Bortezomib, Fluorouracil, and External-Beam Radiation Therapy in Treating Patients With Stage II, Stage III, or Stage IV Rectal Cancer
- Conditions
- Colorectal Cancer
- Registration Number
- NCT00280176
- Lead Sponsor
- UNC Lineberger Comprehensive Cancer Center
- Brief Summary
RATIONALE: Bortezomib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor. Drugs used in chemotherapy, such as fluorouracil, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Radiation therapy uses high-energy x-rays to kill tumor cells. Giving bortezomib and fluorouracil together with radiation therapy may kill more tumor cells.
PURPOSE: This phase I trial is studying the side effects and best dose of bortezomib when given together with fluorouracil and external-beam radiation therapy in treating patients with stage II, stage III, or stage IV rectal cancer.
- Detailed Description
OBJECTIVES:
Primary
* Determine the maximum tolerated dose of bortezomib when administered in combination with fluorouracil and external beam radiotherapy as preoperative or palliative treatment in patients with stage II-IV rectal adenocarcinoma.
* Determine the dose-limiting toxicities of this regimen in these patients.
Secondary
* Determine the dose-effect relationship of bortezomib on NF-kappa B activation induced by chemoradiotherapy.
* Determine downstream events induced by NF-kappa B activation.
* Determine downstream events related to activation of p53 in response to treatment with chemoradiotherapy and bortezomib.
* Determine the rate of complete pathologic remission in patients who undergo surgical resection of their primary tumor.
* Determine the gene expression pattern of tumors by cDNA microarray analysis before and during treatment with this regimen.
OUTLINE: This is a multicenter, dose-escalation study of bortezomib.
Patients receive bortezomib IV on days 1, 4, 8, 11, 22, 25, 29, and 32 and fluorouracil IV continuously on days 2-38. Patients also undergo external beam radiotherapy 5 days a week for 5½ weeks. Treatment continues in the absence of disease progression or unacceptable toxicity.
Cohorts of 3-6 patients receive escalating doses of bortezomib until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose-limiting toxicity.
Patients undergo tissue biopsy at baseline and on days 1 and 2. Samples are collected and evaluated by tissue microarray analysis for NF-kappa B pathway activation; cDNA analysis, RNase protection assay, and immunohistochemistry for analysis of downstream events induced by NF-kappa B activation; and modified TdT-mediated dUTP nick-end label for analysis of apoptosis by DNA fragmentation. NF-kappa B subunits are quantified by enzyme-linked immunosorbent assay. Serum samples are collected at baseline and stored for future studies.
After completion of study treatment, patients are followed every 3 months for up to 2 years.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 11
Not provided
Not provided
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Primary Outcome Measures
Name Time Method Maximum tolerated dose 6 weeks Dose-limiting toxicity 8 weeks
- Secondary Outcome Measures
Name Time Method Dose-effect relationship of bortezomib on NF-kappa B activation induced by chemoradiotherapy 6 weeks Downstream events induced by NF-kappa B activation 8 weeks Downstream events related to activation of p53 in response to treatment with chemoradiotherapy and bortezomib 8 weeks Rate of complete pathologic remission 2 years Gene expression pattern of tumors as assessed by cDNA microarray analysis pre- and post-treatment 8 weeks
Trial Locations
- Locations (2)
Vanderbilt-Ingram Cancer Center
🇺🇸Nashville, Tennessee, United States
Lineberger Comprehensive Cancer Center at University of North Carolina - Chapel Hill
🇺🇸Chapel Hill, North Carolina, United States