Metastatic Colorectal Cancer
Conditions
Keywords
metastatic colorectal cancer, mCRC, ERCC-1, ERCC1, AGMT
Brief summary
This pilot study is being mounted to assess whether treatment assignment by ERCC-1 gene expression status suggests better clinical results from historical experience in metastatic colorectal cancer (mCRC). In wild type KRAS mCRC patients treated with either FOLFOX or FOLFIRI in combination with cetuximab the median response rate is approximately 60-65%. Biomarker directed treatment in this study may demonstrate that patients with low ERCC-1 treated with FOLFOX and cetuximab, and those with high ERCC-1 treated with FOLFIRI and cetuximab, will improve response rate to 70-75%. KRAS wild type patients will be treated with 6 cycles of one of the following regimens chosen for optimization based on patient characteristics (primary treatment phase). Patients with ERCC-1 \< 1.7 relative gene expression of ERCC-1 over ß-actin (ERCC-1 low) will be assigned to treatment with mFOLFOX6 in combination with Cetuximab. Patients with ERCC-1 gene expression \> 1.7 relative gene expression of ERCC-1 over over ß-actin (ERCC-1 high) will be assigned to treatment with FOLFIRI in combination with Cetuximab.
Interventions
DRUGmodifiedFOLFOX6 + Cetuximab
Sponsors
Merck Sharp & Dohme LLC
Arbeitsgemeinschaft medikamentoese Tumortherapie
Study design
Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
1.1 Inclusion criteria for pre-screening phase: * Untreated advanced metastatic colorectal cancer patients * Adequate tissue to evaluate for genotyping (10 x 10µm thick formalin fixed paraffin embedded tissue sections and one corresponding HE stained slide or a FFPE tumor block) 1.2 Inclusion criteria for treatment phase: Patients must fulfill all criteria listed below prior to enrolment in the study: * Untreated wild-type KRAS metastatic colorectal cancer * Previous adjuvant therapy must have been completed \> 6 months before therapy initiation on this study * Age \>18 years * Measureable disease with CT or MRI * ECOG performance status of 0-2 * Adequate organ function * Hematologic: * Absolute neutrophil count \> 1,500/µL * Hemoglobin \>9 mg/dl * Platelet count \>100,000 /µl * Renal: * Serum creatinine \<1.5 x Upper limit of normal (UPN) or estimated clearance \> 30 ml/min * Hepatic: * Serum bilirubin \< 1.5 mg/dl
Exclusion criteria
* Creatinine clearance below 30 ml/min * Patients with a history of other malignancies within 2 years prior to study entry, except for adequately treated carcinoma in situ of the cervix; basal or squamous cell skin cancer; low grade, early stage localized prostate cancer treated surgically with curative intent; good prognosis DCIS of the breast treated with lumpectomy alone with curative intent. * Patients with a history of severe cardiac disease; e.g. NYHA Functional Class III or IV heart failure, myocardial infarction within 6 months, ventricular tachyarrhythmias requiring ongoing treatment, or unstable angina. * Other known co-morbidity with the potential to dominate survival * Hypersensitivity with anaphylactic reaction to humanized monoclonal antibodies or any of the applied drugs * Pregnant or breast feeding women * Any co-existing medical or psychological condition that would preclude participation in the study or compromise ability to give informed consent.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Response | 5 years | Treatment response according to Response Evaluation Criteria In Solid Tumors \[RECIST\] |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Response rate | 5 years | Description of group differences between ERCC-1 low and ERCC-1 high patients with respect to response rate, PFS and OS |
| Patient characteristics | 5 years | Description of group differences between ERCC-1 low and ERCC-1 high patients with respect to KRAS status |
| Progression free survival (PFS) | 5 years | — |
| Molecular markers for toxicity | 5 years | — |
| Number of adverse events during study treatment | 5 years | — |
| Secondary resection rate | 5 years | — |
Countries
Austria
Outcome results
None listed