search
Back to results

3D-Conformal Radiation vs Helical Tomotherapy in Prostate Cancer

Primary Purpose

Prostate Cancer

Status
Unknown status
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Arm B: Helical Tomotherapy Intensity Modulated Radiotherapy
Arm A: 3D-Conformal Radiation
Sponsored by
Ottawa Hospital Research Institute
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Prostate Cancer focused on measuring prostate, IMRT, tomotherapy, radiation, cancer

Eligibility Criteria

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

Inclusion Criteria: A pathologic diagnosis of adenocarcinoma of the prostate Age greater than 18 years ECOG performance status of 2 or less. Presence of any of the following high risk features: Clinical stage cT3-4 or Gleason score 8-10 or Pre-treatment PSA > 20ng/ml or Clinical N1/N2 or pathologic N1/N2 Exclusion Criteria: Patients with contraindication to radical radiation therapy including inflammatory bowel disease Prior or active malignancy except non-melanoma skin carcinoma within 5 years of the diagnosis of prostate cancer Prior pelvic radiotherapy for other malignancies Prior cytotoxic chemotherapy Prior orchiectomy, radical prostatectomy, cryotherapy or thermal ablation therapy for prostate cancer

Sites / Locations

  • The Ottawa Hospital Regional Cancer Centre

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Experimental

Arm Label

Arm A: 3D-Conformal Radiation

Arm B: Helical Tomotherapy Intensity Modulated Radiotherapy

Arm Description

Intervention: Standard radiation treatment for high risk prostate cancer. Once daily Monday to Friday for 8 weeks. 3DCRT 7800 cGY/39 Fractions/ STD Technique* Initial 4F 3DCRT to Nodes/ Prostate + Seminal Vesicles 4,600 cGy/23 Boost 6 F 3DCRT to Prostate 3,200 cGy/16

Intervention: Helical Tomotherapy Intensity Modulated Radiotherapy (IMRT) once daily Monday to Friday for 8 weeks. IMRT using Helical Tomotherapy* 7800 cGY/39 Fractions Boost IMRT to Prostate 3,200 cGy/16

Outcomes

Primary Outcome Measures

Late rectal toxicity from radiotherapy of the prostate
Outcome measurements will be determined by physical exam and bloodwork.

Secondary Outcome Measures

Acute rectal toxicity, Acute and late bladder toxicity, Disease specific survival at 5 years, Biochemical relapse free survival at 5 years, Local control rates at 5 years, Quality of Life
Outcome measurements will be determined by physical exam and bloodwork.

Full Information

First Posted
May 15, 2006
Last Updated
April 15, 2020
Sponsor
Ottawa Hospital Research Institute
search

1. Study Identification

Unique Protocol Identification Number
NCT00326638
Brief Title
3D-Conformal Radiation vs Helical Tomotherapy in Prostate Cancer
Official Title
Randomized Phase III Trial of 3D Conformal Radiotherapy Versus Helical Tomotherapy IMRT in High-Risk Prostate Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
April 2020
Overall Recruitment Status
Unknown status
Study Start Date
March 2005 (undefined)
Primary Completion Date
January 2015 (Actual)
Study Completion Date
June 30, 2020 (Anticipated)

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
In this study we are comparing two forms of radiotherapy. This study is being done because it is not clear at present time whether intensity modulated radiotherapy (IMRT) can reduce side effects of radiotherapy compared to standard radiotherapy (called 3D-Conformal Radiotherapy).
Detailed Description
Radical radiation therapy plays an important role in the management of prostate cancer, yielding comparable long-term outcomes to surgery. Unfortunately, long term disease free survival data using PSA criteria have shown that less than 50% of high-risk patients are free of disease at 10 years. To improve on the results of conventional dose radiotherapy dose escalation with three-dimensional conformal radiation has been employed. Due to the irregular shape of the prostate and the variable motion of this organ there is substantial radiation of adjacent normal surrounding tissue during treatment which results in radiation-induced toxicity. Intensity-modulated radiation therapy (IMRT) is a new form of radiation therapy. Preliminary evidence suggests that IMRT improves the dose distribution during radiation therapy of the prostate. The hypothesis of this study is that IMRT delivered using Helical Tomotherapy can reduce late toxicity of radical radiotherapy as compared to three-dimensional conformal radiation (3DCRT) in high-risk prostate cancer patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer
Keywords
prostate, IMRT, tomotherapy, radiation, cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
72 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Arm A: 3D-Conformal Radiation
Arm Type
Other
Arm Description
Intervention: Standard radiation treatment for high risk prostate cancer. Once daily Monday to Friday for 8 weeks. 3DCRT 7800 cGY/39 Fractions/ STD Technique* Initial 4F 3DCRT to Nodes/ Prostate + Seminal Vesicles 4,600 cGy/23 Boost 6 F 3DCRT to Prostate 3,200 cGy/16
Arm Title
Arm B: Helical Tomotherapy Intensity Modulated Radiotherapy
Arm Type
Experimental
Arm Description
Intervention: Helical Tomotherapy Intensity Modulated Radiotherapy (IMRT) once daily Monday to Friday for 8 weeks. IMRT using Helical Tomotherapy* 7800 cGY/39 Fractions Boost IMRT to Prostate 3,200 cGy/16
Intervention Type
Radiation
Intervention Name(s)
Arm B: Helical Tomotherapy Intensity Modulated Radiotherapy
Other Intervention Name(s)
IMRT
Intervention Description
IMRT using Helical Tomotherapy* 7800 cGY/39 Fractions once daily Monday to Friday for 8 weeks Initial IMRT to Nodes/Prostate + Seminal Vesicles 4,600 cGy/23 Boost IMRT to Prostate 3,200 cGy/16
Intervention Type
Other
Intervention Name(s)
Arm A: 3D-Conformal Radiation
Other Intervention Name(s)
Radiation Therapy
Intervention Description
3DCRT 7800 cGY/39 Fractions/ STD Technique* once daily Monday to Friday for 8 weeks Initial 4F 3DCRT to Nodes/ Prostate + Seminal Vesicles 4,600 cGy/23 Boost 6 F 3DCRT to Prostate 3,200 cGy/16
Primary Outcome Measure Information:
Title
Late rectal toxicity from radiotherapy of the prostate
Description
Outcome measurements will be determined by physical exam and bloodwork.
Time Frame
Month 1, 4, 8, every 4 months during year 1-2, then every 6 months during years 2-5, then every 12 months until disease progression
Secondary Outcome Measure Information:
Title
Acute rectal toxicity, Acute and late bladder toxicity, Disease specific survival at 5 years, Biochemical relapse free survival at 5 years, Local control rates at 5 years, Quality of Life
Description
Outcome measurements will be determined by physical exam and bloodwork.
Time Frame
Month 1, 4, 8, every 4 months during year 1-2, then every 6 months during years 2-5, then every 12 months until disease progression

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: A pathologic diagnosis of adenocarcinoma of the prostate Age greater than 18 years ECOG performance status of 2 or less. Presence of any of the following high risk features: Clinical stage cT3-4 or Gleason score 8-10 or Pre-treatment PSA > 20ng/ml or Clinical N1/N2 or pathologic N1/N2 Exclusion Criteria: Patients with contraindication to radical radiation therapy including inflammatory bowel disease Prior or active malignancy except non-melanoma skin carcinoma within 5 years of the diagnosis of prostate cancer Prior pelvic radiotherapy for other malignancies Prior cytotoxic chemotherapy Prior orchiectomy, radical prostatectomy, cryotherapy or thermal ablation therapy for prostate cancer
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Shawn Malone, 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

Learn more about this trial

3D-Conformal Radiation vs Helical Tomotherapy in Prostate Cancer

We'll reach out to this number within 24 hrs