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Pre-operative MRI of Esophagus Cancer

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

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03347630
Acronym
STIRMCO
Enrollment
60
Registered
2017-11-20
Start date
2017-10-02
Completion date
2019-03-30
Last updated
2017-11-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diagnoses Disease, Esophagus Cancer

Keywords

MRI, oesophagus cancer, Staging

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.

Interventions

DIAGNOSTIC_TESTMRI

Thoraco-abominal MRI

Sponsors

Dromain Clarisse
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Any pathologically proven oesophagus cancer

Exclusion criteria

* MRI contraindication * Pregnant women * cervical esophagus cancer

Design outcomes

Primary

MeasureTime frameDescription
diagnostic performance for staging18 monthsTNM staging

Secondary

MeasureTime frameDescription
Diagnostic performance for staging18 monthsAssessment of rate of Under and overstaging
Prognostic biomarker18 monthscorrelation of MRI data with PFS, morbidity mortality rate and surgical resection
Diagnostic performance to assess tumor response18 monthsCorrelation of changes of ADC values and histological TRG

Countries

Switzerland

Contacts

Primary ContactClarisse Dromain, MD, PhD
clarisse.dromain@chuv.ch0795568369
Backup ContactMarkus Schafer, Pr
markus.schafer@chuv.ch0795561699

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026