Rectal Cancer Clinical Trial
Official title:
Phase II Study of Cetuximab, 5-FU and Radiation as Neoadjuvant Therapy for Patients With Locally Advanced Rectal Cancer
The standard treatment for rectal cancer is to receive the chemotherapeutic drug 5-fluorouracil (5-FU) with radiation therapy before having surgery to remove the rectal cancer. This is known as neoadjuvant chemoradiotherapy. The purpose of this research study is to determine if Cetuximab improves the benefits of neoadjuvant chemoradiotherapy when given with 5-FU and radiation therapy.
The epidermal growth factor receptor (EGFR) present in normal and tumor cells is involved in
signaling pathways affecting cellular growth, differentiation, proliferation and programmed
cell death. Overexpression of EGFR has been associated with poorer prognosis in colorectal
cancer. Cetuximab targets and blocks EGFR and has been shown to be safe and effective in
treating colorectal cancer and head and neck cancers.
The primary hypothesis is that cetuximab in combination with standard 5-FU and radiation as
neoadjuvant therapy would improve pathological complete response (pCR) compared to the
historical rate (30% versus 10%). The regimen would be considered promising if 5 or more of
25 evaluable participants achieve pCR. The probability of observing this outcome is 0.91 and
0.10 if the true pCR rate is 30% and 10%, respectively.
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