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Cryotherapy for Malignant Dysphagia in Patients With Advanced Esophageal Cancer

Not Applicable
Conditions
Esophageal Adenocarcinoma
Registration Number
NCT02606396
Lead Sponsor
Hunter Holmes Mcguire Veteran Affairs Medical Center
Brief Summary

Esophageal adenocarcinoma (EAC) is one of the few cancers with a rising incidence in the United States, with an estimated 17,000 new cases diagnosed in 2012. Most patients with esophageal cancer present with tumors which are not amenable to surgery and are treated with chemotherapy and radiation. The most common and bothersome symptoms from esophageal cancer is dysphagia (difficulty swallowing). Chemotherapy and radiation are effective in shrinking tumors and allowing patients with EAC to swallow more easily; however it usually takes 1-2 months for swallowing to improve with this treatment.

Another method of shrinking esophageal tumors and allowing for better swallowing is endoscopic spray cryotherapy (freezing the tumor from inside the esophagus with the aid of an endoscope); cryotherapy is a well established method for treating cancerous and pre-cancerous esophageal disease. This is a particularly attractive treatment option, as patients with esophageal cancer usually undergo endoscopy on several occasions before starting treatment in order to biopsy and evaluate the tumor.

The goal of this study is to evaluate the effectiveness of cryotherapy in treating EAC related dysphagia in patients who are getting ready to start chemotherapy and radiation.

In order to do this the investigators are planning to invite patients who are already undergoing endoscopy for pre-chemotherapy evaluation of known EAC. Patients would undergo cryotherapy after the diagnostic portion of the endoscopy has been completed. After the cryotherapy patients will be contacted by phone in order to evaluate change in symptoms, 2 and 4 weeks after cryotherapy.

Detailed Description

Endoscopic spray cryotherapy (EC) is a novel modality for destruction of tissue in the gastrointestinal tract. EC involves the endoscopic application of cryogen \[liquid nitrogen (LN)\], which destroys tissue by rapid freezing and slow thawing. Immediate effects from tissue freezing include failure of cellular metabolism, membrane damage and local ischemia. Delayed effects may include apoptosis of cancer cells and immune mediated tumor destruction. EC has been used for the treatment of mucosal EAC and palliation of malignant dysphagia since 2007 in multiple tertiary centers, including Washington University in St Louis, with positive results. EC is an attractive modality for the palliation of malignant dysphagia in EAC due to the fact that newly diagnosed patients undergo upper endoscopy (EGD) and endoscopic ultrasound (EUS) as part of initial staging; thus EC could be delivered at the time of the staging endoscopy, without burdening the patient with an additional procedure. However, prospective studies on the efficacy of EC in the short term palliation of malignant dysphagia in EAC have not been performed.

Thus, the goal of this pilot study is to evaluate the effectiveness of EC in the short term palliation of malignant dysphagia in patients with unresectable EAC.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
15
Inclusion Criteria
  • Patients >18 years of age with malignant dysphagia due to locally advanced EAC (≥T3 and/or N1) who are undergoing upper endoscopic ultrasound or upper endoscopy for pre-treatment staging or symptom evaluation
Exclusion Criteria
  • Prior esophageal or gastro-esophageal junction surgery.
  • Prior diagnosis of oropharyngeal dysphagia.
  • Prior diagnosis of esophageal achalasia.
  • Esophageal strictures unrelated to EAC
  • Distant metastasis
  • Dysphagia only to solid or semi-solid foods
  • Need for esophageal dilation in order to pass the diagnostic upper endoscope distal to the tumor.
  • Coagulopathy (INR>2, platelets < 50,000)
  • Inability to provide informed consent.
  • Marfan's syndrome

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
Change in dysphagia severity according to validated symptom score2 weeks after cryoablation session
Secondary Outcome Measures
NameTimeMethod
Assessment of pathologic complete response and clinical complete response at the completion of neo-adjuvant chemoradiation number one.Up to 24 weeks

Results of the re-staging PET-CT will be abstracted from the medical record to document presence or absence of a pathologic complete response

Assessment of pathologic complete response and clinical complete response at the completion of neo-adjuvant chemoradiation number two.Up to 24 weeks

Results of the surgical explant will be abstracted from the medical record to document presence or absence of a pathologic complete response.

Ability to maintain oral intake evaluated by a member of the study team utilizing dysphagia assessment and oral intake assessment instruments who will contact each patient at 1-month intervals while the patient receives chemoradiationUp to 12 weeks
Incidence of procedure related adverse events, classified according to the American Society of Gastrointestinal Endoscopy lexicon1 week after each procedure; 2 to 3 weeks after each procedure and 8 weeks after completion of the last cryoablation session

Trial Locations

Locations (1)

Center for Advanced Medicine

🇺🇸

Saint Louis, Missouri, United States

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