Viewing Study NCT00002593



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Last Modification Date: 2024-10-26 @ 9:03 AM
Study NCT ID: NCT00002593
Status: COMPLETED
Last Update Posted: 2013-01-03
First Post: 1999-11-01

Brief Title: S9415 Chemotherapy in Patients With Stage II or III Colon Cancer That Has Been Surgically Removed
Sponsor: SWOG Cancer Research Network
Organization: SWOG Cancer Research Network

Study Overview

Official Title: Phase III Randomized Trial of 5-FULeucovorinLevamisole Versus 5-FU Continuous InfusionLevamisole as Adjuvant Therapy for High-Risk Resectable Colon Cancer
Status: COMPLETED
Status Verified Date: 2013-01
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief 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 giving drugs in different ways may kill more cancer cells

PURPOSE Randomized phase III trial to compare the effectiveness of chemotherapy given in different ways in treating patients with surgically removed stage II or stage III colon cancer at high risk of recurrence
Detailed Description: OBJECTIVES I Compare overall and disease free survival in patients with completely resected stage II or III colon cancer randomized to adjuvant chemotherapy with bolus fluorouracil and leucovorin calcium with levamisole vs continuous infusion fluorouracil with levamisole

OUTLINE This is a randomized multicenter study Patients are stratified according to center T stage T1 vs T2 vs T3 vs T4a N stage N0 vs N1 vs N2-3 and time from surgery until registration 21-28 vs 29-35 days Patients are randomized to one of two treatment arms Arm I Patients receive leucovorin calcium IV immediately followed by fluorouracil IV on days 1 through 5 of weeks 1 5 9 14 19 and 24 and oral levamisole 3 times a day for 3 days on days 1-3 Courses repeat every 2 weeks for 6 months Arm II Patients receive levamisole as in arm I plus fluorouracil by continuous IV infusion for 8 weeks Treatment with fluorouracil repeats every 10 weeks for 3 courses Treatment continues in the absence of disease progression or unacceptable toxicity Patients are followed at 9 months and 12 months then every 6 months for 4 years and then annually thereafter

PROJECTED ACCRUAL A total of 1500 patients will be accrued for the study over approximately 55 years

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
SWOG-9415 OTHER None None
CLB-9498 OTHER None None
INT-0153 OTHER None None
U10CA032102 NIH NCI httpsreporternihgovquickSearchU10CA032102