We plan to conduct a prospective, two-arm, open-label phase â…¡ study to evaluate whether transarterial chemoembolization with FOLFOX plus/minus intravenous cetuximab/bevacizumab significantly improves the efficacy and safety compared with systemic FOLFOX therapy plus/minus cetuximab/bevacizumab in elderly patients with advanced unresectable colorectal cancer.
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Objective Response Rateï¼›Disease Control Rate
Timeframe: 24 weeks