TracelT Hydrogel in Localizing Bladder Tumors in Patients Undergoing Radiation Therapy for Bladder Cancer
Primary Purpose
Bladder Carcinoma
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Polyethylene Glycol Hydrogel
Sponsored by
About this trial
This is an interventional treatment trial for Bladder Carcinoma
Eligibility Criteria
Inclusion Criteria:
- Histologically confirmed malignancy of the bladder
- No prior cystectomy
- Treatment plan for bladder must include at least 4 weeks of daily radiation treatment (most patients will receive chemotherapy concurrent with radiation, but this is not required for trial enrollment)
- Patient must undergo TraceIT hydrogel placement within 8 weeks prior to starting radiation therapy for bladder cancer
- Participants must have a complete history and physical examination within 60 days of study entry
- Participants must be able to provide informed consent for treatment and trial participation
- No restrictions on prior treatment to be eligible
Exclusion Criteria:
- Prior cystectomy
- Unable to have TraceIT hydrogel placement < 8 weeks prior to beginning radiation treatment
- Treatment for metastatic bladder cancer
Sites / Locations
- Fred Hutch/University of Washington Cancer Consortium
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Supportive care (TracelT hydrogel)
Arm Description
Patients undergo transurethral resection of bladder tumors and receive TracelT hydrogel via injection. Patients undergo standard of care radiation therapy within 8 weeks of TracelT hydrogel placement.
Outcomes
Primary Outcome Measures
Changes in Interfraction Motion of the Marker Measured by Cone Beam Computed Tomography (CT) and x/y/z Coordinates
Daily changes will be compared across the patient group as well as within each subjects' treatment course.
Changes in Tumor Bed Size and Shape as Delineated by the Hydrogel and Measured by Cone Beam CT and x/y/z Coordinates
Daily changes will be compared across the patient group as well as within each subjects' treatment course. These changes will be tracked during the entire radiation course (typically 4-8 weeks), yielded a distribution of x/y/z positions for each patient.
Secondary Outcome Measures
Daily Dose of Radiation to the PTV as Based on Alignment to the Hydrogel Location Versus Alignment to Whole Bladder Location Versus Alignment to Bony Antonym
Daily pre-radiation imaging will be used to run the radiation treatment plan, to calculate the daily dose to the PTV based on alignment to the hydrogel location, versus alignment to whole bladder location, versus alignment to bony anatomy.
Daily Dose to the Planning Tumor Volume (PTV) Based on Hydrogel Location
Daily pre-radiation imaging will be used to run the radiation treatment plan, to calculate the daily dose to the PTV based on hydrogel location. Total radiation dose to the PTV can then be calculated as the sum of the daily dose.
Number of Participants With Adverse Events Caused by Hydrogel
Graded by the Common Terminology Criteria in Adverse Events version 4.0
Smallest Setup Margin Required for Consistent Coverage of the Gross Tumor Volume (GTV)
Daily pre-radiation imaging will be used to identify the smallest setup margin required for consistent coverage of the GTV, which is likely smaller than the current standard of care setup margin of at least 2 cm around the GTV.
Full Information
NCT ID
NCT03125226
First Posted
April 13, 2017
Last Updated
February 6, 2021
Sponsor
University of Washington
Collaborators
National Cancer Institute (NCI)
1. Study Identification
Unique Protocol Identification Number
NCT03125226
Brief Title
TracelT Hydrogel in Localizing Bladder Tumors in Patients Undergoing Radiation Therapy for Bladder Cancer
Official Title
TraceIT TM Hydrogel Tissue Marker for Patients Receiving Definitive Chemoradiation for Bladder Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
February 2021
Overall Recruitment Status
Completed
Study Start Date
October 5, 2017 (Actual)
Primary Completion Date
January 1, 2020 (Actual)
Study Completion Date
May 18, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Washington
Collaborators
National Cancer Institute (NCI)
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
This pilot clinical trial studies how well TracelT hydrogel works in localizing bladder tumors in patients undergoing radiation therapy for bladder cancer. TracelT hydrogel marks the location of a bladder tumor and makes it more visible during imaging tests. Using TracelT hydrogel tissue marker may help doctors learn more about tumor location and altering radiation dosage for bladder cancer.
Detailed Description
PRIMARY OBJECTIVES:
I. To utilize the TraceIT hydrogel tissue marker in localizing bladder tumors during transurethral resection of bladder tumors (TURBT).
II. To improve identification of gross tumor or tumor bed location in patients receiving chemoradiation treatment for bladder cancers.
SECONDARY OBJECTIVES:
I. To report adverse events surrounding the placement of the TraceIT tissue marker.
II. To calculate the actual dose received by the bladder tumor bed, as delineated by the hydrogel.
III. To compare the dosimetric impact to the tumor bed of daily patient alignment to the pelvic bones, versus alignment to the whole bladder, versus alignment to the hydrogel markers.
IV. To calculate the amount of normal tissue radiation dose decrease achievable without losing tumor coverage, with better tumor targeting with hydrogel placement.
OUTLINE:
Patients undergo transurethral resection of bladder tumors and receive TracelT hydrogel via injection. Patients undergo standard of care radiation therapy within 8 weeks of TracelT hydrogel placement.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bladder Carcinoma
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
12 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Supportive care (TracelT hydrogel)
Arm Type
Experimental
Arm Description
Patients undergo transurethral resection of bladder tumors and receive TracelT hydrogel via injection. Patients undergo standard of care radiation therapy within 8 weeks of TracelT hydrogel placement.
Intervention Type
Device
Intervention Name(s)
Polyethylene Glycol Hydrogel
Other Intervention Name(s)
PEG Hydrogel
Intervention Description
Given TracelT hydrogel via injection
Primary Outcome Measure Information:
Title
Changes in Interfraction Motion of the Marker Measured by Cone Beam Computed Tomography (CT) and x/y/z Coordinates
Description
Daily changes will be compared across the patient group as well as within each subjects' treatment course.
Time Frame
Baseline up to 8 weeks
Title
Changes in Tumor Bed Size and Shape as Delineated by the Hydrogel and Measured by Cone Beam CT and x/y/z Coordinates
Description
Daily changes will be compared across the patient group as well as within each subjects' treatment course. These changes will be tracked during the entire radiation course (typically 4-8 weeks), yielded a distribution of x/y/z positions for each patient.
Time Frame
Baseline up to 8 weeks
Secondary Outcome Measure Information:
Title
Daily Dose of Radiation to the PTV as Based on Alignment to the Hydrogel Location Versus Alignment to Whole Bladder Location Versus Alignment to Bony Antonym
Description
Daily pre-radiation imaging will be used to run the radiation treatment plan, to calculate the daily dose to the PTV based on alignment to the hydrogel location, versus alignment to whole bladder location, versus alignment to bony anatomy.
Time Frame
Up to 8 weeks
Title
Daily Dose to the Planning Tumor Volume (PTV) Based on Hydrogel Location
Description
Daily pre-radiation imaging will be used to run the radiation treatment plan, to calculate the daily dose to the PTV based on hydrogel location. Total radiation dose to the PTV can then be calculated as the sum of the daily dose.
Time Frame
Up to 8 weeks
Title
Number of Participants With Adverse Events Caused by Hydrogel
Description
Graded by the Common Terminology Criteria in Adverse Events version 4.0
Time Frame
Up to 1 year
Title
Smallest Setup Margin Required for Consistent Coverage of the Gross Tumor Volume (GTV)
Description
Daily pre-radiation imaging will be used to identify the smallest setup margin required for consistent coverage of the GTV, which is likely smaller than the current standard of care setup margin of at least 2 cm around the GTV.
Time Frame
Up to 8 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Histologically confirmed malignancy of the bladder
No prior cystectomy
Treatment plan for bladder must include at least 4 weeks of daily radiation treatment (most patients will receive chemotherapy concurrent with radiation, but this is not required for trial enrollment)
Patient must undergo TraceIT hydrogel placement within 8 weeks prior to starting radiation therapy for bladder cancer
Participants must have a complete history and physical examination within 60 days of study entry
Participants must be able to provide informed consent for treatment and trial participation
No restrictions on prior treatment to be eligible
Exclusion Criteria:
Prior cystectomy
Unable to have TraceIT hydrogel placement < 8 weeks prior to beginning radiation treatment
Treatment for metastatic bladder cancer
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jing Zeng
Organizational Affiliation
Fred Hutch/University of Washington Cancer Consortium
Official's Role
Principal Investigator
Facility Information:
Facility Name
Fred Hutch/University of Washington Cancer Consortium
City
Seattle
State/Province
Washington
ZIP/Postal Code
98109
Country
United States
12. IPD Sharing Statement
Learn more about this trial
TracelT Hydrogel in Localizing Bladder Tumors in Patients Undergoing Radiation Therapy for Bladder Cancer
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