07

Study locations

1 site
  • Centre Oscar LAMBRET
    Lille, 59000, France
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 3, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01525953
Lead sponsor
Centre Oscar Lambret
Responsible party
Sponsor
First posted
Feb 3, 2012
Start date
Jan 2012
Primary completion
Jan 2012
Completion
Jan 2012
Last update
Feb 3, 2012

Study contacts

Antoine ADENIS, MD, PhD
principal investigator · Centre Oscar Lambret

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2012. You cannot join it, but the record below documents what was studied.

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