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Clinical Trials/NCT03347630
NCT03347630
Unknown
Not Applicable

Prospective Evaluation of MRI in Pre-operative Staging of Esophagus Cancers

Dromain Clarisse1 site in 1 country60 target enrollmentOctober 2, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Esophagus Cancer
Sponsor
Dromain Clarisse
Enrollment
60
Locations
1
Primary Endpoint
diagnostic performance for staging
Last Updated
8 years ago

Overview

Brief Summary

The role of MRI in the management of esophageal cancer remains unclear and poorly studied. Recent technical advances suggest that MRI may become a powerful technique for the initial assessment of esophageal cancer, but also for the evaluation of response to neo-adjuvant treatment before surgery.

This imaging study will be performed prospectively and consecutively in 60 patients included over a 18-month period in patients wîth newly diagnosed esophageal cancer.

The aim of this study is to assess the accuracy of MRI to visualize esophageal tumors, to assess tumor burden and potential contact with adjacent structures as well as associated lymph nodes. If chemotherapy or radio-chemotherapy treatment is indicated before surgery, we will also evaluate whether MRI helps us to better evaluate the response to this treatment in comparison to PET-scan or echo. endoscopy which are the examinations currently performed to evaluate the effectiveness of these treatments.

The images of the MRI exams will be interpreted by 1 expert radiologist with no knowledge of the other imaging modalities and transmitted to the doctors in charge for possible consideration for the treatment.

Patients will then be followed for one year according to clinical management standards to study the data on treatment complications and cancer progression at one year.

The main risk is the administration of a gadolinium chelate-based MRI contrast product used routinely. There is also a risk that the results of the MRI may influence the treatment initially planned for example by canceling a surgical procedure.

Detailed Description

The study will be proppsed consecutively to all patients with a histologically proven diagnosis of esophageal cancer. An MRI examination including morphological sequences (without and with injection of a gadolinium chelate) functional and dynamic will be carried out in all the patients for initial staging in addition to other diagnostic procedure performed in clinical routine in this indication that are the endo-ultrasonography, CT and PET scanner. In patients for whom neo-adjuvant treatment with chemotherapy or radio-chemotherapy will be decided and started, a second MRI will be performed 4 to 6 weeks after the end of the neo-adjuvant treatment. The images of the MR exams will be interpreted by 1 expert radiologist blinded from data of other imaging modalities and transmitted to the doctors in charge of the patient for possible consideration for the treatment. Patients will then be followed for one year according to regular recommandation to assess mortality / morbidity and PFS at 1 year.

Registry
clinicaltrials.gov
Start Date
October 2, 2017
End Date
March 30, 2019
Last Updated
8 years ago
Study Type
Interventional
Study Design
Single Group
Sex
All

Investigators

Sponsor
Dromain Clarisse
Responsible Party
Sponsor Investigator
Principal Investigator

Dromain Clarisse

MD, phD

University of Lausanne Hospitals

Eligibility Criteria

Inclusion Criteria

  • Any pathologically proven oesophagus cancer

Exclusion Criteria

  • MRI contraindication
  • Pregnant women
  • cervical esophagus cancer

Outcomes

Primary Outcomes

diagnostic performance for staging

Time Frame: 18 months

TNM staging

Secondary Outcomes

  • Diagnostic performance for staging(18 months)
  • Diagnostic performance to assess tumor response(18 months)
  • Prognostic biomarker(18 months)

Study Sites (1)

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