Clinical Trial

Dynamic Contrast Enhanced Ultrasound for Predict and Assess Rectal Cancer Response After Neo-adjuvant Chemoradiation - RECT

Study acronym: RECT
Terminated
View on ClinicalTrials.gov →
Why the trial stopped
target number of inclusion not reached
Summary
In recent years the concept of organ sparing treatment in rectal cancer was introduced for selected good responders after neo-adjuvant treatment. In these patients replacement of the standard of care total mesorectal excision (TME) by transanal endoscopic microsurgery (TEM) or omission of surgery after chemoradiation (CRT) was proposed. Before organ sparing treatments could be applied in clinical practice a reliable patient selection procedure has to be available as only good treatment responders after neo-adjuvant therapy are candidates for such adapted therapy. Different imaging modalities have been studied for their ability to distinguish good treatment responders from others. Examples of such imaging modalities with some promising results regarding response assessment are fludeoxyglucosepositron emission tomography (FDG-PET), T2-weighted magnetic resonance imaging (T2w-MRI), dynamic contrast enhanced magnetic resonance imaging and diffusion weighted MR imaging (DW-MRI). Besides these modalities dynamic contrast enhanced ultrasound (D-CEUS) is a new modality used for tissue characterization and therapy response assessment in several tumor locations, like liver tumors and breast cancer. D-CEUS reflect tissue vascular perfusion. For rectal cancer, the value of D-CEUS for pathological response prediction and assessment has never been assessed. Therefore, in this study we assessed D-CEUS to predict and assess pathological response in rectal cancer after neo-adjuvant CRT.
Protocol Amendment History 2 changes
critical Trial status changed: Completed → Terminated 2026-07-31
critical Trial terminated: target number of inclusion not reached 2026-07-31
Trial Details
NCT Number NCT03068403
Lead Sponsor University Hospital, Bordeaux
Conditions Rectal Cancer
Enrollment 2 participants
Start Date 2018-06-18
Primary Completion 2018-11-08 (estimated)
Study Completion 2019-01-08 (estimated)
Updated on ClinicalTrials.gov 2026-07-30