Overview

Combination Chemotherapy and Radiation Therapy in Treating Patients With Colorectal Cancer

Status:
Completed
Trial end date:
2009-12-01
Target enrollment:
0
Participant gender:
All
Summary
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one drug and combining radiation therapy with chemotherapy may kill more tumor cells. PURPOSE: Phase I trial to study the effectiveness of combination chemotherapy consisting of fluorouracil-uracil and leucovorin plus radiation therapy in treating patients with colorectal cancer who have undergone surgery to remove the tumor.
Phase:
Phase 1
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Memorial Sloan Kettering Cancer Center
Treatments:
Calcium
Leucovorin
Levoleucovorin
Tegafur
Criteria
DISEASE CHARACTERISTICS: Diagnosis of colorectal cancer for which postoperative
radiotherapy to the pelvis is indicated

PATIENT CHARACTERISTICS: Age: 18 and over Performance status: ECOG 0-2 Life expectancy: At
least 3 months Hematopoietic: WBC at least 4,000/mm3 Absolute granulocyte count at least
1,500/mm3 Platelet count at least 100,000/mm3 Hepatic: Bilirubin no greater than 1.5 mg/dL
ALT no greater than 1.25 times upper limit of normal (ULN) (no greater than 5 times ULN if
elevation secondary to malignancy) Alkaline phosphatase no greater than 1.25 times ULN (no
greater than 5 times ULN if elevation secondary to malignancy) Renal: Creatinine normal OR
Creatinine clearance normal or greater than 60 mL/min Other: No medical or psychiatric
condition that would preclude study No prior malignancy except: Appropriately treated
localized epithelial skin or cervical cancer Remote history of other cured malignancy (at
the discretion of the sponsor) Not pregnant or nursing Negative pregnancy test Fertile
patients must use effective contraception

PRIOR CONCURRENT THERAPY: Biologic therapy: No concurrent antineoplastic biological
response modifiers Chemotherapy: No prior systemic chemotherapy Endocrine therapy: Not
specified Radiotherapy: See Disease Characteristics No prior radiotherapy to the pelvis
Surgery: See Disease Characteristics Other: No other concurrent investigational drugs No
other concurrent antineoplastic therapy No concurrent halogenated antiviral agent (e.g.,
sorivudine)