About this trial
We plan to conduct a prospective, two-arm, open-label phase Ⅱ 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.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Age ≥ 65 years, gender not restricted Pathologically confirmed advanced colorectal cancer without the opportunity for curative surgery Karnofsky Performance Status (KPS) score ≥ 60, with an estimated survival time ≥ 3 months At least 1 measurable colorectal lesion No prior systemic chemotherapy, or a minimum interval of 6 months between the last chemotherapy and study enrollment Voluntary signing of the informed consent form
Disqualifiers
Concomitant other malignant tumors Presence of gastrointestinal perforation Severe cardiovascular and cerebrovascular diseases Patients with hypersensitivity to study drugs or psychiatric disorders
Trial design
Parallel
Treatments tested in this trial
Transarterial chemoembolization
Procedure/SurgeryTransarterial chemoembolization with FOLFOX plus/minus intravenous cetuximab/bevacizumab
Treatment groups
Trial outcomes
Primary outcomes
Objective Response Rate;Disease Control Rate
Locations
Sponsors and contacts
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Junpeng Wang
Lead sponsor
Guang'anmen Hospital of China Academy of Chinese Medical Sciences
Sponsor institution
Peking Union Medical College Hospital
Collaborator
This trial is not recruiting at the moment. You can still explore other options: