Colorectal Cancer Clinical Trial
Official title:
Phase II Study of Recurrent Ganglionic Colorectal Cancer Not Accessible By Surgery Treated Using Chemotherapy With Simplified FOLFOX7 Followed By Radiotherapy Combined With 5FU and Oxaliplatin
RATIONALE: Drugs used in chemotherapy, such as oxaliplatin, fluorouracil, and leucovorin,
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 more than one drug (combination chemotherapy) together with radiation therapy may
kill more tumor cells.
PURPOSE: This phase II trial is studying how well giving combination chemotherapy together
with radiation therapy works in treating patients with recurrent metastatic colorectal
cancer.
OBJECTIVES:
Primary
- Determine the response rate in patients with recurrent metastatic colorectal cancer
treated with neoadjuvant oxaliplatin, fluorouracil, and leucovorin calcium followed by
radiotherapy and concurrent fluorouracil and oxaliplatin.
Secondary
- Determine the overall survival and disease-free survival of patients treated with this
regimen.
- Determine the primary site of recurrence and time to recurrence in patients treated
with this regimen.
- Determine quality of life of patients treated with this regimen.
OUTLINE: This is a nonrandomized, open-label, multicenter study.
- Neoadjuvant chemotherapy: Patients receive oxaliplatin IV over 2 hours and leucovorin
calcium IV over 2 hours on day 1. Patients also receive fluorouracil IV continuously
over 46 hours beginning day 1. Treatment repeats every 14 days for 4 courses in the
absence of disease progression or unacceptable toxicity. Two to 5 weeks later, patients
with stable or responding disease proceed to chemoradiotherapy.
- Chemoradiotherapy: Patients receive fluorouracil IV continuously 5 days a week for 5
weeks and oxaliplatin IV over 1 hour on days 1, 8, 15, 22, and 29. Patients also
undergo radiotherapy 5 days a week for 5 weeks beginning on day 1.
Quality of life is assessed at baseline, 1 week after the completion of neoadjuvant
chemotherapy, on days 15, 30, and 42 of chemoradiotherapy, and at 1 and 2 months after the
completion of study treatment.
After completion of study treatment, patients are followed periodically.
PROJECTED ACCRUAL: A total of 39 patients will be accrued for this study.
;
Allocation: Non-Randomized, Masking: Open Label, Primary Purpose: Treatment
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