GTI-2040, Oxaliplatin, and Capecitabine in Treating Patients With Locally Advanced or Metastatic Colorectal Cancer or Other Solid Tumors

• Status: Completed
• Trial end date: 1969-12-31
• Target enrollment: 0
• Participant gender: All

Summary

This phase I trial is studying the side effects and best dose of capecitabine when given together with GTI-2040 and oxaliplatin in treating patients with locally advanced or metastatic colorectal cancer or other solid tumors. Drugs used in chemotherapy, such as oxaliplatin and capecitabine, work in different ways to stop tumor cells from dividing so they stop growing or die. GTI-2040 may increase the effectiveness of chemotherapy by making tumor cells more sensitive to the drugs. Giving GTI-2040 together with oxaliplatin and capecitabine may kill more tumor cells

• Phase: Phase 1
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: National Cancer Institute (NCI)
• Treatments: Capecitabine; Oxaliplatin

Criteria

Inclusion Criteria:

• Patients must have locally advanced or metastatic colorectal cancer that is not amenable to surgical treatment; selected patients with advanced disease in incurable cancers of other types may be considered

• Patients must have histological or cytological proof of malignancy

• Patients must have had at least one standard prior chemotherapy for locally advanced or metastatic disease with no prior oxaliplatin containing regimen; patients who relapse within 12 months of adjuvant therapy are eligible

• Karnofsky performance status of >= 60%

• Absolute neutrophil count > 1500/ul

• Platelets > 100,000/ul

• Total bilirubin within institutional normal limits

• AST (SGOT)/ALT (SGPT) within 2.5 x institutional normal limits

• Alkaline phosphatase within 2.5x institutional normal limits

• Creatinine within institutional normal limits or a calculated creatinine clearance > 60 ml/min

• Patients should have no greater than grade 1 neuropathy (CTCAE v3.0)

• Ability to understand and the willingness to sign a written IRB approved consent document

• Measurable disease not required

• Previous chemotherapy must have been completed > 21 days before treatment on this study (> 6 weeks for mitomycin-c or nitrosoureas)

• Life expectancy of at least 12 weeks

Exclusion Criteria:

• Active or chronic hepatitis B or C

• HIV positive patients receiving antiviral therapy because of possible pharmacokinetic interactions

• Uncontrolled intercurrent illnesses including but not limited to ongoing or active infections, symptomatic congestive heart failure, unstable angina, or cardiac arrhythmia

• Pregnant or nursing women are excluded due to the potential for teratogenic effects and for potential deleterious effects on the infant; woman of childbearing age and men must practice an effective form of contraception

• Patients with known brain metastasis are excluded due their poor prognosis and due to possible neurologic sequelae that could confound the evaluation of the investigational treatment

• Patients requiring anticoagulation are excluded as polyanions are known to inhibit clotting mechanisms and phosphorothioate oligonucleotide may act in a similar mechanism; patients receiving low dose prophylactic Coumadin (1 mg/day) may be included

• Medical, social, of psychological factors that would interfere with consent and follow-up

• Patients with a diagnosis of pulmonary fibrosis or a pulmonary interstitial process