Preoperative Combined Radiation and Chemotherapy - Rectal Cancer
Primary Purpose
Rectal Neoplasms
Status
Completed
Phase
Phase 2
Locations
Canada
Study Type
Interventional
Intervention
Combined Radiation and Chemotherapy
Sponsored by
About this trial
This is an interventional treatment trial for Rectal Neoplasms
Eligibility Criteria
Inclusion Criteria: Biopsy proven adenocarcinoma of the rectum Performance status <2 (ECOG, appendix II) Clinical Stage T2 N1-2, T3-4 NO-2, without evidence of distant metastasis Exclusion Criteria: Prior pelvic irradiation Inflammatory bowel disease Evidence of distant metastasis Performance status >2
Sites / Locations
- University Health Network Princess Margaret Hospital
Outcomes
Primary Outcome Measures
Assess acute toxicity and complete remission rate of combined preoperative radiation and chemotherapy
Secondary Outcome Measures
Full Information
NCT ID
NCT00232453
First Posted
October 3, 2005
Last Updated
February 11, 2011
Sponsor
University Health Network, Toronto
Collaborators
Princess Margaret Hospital, Canada
1. Study Identification
Unique Protocol Identification Number
NCT00232453
Brief Title
Preoperative Combined Radiation and Chemotherapy - Rectal Cancer
Official Title
A Phase II Protocol of Preoperative Combined Radiation and Chemotherapy for Resectable Primary Rectal Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
February 2011
Overall Recruitment Status
Completed
Study Start Date
March 2001 (undefined)
Primary Completion Date
December 2004 (Actual)
Study Completion Date
December 2004 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
University Health Network, Toronto
Collaborators
Princess Margaret Hospital, Canada
4. Oversight
5. Study Description
Brief Summary
There is no established standard preoperative treatment in rectal cancer. Two large randomized studies in North America closed from lack of accrual; therefore the only method of assessing preoperative treatment in rectal cancer is from Phase II studies. This study builds on the experience at PMH gained in two previous studies which demonstrated a lower than expected toxicity with concurrent 5FU infusion and external radiotherapy. The current standard at PMH is preoperative radiation, 46Gy in 23 fractions with concurrent 5FU infusion 225mg/m2. An increase of radiation dose and consequent increase in chemotherapy may improve the response rate, but may also increase toxicity. It is proposed to increase the dose of radiotherapy to 50Gy in 25 fractions with concurrent chemotherapy and measure acute toxicity and complete remission rate.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rectal Neoplasms
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
34 (false)
8. Arms, Groups, and Interventions
Intervention Type
Procedure
Intervention Name(s)
Combined Radiation and Chemotherapy
Primary Outcome Measure Information:
Title
Assess acute toxicity and complete remission rate of combined preoperative radiation and chemotherapy
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Biopsy proven adenocarcinoma of the rectum
Performance status <2 (ECOG, appendix II)
Clinical Stage T2 N1-2, T3-4 NO-2, without evidence of distant metastasis
Exclusion Criteria:
Prior pelvic irradiation
Inflammatory bowel disease
Evidence of distant metastasis
Performance status >2
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
James Brierley, MD
Organizational Affiliation
Princess Margaret Hospital, Canada
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Health Network Princess Margaret Hospital
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G 2M9
Country
Canada
12. IPD Sharing Statement
Learn more about this trial
Preoperative Combined Radiation and Chemotherapy - Rectal Cancer
We'll reach out to this number within 24 hrs