Colorectal Cancer
Conditions
Keywords
recurrent colon cancer, stage IV colon cancer, recurrent rectal cancer, stage IV rectal cancer
Brief summary
RATIONALE: Studying samples of blood and tumor tissue in the laboratory from patients with cancer receiving chemotherapy may help doctors understand the effect of chemotherapy on biomarkers. It may also help doctors predict how patients will respond to treatment. PURPOSE: This phase IV trial is studying biomarkers in patients undergoing chemotherapy for metastatic colorectal cancer.
Detailed description
OBJECTIVES: Primary * Research the oncogenetic parameters and pharmacogenetic and pharmacokinetic predictors of therapeutic response and toxic effects. Secondary * Study the correlations between the pharmacogenetic and pharmacokinetic parameters. * Study the predictive value of these parameters on disease-free and overall survival. OUTLINE: This is a multicenter study. Patients receive 1 of 4 chemotherapy regimens: * Regimen 1: Fluorouracil and leucovorin calcium * Regimen 2: Capecitabine and leucovorin calcium * Regimen 3: Irinotecan hydrochloride * Regimen 4: Oxaliplatin Tumor and blood samples are collected before the start of chemotherapy and are examined by pharmacogenetic analysis. Clinical and biological parameters are also studied. Blood samples are also collected during the first course of chemotherapy for pharmacokinetic studies. After completion of study therapy, patients are followed periodically for 3 years.
Interventions
DRUGirinotecan hydrochloride
DRUGcapecitabine
DRUGfluorouracil
DRUGleucovorin calcium
DRUGoxaliplatin
OTHERlaboratory biomarker analysis
OTHERpharmacological study
Sponsors
Centre Hospital Regional Universitaire de Limoges
Study design
Allocation
NON_RANDOMIZED
Primary purpose
TREATMENT
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
DISEASE CHARACTERISTICS: * Histologically confirmed metastatic colorectal cancer * Unresectable metastatic disease must be confirmed histologically if \> 2 years since primary diagnosis * Measurable metastatic disease \> 1 cm by spiral CT scan or \> 2 cm by other methods * Scheduled to receive first-line chemotherapy for metastatic disease * Chemotherapy must include fluorouracil, capecitabine, irinotecan hydrochloride, or oxaliplatin * No inadequate or unusable tissue as the only tissue available * No known brain metastases or meningeal disease PATIENT CHARACTERISTICS: * WHO performance status 0-2 * No contraindication to chemotherapy * Not pregnant or nursing * Fertile patients must use effective contraception * No other severe pathology that is likely to worsen during therapy * No dementia or severely impaired mental condition * No geographical or psychological reasons that would preclude treatment PRIOR CONCURRENT THERAPY: * See Disease Characteristics * No prior therapy for metastatic cancer * Prior adjuvant chemotherapy allowed * Concurrent bevacizumab or other monoclonal antibody therapy allowed
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Oncogenetic parameters | — |
| Pharmacogenetic and pharmacokinetic predictors of therapeutic response and toxic effects | — |
Secondary
| Measure | Time frame |
|---|---|
| Correlations between the pharmacogenetic and pharmacokinetic parameters | — |
| Predictive value of pharmacogenetic and pharmacokinetic parameters on disease-free and overall survival | — |
Countries
France
Outcome results
None listed