Overview
Fluorouracil-Uracil and Leucovorin in Treating Elderly Patients With Metastatic Colorectal Cancer
Status:
Completed
Completed
Trial end date:
1969-12-31
1969-12-31
Target enrollment:
0
0
Participant gender:
All
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 may kill more tumor cells. PURPOSE: Phase II trial to study the effectiveness of fluorouracil-uracil and leucovorin in treating elderly patients who have metastatic colorectal cancer.Phase:
Phase 2Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Eastern Cooperative Oncology GroupCollaborator:
National Cancer Institute (NCI)Treatments:
Calcium
Leucovorin
Levoleucovorin
Tegafur
Criteria
DISEASE CHARACTERISTICS: Histologically confirmed metastatic colorectal adenocarcinomaMeasurable disease
PATIENT CHARACTERISTICS: Age: 75 and over Performance status: ECOG 0-2 Life expectancy: Not
specified Hematopoietic: Absolute neutrophil count at least 1,500/mm3 Platelet count at
least 100,000/mm3 Hepatic: Bilirubin no greater than 1.5 mg/dL AST or ALT no greater than
2.5 times upper limit of normal (ULN) Renal: Creatinine no greater than 1.5 times ULN
Other: No serious infection No other serious underlying medical condition that would
preclude protocol therapy No known hypersensitivity to fluorouracil-uracil or leucovorin
calcium
PRIOR CONCURRENT THERAPY: Biologic therapy: At least 6 months since prior adjuvant
immunotherapy for colorectal cancer No concurrent immunotherapy Chemotherapy: At least 6
months since prior adjuvant chemotherapy for colorectal cancer No other concurrent
chemotherapy Endocrine therapy: No concurrent hormonal therapy Radiotherapy: See Disease
Characteristics At least 6 months since prior adjuvant radiotherapy for colorectal cancer
Prior radiotherapy for locally symptomatic disease allowed Surgery: Prior surgery allowed
Other: No prior therapy for metastatic disease No other concurrent investigational drugs No
concurrent halogenated antiviral agents (e.g., lodenosine, fialuridine, FMAU,
emtricitabine, and sorivudine)