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Bladder Cancer Chemoradiation Using Intensity Modulated Radiation Therapy

Primary Purpose

Bladder Cancer

Status
Terminated
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Helical tomotherapy IMRT
Sponsored by
Ottawa Hospital Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Bladder Cancer focused on measuring Bladder,, Cancer,, Chemoradiation,, IMRT,, tomotherapy

Eligibility Criteria

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

Inclusion Criteria: A pathological diagnosis of pure or predominantly transitional cell bladder carcinoma Adequate Hematology and biochemistry parameters Invasive or treatment refractory non-invasive transitional cell bladder carcinoma OR operable patients who prefer bladder preservation OR inoperable patients. No metastases on CT scan of chest Exclusion Criteria: Patient with contraindication to radical radiotherapy including inflammatory bowel disease or significant irritative bladder symptoms Contraindication to internal iliac arterial catheterization Prior pelvic radiotherapy for other malignancies Prior cytotoxic chemotherapy excepting intravesical agents

Sites / Locations

  • The Ottawa Hospital Regional Cancer Centre

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Helical tomotherapy IMRT

Arm Description

Helical tomotherapy IMRT

Outcomes

Primary Outcome Measures

Acute GI toxicity

Secondary Outcome Measures

Dosimetric evaluation of bowel and pelvic marrow radiation dose, Bladder time organ motion studies, Patterns of recurrence

Full Information

First Posted
July 7, 2006
Last Updated
April 15, 2020
Sponsor
Ottawa Hospital Research Institute
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1. Study Identification

Unique Protocol Identification Number
NCT00350688
Brief Title
Bladder Cancer Chemoradiation Using Intensity Modulated Radiation Therapy
Official Title
Phase II Trial To Evaluate The Potential For Helical Tomotherapy IMRT To Improve Bladder Cancer Chemoradiation
Study Type
Interventional

2. Study Status

Record Verification Date
April 2020
Overall Recruitment Status
Terminated
Why Stopped
More advanced treatments superceded study design
Study Start Date
November 2005 (undefined)
Primary Completion Date
April 2010 (Actual)
Study Completion Date
April 2010 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Ottawa Hospital Research Institute

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
While the gold standard of treatment in invasive bladder cancer is surgical removal of the bladder, it is well accepted that a reasonable alternative is an organ preserving approach. Bladder preservation can be achieved in patients with radiotherapy alone or together with concurrent chemotherapy. This clinical trial will assess the potential of intensity modulated radiation therapy (IMRT) delivered using helical tomotherapy to reduce radiation-induced gastrointestinal toxicity and increase the accuracy of bladder cancer irradiation.
Detailed Description
Patients opting for bladder conservation in Ottawa are currently treated using intra-arterial cisplatin and concurrent radiotherapy using 3D-Conformal radiotherapy. It has been recently reported that while combination chemotherapy with local therapy (surgery or radiation) does modestly increase survival, greater toxicity results. As a precursor to the integration of gemcitabine in the standard chemotherapy regimen at our centre, the current clinical trial is designed to determine if a novel approach to the delivery of intensity modulated radiotherapy (IMRT), namely Helical Tomotherapy, will decrease the toxicity of standard chemoradiation. Chemoradiation will be administered as follows: 3 courses Intra-Arterial Cisplatin 90mg/m2 every 3 weeks and radical radiation delivered as IMRT for a total dose of 60 Gy in 30 daily fractions of 2 Gy per day M-F starting day 15.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bladder Cancer
Keywords
Bladder,, Cancer,, Chemoradiation,, IMRT,, tomotherapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
9 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Helical tomotherapy IMRT
Arm Type
Other
Arm Description
Helical tomotherapy IMRT
Intervention Type
Radiation
Intervention Name(s)
Helical tomotherapy IMRT
Intervention Description
Helical tomotherapy IMRT
Primary Outcome Measure Information:
Title
Acute GI toxicity
Secondary Outcome Measure Information:
Title
Dosimetric evaluation of bowel and pelvic marrow radiation dose, Bladder time organ motion studies, Patterns of recurrence

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: A pathological diagnosis of pure or predominantly transitional cell bladder carcinoma Adequate Hematology and biochemistry parameters Invasive or treatment refractory non-invasive transitional cell bladder carcinoma OR operable patients who prefer bladder preservation OR inoperable patients. No metastases on CT scan of chest Exclusion Criteria: Patient with contraindication to radical radiotherapy including inflammatory bowel disease or significant irritative bladder symptoms Contraindication to internal iliac arterial catheterization Prior pelvic radiotherapy for other malignancies Prior cytotoxic chemotherapy excepting intravesical agents
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Libni Eapen, MD
Organizational Affiliation
Ottawa Hospital Research Institute
Official's Role
Study Director
Facility Information:
Facility Name
The Ottawa Hospital Regional Cancer Centre
City
Ottawa
State/Province
Ontario
ZIP/Postal Code
K1H 8L6
Country
Canada

12. IPD Sharing Statement

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Bladder Cancer Chemoradiation Using Intensity Modulated Radiation Therapy

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