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Radiation Therapy With Capecitabine in Rectal Cancer

Primary Purpose

Rectal Cancer

Status
Terminated
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Capecitabine
Radiation
Surgery
Sponsored by
University of Michigan Rogel Cancer Center
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Rectal Cancer

Eligibility Criteria

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

Eligibility Criteria Histologic confirmation of adenocarcinoma of the rectum. The lesion must be located in the rectum. For purposes of this study, the lesion must be within 12 cm of the anus as measured by sigmoidoscopy. Patients must have indication of a locally advanced lesion defined for this study as tumor through the bowel wall (> T3) or involving regional lymph nodes (>N1). Clinical stage determination may be made by physical examination (for T4 lesions only), endoscopic ultrasound or CT scan of pelvis. Patients with metastatic disease are eligible provided operative intervention on primary site is anticipated. Patients must have adequate organ function defined as pretreatment leukocyte count > 3,000/ul, platelet count > 100,000/ul, serum creatinine < 2.0 mg/dl, serum bilirubin < 2 mg/dl. Note: Capecitabine is contraindicated in patients with severe renal impairment (creatinine clearance < 30 ml/min). In patients with calculated creatinine clearance of 30-50 ml/min capecitabine will begin at (-)1 level dose reduction (see section 6.3) Patients must be at least 18 years of age and have a Zubrod performance status of < 2 (see appendix 1.) Patients must be informed of the investigational nature of this study and provide written informed consent in accordance with institutional and federal guidelines prior to the initiation of therapy. Exclusion Criteria: Patients may not have received previous pelvic irradiation for any indication, or previous chemotherapy for cancer therapy within the preceding 6 months. Patients must have no other serious medical or psychiatric illness that would limit the ability of the patient to receive protocol therapy or provide informed consent. Pregnant or lactating women may not participate. Women/men of reproductive potential must agree to use an effective contraceptive method. Patients with lack of physical integrity of the upper gastrointestinal tract, inability to swallow tablets or those who have malabsorption syndrome are not eligible.

Sites / Locations

  • University of Michigan Cancer Center

Outcomes

Primary Outcome Measures

Objectives:
In patients with locally advanced rectal cancer treated with preoperative radiation and capecitabine chemotherapy to estimate:
a. the pathologic complete response rate
b. the clinical response rate
c. the proportion of patients converted to sphincter sparing surgery
clinical response rate
d. The quantitative and qualitative toxicities of the treatment approach
e. The relationship of intratumoral levels of thymidylate synthase, dipyrimidine dehydrogenase and thymidine phosphorylase determined immunohistochemically to response

Secondary Outcome Measures

Full Information

First Posted
September 12, 2005
Last Updated
December 28, 2007
Sponsor
University of Michigan Rogel Cancer Center
Collaborators
Hoffmann-La Roche
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1. Study Identification

Unique Protocol Identification Number
NCT00176787
Brief Title
Radiation Therapy With Capecitabine in Rectal Cancer
Official Title
Phase II Trial of Preoperative Radiation Therapy With Capecitabine in Rectal Cancer (UMCC 0046)
Study Type
Interventional

2. Study Status

Record Verification Date
December 2007
Overall Recruitment Status
Terminated
Why Stopped
recruitment goals met
Study Start Date
October 2000 (undefined)
Primary Completion Date
May 2005 (Actual)
Study Completion Date
June 2007 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
University of Michigan Rogel Cancer Center
Collaborators
Hoffmann-La Roche

4. Oversight

5. Study Description

Brief Summary
This study will use an experimental combination of treatment with the drug Capecitabine and radiation therapy prior to an operation for removal of the patient's tumor. The drug Capecitabine is an oral form of a drug called 5-FU which has been widely used to treat rectal cancer. This is a phase II clinical trial, which means that the physician will be studying the reactions of the patient's body and tumor to treatment with Capecitabine and radiation therapy. The purpose of this study is to see if the tumor responds to this treatment and to determine how long the response lasts. The study also will see what kind of side effects this experimental treatment causes and see how often these side effects occur. Preliminary human studies using Capecitabine and radiation therapy have produced encouraging results with acceptable side effects.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Rectal Cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
30 (false)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Capecitabine
Intervention Type
Procedure
Intervention Name(s)
Radiation
Intervention Type
Procedure
Intervention Name(s)
Surgery
Primary Outcome Measure Information:
Title
Objectives:
Title
In patients with locally advanced rectal cancer treated with preoperative radiation and capecitabine chemotherapy to estimate:
Title
a. the pathologic complete response rate
Title
b. the clinical response rate
Title
c. the proportion of patients converted to sphincter sparing surgery
Title
clinical response rate
Time Frame
2 cycles
Title
d. The quantitative and qualitative toxicities of the treatment approach
Title
e. The relationship of intratumoral levels of thymidylate synthase, dipyrimidine dehydrogenase and thymidine phosphorylase determined immunohistochemically to response

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Eligibility Criteria Histologic confirmation of adenocarcinoma of the rectum. The lesion must be located in the rectum. For purposes of this study, the lesion must be within 12 cm of the anus as measured by sigmoidoscopy. Patients must have indication of a locally advanced lesion defined for this study as tumor through the bowel wall (> T3) or involving regional lymph nodes (>N1). Clinical stage determination may be made by physical examination (for T4 lesions only), endoscopic ultrasound or CT scan of pelvis. Patients with metastatic disease are eligible provided operative intervention on primary site is anticipated. Patients must have adequate organ function defined as pretreatment leukocyte count > 3,000/ul, platelet count > 100,000/ul, serum creatinine < 2.0 mg/dl, serum bilirubin < 2 mg/dl. Note: Capecitabine is contraindicated in patients with severe renal impairment (creatinine clearance < 30 ml/min). In patients with calculated creatinine clearance of 30-50 ml/min capecitabine will begin at (-)1 level dose reduction (see section 6.3) Patients must be at least 18 years of age and have a Zubrod performance status of < 2 (see appendix 1.) Patients must be informed of the investigational nature of this study and provide written informed consent in accordance with institutional and federal guidelines prior to the initiation of therapy. Exclusion Criteria: Patients may not have received previous pelvic irradiation for any indication, or previous chemotherapy for cancer therapy within the preceding 6 months. Patients must have no other serious medical or psychiatric illness that would limit the ability of the patient to receive protocol therapy or provide informed consent. Pregnant or lactating women may not participate. Women/men of reproductive potential must agree to use an effective contraceptive method. Patients with lack of physical integrity of the upper gastrointestinal tract, inability to swallow tablets or those who have malabsorption syndrome are not eligible.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mark Zalupski, M.D.
Organizational Affiliation
University of Michigan Rogel Cancer Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Michigan Cancer Center
City
Ann Arbor
State/Province
Michigan
ZIP/Postal Code
48109
Country
United States

12. IPD Sharing Statement

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Radiation Therapy With Capecitabine in Rectal Cancer

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