3-Dimensional Conformal Radiation Therapy in Treating Patients With Bladder Cancer Who Have Undergone Transurethral Resection of the Bladder
Primary Purpose
Bladder Cancer
Status
Unknown status
Phase
Phase 1
Locations
United Kingdom
Study Type
Interventional
Intervention
diagnostic cystoscopy
diffusion-weighted magnetic resonance imaging
implanted fiducial-based imaging
quality-of-life assessment
3-dimensional conformal radiation therapy
image-guided radiation therapy
selective external radiation therapy
Sponsored by
About this trial
This is an interventional treatment trial for Bladder Cancer focused on measuring adenocarcinoma of the bladder, squamous cell carcinoma of the bladder, transitional cell carcinoma of the bladder, recurrent bladder cancer, stage II bladder cancer, stage III bladder cancer, stage IV bladder cancer
Eligibility Criteria
DISEASE CHARACTERISTICS:
Histologically confirmed invasive bladder carcinoma, including the following cellular types:
- Adenocarcinoma
- Transitional cell carcinoma
- Squamous cell carcinoma
Clinical stage G1-3, pT2a-4 disease
- Localized disease
- No bone or visceral metastases
- No lymph node metastases
- Has undergone maximal transurethral resection of the bladder tumor and planning to receive radical radiotherapy
PATIENT CHARACTERISTICS:
- WHO performance status 0-1
- Hemoglobin > 10 g/dL
- WBC > 3,000/mm^3
- Platelet count > 150,000/mm^3
- Creatinine < 120 μmol/L
- Bilirubin < 1.5 times upper limit normal (ULN)
- AST < 1.5 times ULN
- Alkaline phosphatase < 1.5 times ULN
- Not pregnant
- No inflammatory bowel disease or other significant small bowel disease
- Physically fit for radical radiotherapy
- No psychological, familial, sociological, or geographical condition potentially hampering compliance with the study protocol and follow-up schedule
No other malignancy within the past 2 years except adequately treated basal cell carcinoma of the skin or adequately treated carcinoma in situ of the cervix uteri
- Prior superficial transitional cell carcinoma of the bladder allowed
PRIOR CONCURRENT THERAPY:
- See Disease Characteristics
- No prior pelvic surgery
- No bilateral hip replacements compromising accurate radiotherapy planning
- No prior radiotherapy to the pelvis
Sites / Locations
- Royal Marsden - SurreyRecruiting
Outcomes
Primary Outcome Measures
Maximum-tolerated dose
Secondary Outcome Measures
Progression-free survival
Overall survival
Bladder preservation rates
Acute and late toxicity and safety profile
Quality of life
Tumor boost volumes delineated with and without gold seeds
Dose-volume histogram analysis of PTV2 and PTV3 coverage
Change in diffusion coefficient between pre- and post-radiotherapy dwMRI scans
Full Information
NCT ID
NCT01124682
First Posted
May 14, 2010
Last Updated
August 23, 2013
Sponsor
Institute of Cancer Research, United Kingdom
1. Study Identification
Unique Protocol Identification Number
NCT01124682
Brief Title
3-Dimensional Conformal Radiation Therapy in Treating Patients With Bladder Cancer Who Have Undergone Transurethral Resection of the Bladder
Official Title
Image Guided Dose Escalated Adaptive Bladder Radiotherapy
Study Type
Interventional
2. Study Status
Record Verification Date
February 2011
Overall Recruitment Status
Unknown status
Study Start Date
May 2009 (undefined)
Primary Completion Date
April 2016 (Anticipated)
Study Completion Date
undefined (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
Institute of Cancer Research, United Kingdom
4. Oversight
5. Study Description
Brief Summary
RATIONALE: Radiation therapy uses high-energy x-rays to kill tumor cells. Specialized radiation therapy that delivers a high dose of radiation directly to the tumor may kill more tumor cells and cause less damage to normal tissue.
PURPOSE: This phase I trial is studying the side effects and best dose of 3-dimensional conformal radiation therapy in treating patients with bladder cancer who have undergone transurethral resection of the bladder.
Detailed Description
OBJECTIVES:
Primary
To determine the maximum-tolerated dose of external-beam radiotherapy delivered as a tumor boost in patients who have undergone prior transurethral bladder resection for muscle-invasive carcinoma of the bladder.
Secondary
To document progression-free survival and overall survival of these patients.
To evaluate patterns of recurrence and bladder preservation rates following dose-escalated radiotherapy in these patients.
To determine the impact of acute and late toxicity on quality of life in these patients.
To assess the use of gold seeds for tumor boost delineation in these patients.
To evaluate the use of virtual cystoscopy tumor localization in these patients.
To assess coverage of the phase II radiotherapy boost volume on the daily cone-beam images.
To assess coverage of the phase III radiotherapy volume on cone-beam images with selected adaptive strategy.
To evaluate the use of diffusion-weighted MRI (dwMRI) scans in assessing response to radiotherapy.
OUTLINE: This is a dose-escalation study.
Patients undergo a rigid cystoscopy and gold-seed insertion, if clinically appropriate. Approximately 3-5 seeds are inserted into the bladder wall to demarcate the maximum extent of visible tumor or tumor bed via a customized introducer. All patients undergo 3-dimensional conformal radiotherapy once daily, 5 days per week during weeks 1 and 4-7 and once daily, 4-6 days per week during weeks 2 and 3, using a combination of image-guided radiotherapy techniques and a partial bladder radiotherapy boost.
Patients complete quality-of-life questionnaire QOL-30 at baseline, 1 and 3 months, and then annually after completion of study treatment.
After completion of study treatment, patients are followed up at 4, 8, and 12 weeks, every 6 months for 3 years, and then annually for 2 years.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bladder Cancer
Keywords
adenocarcinoma of the bladder, squamous cell carcinoma of the bladder, transitional cell carcinoma of the bladder, recurrent bladder cancer, stage II bladder cancer, stage III bladder cancer, stage IV bladder cancer
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 1
Masking
None (Open Label)
Enrollment
60 (Anticipated)
8. Arms, Groups, and Interventions
Intervention Type
Procedure
Intervention Name(s)
diagnostic cystoscopy
Intervention Type
Procedure
Intervention Name(s)
diffusion-weighted magnetic resonance imaging
Intervention Type
Procedure
Intervention Name(s)
implanted fiducial-based imaging
Intervention Type
Procedure
Intervention Name(s)
quality-of-life assessment
Intervention Type
Radiation
Intervention Name(s)
3-dimensional conformal radiation therapy
Intervention Type
Radiation
Intervention Name(s)
image-guided radiation therapy
Intervention Type
Radiation
Intervention Name(s)
selective external radiation therapy
Primary Outcome Measure Information:
Title
Maximum-tolerated dose
Secondary Outcome Measure Information:
Title
Progression-free survival
Title
Overall survival
Title
Bladder preservation rates
Title
Acute and late toxicity and safety profile
Title
Quality of life
Title
Tumor boost volumes delineated with and without gold seeds
Title
Dose-volume histogram analysis of PTV2 and PTV3 coverage
Title
Change in diffusion coefficient between pre- and post-radiotherapy dwMRI scans
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
DISEASE CHARACTERISTICS:
Histologically confirmed invasive bladder carcinoma, including the following cellular types:
Adenocarcinoma
Transitional cell carcinoma
Squamous cell carcinoma
Clinical stage G1-3, pT2a-4 disease
Localized disease
No bone or visceral metastases
No lymph node metastases
Has undergone maximal transurethral resection of the bladder tumor and planning to receive radical radiotherapy
PATIENT CHARACTERISTICS:
WHO performance status 0-1
Hemoglobin > 10 g/dL
WBC > 3,000/mm^3
Platelet count > 150,000/mm^3
Creatinine < 120 μmol/L
Bilirubin < 1.5 times upper limit normal (ULN)
AST < 1.5 times ULN
Alkaline phosphatase < 1.5 times ULN
Not pregnant
No inflammatory bowel disease or other significant small bowel disease
Physically fit for radical radiotherapy
No psychological, familial, sociological, or geographical condition potentially hampering compliance with the study protocol and follow-up schedule
No other malignancy within the past 2 years except adequately treated basal cell carcinoma of the skin or adequately treated carcinoma in situ of the cervix uteri
Prior superficial transitional cell carcinoma of the bladder allowed
PRIOR CONCURRENT THERAPY:
See Disease Characteristics
No prior pelvic surgery
No bilateral hip replacements compromising accurate radiotherapy planning
No prior radiotherapy to the pelvis
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Robert A. Huddart, MD
Organizational Affiliation
Royal Marsden NHS Foundation Trust
Official's Role
Principal Investigator
Facility Information:
Facility Name
Royal Marsden - Surrey
City
Sutton
State/Province
England
ZIP/Postal Code
SM2 5PT
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Contact Person
Phone
44-20-8661-3457
Email
robert.huddart@icr.ac.uk
12. IPD Sharing Statement
Learn more about this trial
3-Dimensional Conformal Radiation Therapy in Treating Patients With Bladder Cancer Who Have Undergone Transurethral Resection of the Bladder
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