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NCCTG NO147
Principal Investigator: Peter Kozuch, MD
Time frame of study: Ongoing
Location of Study:

Beth Israel Medical Center
St.Luke's-Roosevelt Hospital Center

Contact:

Continuum Cancer Research Program
(212) 844-6286

 

Summary:
The chemotherapy regimen 5-fluorouracil/leucovorin and oxaliplatin has been established as the current standard of care for adjuvant treatment of colon cancer.

The antibody cetuximab is directed against the epidermal growth factor receptor (EGFR), which is involved in the development and progression of many common tumors including colon cancer. Cetuximab has demonstrated a survival benefit in metastatic colon cancer (cancer that has spread to other organs). This trial will compare the disease free survival benefit and side effects of 5-fluorouracil and oxaliplatin with or without additional cetuximab.

Eligibility and Treatment Plan:
Patients, 18 years and older, with histologically confirmed adenocarcinoma of the colon (Stage III tumor completely resected), at least 1 pathologically confirmed lymph node identified, and no residual lymph node disease.

There are two treatment arms: (one cycle of therapy is a 2-week treatment period)
• Arm A) 12 cycles of oxaliplatin, 5-fluourouracil, and leucovorin,
• Arm D) 12 cycles of cetuximab + oxaliplatin, 5-fluourouracil, and leucovorin. Treatment will be intravenous (through the vein).

Benefits and/or Compensation:
Participants receive study-related medication at no charge under the supervision and care of a team of medical professionals. The information gathered from this study may be beneficial to future patients, and cetuximab may improve disease free and overall survival time for stage III colon cancer patients.