Endoesophageal Brachytherapy for Patients With Esophageal Cancer
Primary Purpose
Esophageal Cancer
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Endoesophageal Brachytherapy
Sponsored by
About this trial
This is an interventional supportive care trial for Esophageal Cancer focused on measuring brachytherapy, multichannel balloon applicator
Eligibility Criteria
Inclusion Criteria:
- Biopsy-proved esophageal adenocarcinoma or squamous cell carcinoma
- Disease that can be encompassed in the radiotherapy treatment field
- Women of childbearing potential must practice adequate contraception
- Subjects must have the ability to understand and the willingness to sign a written informed consent document
Exclusion Criteria:
- Concurrent chemotherapy at the time of brachytherapy treatments
- Tracheal or bronchial involvement
- Cervical esophagus location
- Stenosis that cannot be bypassed or dilated to allow for applicator placement
- Not willing or unable to provide informed consent
- History of esophageal fistula
Sites / Locations
- Cleveland Clinic, Case Comprehensive Cancer Center
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
brachytherapy with multichannel balloon applicator
Arm Description
6 channel balloon re-positioning, multichannel brachytherapy applicator used to deliver localized radiation therapy to esophageal tumors
Outcomes
Primary Outcome Measures
Dose of Radiation Delivered to 90% of Tumor Volume (D90)
Percent of prescription dose received by 90% of PTV (planning target volume)
Percent Volume of the Tumor Receiving the Prescription Dose (V100)
Percent volume of the tumor receiving 100% of the prescription dose calculated as the mean from the total weekly HDR brachytherapy treatment plans
Secondary Outcome Measures
Radiation Treatment Volume
Volume of tissue, both tumor plus normal tissue volume, receiving 100% of the prescription dose
Dose of Radiation to Organ at Risk (Bronchus)
Dose to 1cc volume of the trachea-mainstem bronchus calculated as the mean dose from the total weekly HDR brachytherapy treatment plans for the 4 participants who had tumors in proximity to the trachea or mainstem bronchus.
Dose of Radiation to Organ at Risk (Heart)
Dose to 1 cc volume of the heart calculated as the mean dose from the total weekly HDR brachytherapy treatment plans for the 4 participants who had tumors in proximity to the heart.
Dose of Radiation to Organ at Risk (Aorta)
Dose to 1 cc volume of the aorta calculated as the mean dose from the total weekly HDR brachytherapy treatment plans for the 6 participants who had tumors in proximity to the aorta.
Tumor Response Based on Resist Criteria
Tumor response determined by endoscopic evaluation of tumor at time of last brachytherapy treatment. Endoscopic CR is defined as no visible tumor at end of treatment -on endoscopy exam and PR is defined as a persistent tumor at the end of treatment.
Number of Participants With Esophageal Ulceration
Presence of an ulceration of the mucosa in area of brachytherapy treatment
Number of Participants With Esophageal Fistula
Presence of a fistula between the esophagus and trachea, mainstem bronchus or mediastinum
Number of Particiapants With Esophageal Stricture
Presence of an esophageal stricture
Number of Participants With the Need for Dilation
Number of participants with the need for esophageal dilation
Full Information
NCT ID
NCT03335813
First Posted
November 3, 2017
Last Updated
May 17, 2022
Sponsor
Case Comprehensive Cancer Center
1. Study Identification
Unique Protocol Identification Number
NCT03335813
Brief Title
Endoesophageal Brachytherapy for Patients With Esophageal Cancer
Official Title
Endoesophageal Brachytherapy for Patients With Esophageal Cancer: A Balloon Repositioning, Multichannel Radiation Applicator for Optimizing Treatment Delivery
Study Type
Interventional
2. Study Status
Record Verification Date
May 2022
Overall Recruitment Status
Completed
Study Start Date
March 6, 2018 (Actual)
Primary Completion Date
November 14, 2020 (Actual)
Study Completion Date
December 8, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Case Comprehensive Cancer Center
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Depending upon the cancer stage, esophageal cancer can be treated with surgery, chemotherapy, radiation therapy, or a combination of these modalities. Sometimes in addition to external radiation therapy or instead of external radiation therapy, select patients with esophageal cancer may benefit from localized radiation to the tumor, called esophageal brachytherapy. There are many different radiation techniques and delivery approaches for this type of specialized radiation therapy, and the purpose of this document is to provide a written summary of an innovative delivery method.
Detailed Description
Primary Objective Pilot study of multichannel endoesophageal brachytherapy applicator to determine dose distribution and conformality of a 6 channel balloon repositioning applicator.
Secondary Objective(s)
To collect data in order to show how the 6-tube endoesophageal brachytherapy technique will be an improvement (more conformed dose distribution) over a previously designed 3-tube endoesophageal brachytherapy technique in patients who are candidates for esophageal brachytherapy
To evaluate acute toxicity of novel endoesophageal brachytherapy applicator.
Study Design
This innovative study will be an improvement over a previously designed 3-tube endoesophageal brachytherapy technique in patients who are candidates for esophageal brachytherapy. The brachytherapy planning process will utilize a novel multichannel balloon applicator.
The initial treatment session will occur after the patient has been found to be eligible, the consent form has been completed, and the treatment plan has been created. The patient will undergo subsequent weekly treatments for 3 to 6 weeks after the initial treatment.
The subject will be expected to participate in the trial throughout its entirety. The participation period is 6 months of which the patient will be evaluated and seen at months 3 and 6.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Esophageal Cancer
Keywords
brachytherapy, multichannel balloon applicator
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
7 (Actual)
8. Arms, Groups, and Interventions
Arm Title
brachytherapy with multichannel balloon applicator
Arm Type
Experimental
Arm Description
6 channel balloon re-positioning, multichannel brachytherapy applicator used to deliver localized radiation therapy to esophageal tumors
Intervention Type
Device
Intervention Name(s)
Endoesophageal Brachytherapy
Intervention Description
Balloon repositioning, multichannel brachytherapy applicator which has 6 channels instead of 3-tubes which will be used to deliver localized radiation
Primary Outcome Measure Information:
Title
Dose of Radiation Delivered to 90% of Tumor Volume (D90)
Description
Percent of prescription dose received by 90% of PTV (planning target volume)
Time Frame
Up to 6 months of follow-up
Title
Percent Volume of the Tumor Receiving the Prescription Dose (V100)
Description
Percent volume of the tumor receiving 100% of the prescription dose calculated as the mean from the total weekly HDR brachytherapy treatment plans
Time Frame
Up to 6 months of follow-up
Secondary Outcome Measure Information:
Title
Radiation Treatment Volume
Description
Volume of tissue, both tumor plus normal tissue volume, receiving 100% of the prescription dose
Time Frame
Up to 6 cycles (6 weeks) of treatment
Title
Dose of Radiation to Organ at Risk (Bronchus)
Description
Dose to 1cc volume of the trachea-mainstem bronchus calculated as the mean dose from the total weekly HDR brachytherapy treatment plans for the 4 participants who had tumors in proximity to the trachea or mainstem bronchus.
Time Frame
Up to 6 months of follow-up
Title
Dose of Radiation to Organ at Risk (Heart)
Description
Dose to 1 cc volume of the heart calculated as the mean dose from the total weekly HDR brachytherapy treatment plans for the 4 participants who had tumors in proximity to the heart.
Time Frame
Up to 6 months of follow-up
Title
Dose of Radiation to Organ at Risk (Aorta)
Description
Dose to 1 cc volume of the aorta calculated as the mean dose from the total weekly HDR brachytherapy treatment plans for the 6 participants who had tumors in proximity to the aorta.
Time Frame
Up to 6 months of follow-up
Title
Tumor Response Based on Resist Criteria
Description
Tumor response determined by endoscopic evaluation of tumor at time of last brachytherapy treatment. Endoscopic CR is defined as no visible tumor at end of treatment -on endoscopy exam and PR is defined as a persistent tumor at the end of treatment.
Time Frame
Up to 6 months of follow-up
Title
Number of Participants With Esophageal Ulceration
Description
Presence of an ulceration of the mucosa in area of brachytherapy treatment
Time Frame
Up to 6 cycles (6 weeks) of treatment
Title
Number of Participants With Esophageal Fistula
Description
Presence of a fistula between the esophagus and trachea, mainstem bronchus or mediastinum
Time Frame
Up to 6 cycles (6 weeks) of treatment
Title
Number of Particiapants With Esophageal Stricture
Description
Presence of an esophageal stricture
Time Frame
Up to 6 cycles (6 weeks) of treatment
Title
Number of Participants With the Need for Dilation
Description
Number of participants with the need for esophageal dilation
Time Frame
Up to 6 cycles (6 weeks) of treatment
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Biopsy-proved esophageal adenocarcinoma or squamous cell carcinoma
Disease that can be encompassed in the radiotherapy treatment field
Women of childbearing potential must practice adequate contraception
Subjects must have the ability to understand and the willingness to sign a written informed consent document
Exclusion Criteria:
Concurrent chemotherapy at the time of brachytherapy treatments
Tracheal or bronchial involvement
Cervical esophagus location
Stenosis that cannot be bypassed or dilated to allow for applicator placement
Not willing or unable to provide informed consent
History of esophageal fistula
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
John F Greskovich, MD
Organizational Affiliation
Cleveland Clinic, Case Comprehensive Cancer Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cleveland Clinic, Case Comprehensive Cancer Center
City
Weston
State/Province
Florida
ZIP/Postal Code
33331
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Endoesophageal Brachytherapy for Patients With Esophageal Cancer
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