Esophageal Squamous Cell Cancer Surveillance With Cytosponge (NCT04192695) | Clinical Trial Compass
CompletedNot Applicable
Esophageal Squamous Cell Cancer Surveillance With Cytosponge
Poland178 participantsStarted 2021-01-01
Plain-language summary
Surveillance and early detection of esophageal squamous cell carcinoma with minimally-invasive Cytospongeâ„¢ cell collection device coupled with molecular biomarkers.
Who can participate
Age range18 Years
SexALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
Patients with esophageal squamous cell cancer (ESCC):
* Patients ≥18 years of with adequate performance status for endoscopy
* Newly diagnosed ESCC suitable for endoscopic or oncological treatment (Rth/Chth)
* Patients currently undergoing oncological treatment (Rth/Chth)
* Consent to provide tissue samples for the study
* Dysphagia grade ≤2 (able to swallow mixed foods and tablets)
Patients at high risk for ESCC:
* Patients ≥18 years of age with adequate performance status for endoscopy
* Prior definitive treatment for head and neck cancer (cancer of the oral cavity, hypopharyngeal cancer, laryngeal carcinoma) and at least 12 months post-therapy (both Rth, Chth, and combination treatment)
* Prior definitive endoscopic treatment for early ESCC in the past (at least 6 months since completion)
* Consent to provide tissue samples for the study
* Dysphagia grade ≤2
Exclusion Criteria (for both groups of patients):
* Patients currently on anticoagulant treatment (warfarin, acenocoumarol) with no possibility of stopping / modification
* Dysphagia grade ≥3 (able to swallow only liquid foods)
* History of myocardial infarction or other cardiovascular event within 6 months of enrolment
* Neurological diseases associated with impaired swallowing
* Patients in long-term care or institutional care (physical, psycho-social disorders, intellectual disability).
What they're measuring
1
Discovery of suitable biomarkers for squamous intraepithelial neoplasia to inform future trials.