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Fluorouracil, Leucovorin, and Irinotecan in Treating Patients With Recurrent or Refractory Metastatic Unresectable Colorectal Cancer

Phase II Study of 5FU/Folinic Acid and Irinotecan as Second or Third Line Treatment in Patients With Metastatic, Unresectable, Colorectal Cancer

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00075595
Enrollment
Unknown
Registered
2004-01-12
Start date
2002-06-30
Completion date
Unknown
Last updated
2009-01-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal Cancer

Keywords

stage IV colon cancer, stage IV rectal cancer, recurrent colon cancer, recurrent rectal cancer, adenocarcinoma of the colon, adenocarcinoma of the rectum

Brief summary

RATIONALE: Drugs used in chemotherapy, such as fluorouracil, leucovorin, and irinotecan, use different ways to stop tumor cells from dividing so they stop growing or die. Giving more than one chemotherapy drug may kill more tumor cells. PURPOSE: This phase II trial is studying how well giving fluorouracil together with leucovorin and irinotecan works in treating patients with recurrent or refractory metastatic unresectable colorectal cancer.

Detailed description

OBJECTIVES: Primary * Determine the time to progression and time to death from progression in patients with recurrent or refractory metastatic unresectable colorectal cancer treated with fluorouracil, leucovorin calcium, and irinotecan. Secondary * Determine the objective response and stabilization rate in patients treated with this regimen. * Determine the time to treatment failure in patients treated with this regimen. * Determine the duration of response in patients treated with this regimen. * Determine overall survival rate in patients treated with this regimen. * Determine the incidence of grade 3 or 4 toxicity in patients treated with this regimen. OUTLINE: This is an open-label, multicenter study. Patients receive leucovorin calcium IV over 2 hours on day 1, irinotecan IV over 1 hour on days 1 and 3, and fluorouracil IV continuously over 46 hours beginning on day 1. Courses repeat every 2 weeks in the absence of disease progression or unacceptable toxicity. Patients are followed every 3 months. PROJECTED ACCRUAL: A total of 78 patients will be accrued for this study within 18 months.

Interventions

DRUGFOLFIRI regimen
DRUGfluorouracil
DRUGirinotecan hydrochloride
DRUGleucovorin calcium

Sponsors

GERCOR - Multidisciplinary Oncology Cooperative Group
Lead SponsorOTHER

Study design

Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

DISEASE CHARACTERISTICS: * Histologically confirmed colorectal adenocarcinoma * Metastatic, unresectable disease * Meets 1 of the following criteria: * At least 1 unidimensionally measurable metastatic lesion at least 10 mm by spiral scan OR 20 mm by conventional scan * Evaluable disease * Evidence of disease (e.g., ascites or bone metastases) by imaging techniques * Progressive disease as defined by 1 of the following criteria: * Progressive disease while receiving first-line chemotherapy * Recurrent disease within 6 months after completing adjuvant chemotherapy * No symptomatic brain metastases PATIENT CHARACTERISTICS: Age * 18 to 80 Performance status * WHO 0-2 Life expectancy * At least 3 months Hematopoietic * Absolute neutrophil count ≥ 1,500/mm\^3 * Platelet count ≥ 100,000/mm\^3 Hepatic * Bilirubin \< 1.5 times upper limit of normal (ULN) * Alkaline phosphatase \< 3 times ULN Renal * Not specified Cardiovascular * No uncontrolled angina * No myocardial infarction within the past 6 months Gastrointestinal * No chronic diarrhea grade 2 or greater * No unresolved fully or partially obstructed intestine Other * Not pregnant or nursing * Fertile patients must use effective contraception * No other underlying disease or medical condition that would preclude study participation * No other prior malignancy except curatively treated basal cell cancer or carcinoma in situ of the cervix * No psychological, social, familial, or geographical condition that would preclude study follow-up PRIOR CONCURRENT THERAPY: Biologic therapy * Not specified Chemotherapy * See Disease Characteristics * No prior irinotecan Endocrine therapy * Not specified Radiotherapy * At least 3 weeks since prior radiotherapy Surgery * At least 3 weeks since prior surgery Other * No other concurrent clinical trial participation

Design outcomes

Primary

MeasureTime frame
Time to progression
Time to death from progression

Secondary

MeasureTime frame
Time to treatment failure
Duration of response
Objective response
Incidence of grade 3 or 4 toxicity
Overall survival rate
Stabilization rate

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026