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Cryotherapy for Malignant Dysphagia in Patients With Advanced Esophageal Cancer

Primary Purpose

Esophageal Adenocarcinoma

Status
Unknown status
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Cryotherapy
Esophagogastroduodenoscopy (EGD)
Endoscopic ultrasound (EUS)
Sponsored by
Hunter Holmes Mcguire Veteran Affairs Medical Center
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Esophageal Adenocarcinoma

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Center for Advanced MedicineRecruiting

Outcomes

Primary Outcome Measures

Change in dysphagia severity according to validated symptom score

Secondary Outcome Measures

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 chemoradiation
Assessment of pathologic complete response and clinical complete response at the completion of neo-adjuvant chemoradiation number one.
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.
Results of the surgical explant will be abstracted from the medical record to document presence or absence of a pathologic complete response.
Incidence of procedure related adverse events, classified according to the American Society of Gastrointestinal Endoscopy lexicon

Full Information

First Posted
November 9, 2015
Last Updated
July 17, 2017
Sponsor
Hunter Holmes Mcguire Veteran Affairs Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT02606396
Brief Title
Cryotherapy for Malignant Dysphagia in Patients With Advanced Esophageal Cancer
Official Title
Palliation of Malignant Dysphagia With Spray Cryotherapy in Patients With Advanced Esophageal Cancer: A Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
July 2017
Overall Recruitment Status
Unknown status
Study Start Date
November 2015 (undefined)
Primary Completion Date
June 2018 (Anticipated)
Study Completion Date
June 2018 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hunter Holmes Mcguire Veteran Affairs Medical Center

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Esophageal Adenocarcinoma

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
15 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Procedure
Intervention Name(s)
Cryotherapy
Intervention Description
Cryotherapy employs thermal ablation to treat esophageal cancer and BE. Ablation is achieved by intracellular disruption and ischemia that is produced by freeze-thaw cycles using liquid nitrogen or carbon dioxide
Intervention Type
Procedure
Intervention Name(s)
Esophagogastroduodenoscopy (EGD)
Intervention Description
EGD is a diagnostic procedure that allows the physician to diagnose and treat problems in the upper gastrointestinal (UGI) tract. The doctor uses a long, flexible, lighted tube called an endoscope.
Intervention Type
Procedure
Intervention Name(s)
Endoscopic ultrasound (EUS)
Intervention Description
EUS is a procedure that allows a doctor to obtain images and information about the digestive tract and the surrounding tissue and organs, including the lungs. Ultrasound testing uses sound waves to make a picture of internal organs.
Primary Outcome Measure Information:
Title
Change in dysphagia severity according to validated symptom score
Time Frame
2 weeks after cryoablation session
Secondary Outcome Measure Information:
Title
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 chemoradiation
Time Frame
Up to 12 weeks
Title
Assessment of pathologic complete response and clinical complete response at the completion of neo-adjuvant chemoradiation number one.
Description
Results of the re-staging PET-CT will be abstracted from the medical record to document presence or absence of a pathologic complete response
Time Frame
Up to 24 weeks
Title
Assessment of pathologic complete response and clinical complete response at the completion of neo-adjuvant chemoradiation number two.
Description
Results of the surgical explant will be abstracted from the medical record to document presence or absence of a pathologic complete response.
Time Frame
Up to 24 weeks
Title
Incidence of procedure related adverse events, classified according to the American Society of Gastrointestinal Endoscopy lexicon
Time Frame
1 week after each procedure; 2 to 3 weeks after each procedure and 8 weeks after completion of the last cryoablation session

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Vladimir M Kushnir, MD
Phone
314-362-3685
Email
vkushnir@dom.wustl.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Vladimir M Kushnir, MD
Organizational Affiliation
Washington University School of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Center for Advanced Medicine
City
Saint Louis
State/Province
Missouri
ZIP/Postal Code
63110
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Thomas G Hollander, RN
Phone
314-747-1973
Email
tholland@dom.wustl.edu

12. IPD Sharing Statement

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Cryotherapy for Malignant Dysphagia in Patients With Advanced Esophageal Cancer

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