Overview
- Rationale
Dysphagia is commonly encountered in patients with esophageal carcinoma who are no candidates for treatment with curative intent. It often has a considerable impact on quality of life and can cause malnourishment. Current palliative treatments mainly include esophageal stenting and radiotherapy, but these can be associated with substantial drawbacks such as a high rate of adverse events, fatigue or an untimely/ temporary symptom improvement. Recent studies showed promising results for the use of spray cryotherapy as palliation for dysphagia. Moreover, there are suggestions that cryotherapy has a positive effect on the host's anti-tumor response. However, no data exists on the feasibility, efficacy and safety for cryoballoon therapy in the esophagus. Secondly, cryo-immunologic data in patients with EC is lacking.
- Objective
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- To evaluate the feasibility of cryoballoon ablation in patients with esophageal carcinoma and symptoms of dysphagia. Additionally, efficacy and safety will be assessed.
- To evaluate the effect of cryoballoon ablation on host's anti-tumor response. Study design: Pilot study, Multi-center Prospective Uncontrolled Intervention
Study Study population: Adult patients (≥18 years) with dysphagia due to incurable esophageal carcinoma Intervention (if applicable): Focal cryoballoon ablation of visible tumor during an upper endoscopy. Cryoballoon ablation will be performed for two cycles of 12 seconds. In total, patients will undergo 3 treatment sessions (range 1-3) with an interval of 1-3 weeks based onthe severity of symptoms reported by the patient.
Main study parameters/endpoints:
- - Feasibility of cryoballoon ablation defined as technical success of the procedure
- Safety based on incidence of procedure-related serious adverse events
- Efficacy defined as success rates two weeks after the last cryoablation treatment based on patient reported symptom improvement, and objective evaluation of the esophageal lumen that is free from tumor
- Host's anti-tumor response after cryoballoon ablation based on sequential esophageal tumor biopsies and peripheral blood samples
Eligibility
Inclusion Criteria:
- Age >18 years at time of consent
- Histopathologically-confirmed esophageal / gastroesophageal cancer
- Patients in the palliative setting (with or without (future) systemic chemotherapy)
- Dysphagia defined as a score of ≥2 (able to swallow only semi-solids)
- Signed written informed consent
Exclusion Criteria:
- Alternative etiology for dysphagia
- Inability to pass the ultraslim endoscope
- Severe medical comorbidities precluding endoscopy
- Uncorrected coagulopathy
- Prior distal esophagectomy
- Previous esophageal varices
- Expected survival <6 weeks
- Prior radiotherapy for esophageal cancer
- T4b esophageal cancer
- Incapacitated subjects
- Pregnant or breastfeeding