FOLFOX-HAIC as Conversion Treatment for Initially Unresectable Colorectal Liver Metastasis

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-75
SponsorTongji Hospital

About this trial

Try FOLFOX-HAIC combining bevacizumab or cetuximab for initially unresectable colorectal liver metastasis patients to increase the conversion to resection rate to improve long-term survival outcomes

Eligibility criteria

Qualifiers

age 18-75 years

no history of other malignant diseases

refuse or progress in prior systemic treatment

diagnosed as CRLM confirmed by pathology, in spite of whether the primary tumor had been resected

Disqualifiers

extra-hepatic metastasis verified by medical imaging

unable to tolerate chemotherapy, anesthesia or surgery

allergy or previous intolerable to any agent of oxaliplatin, leucovorin, 5-Fu, bevacizumab or cetuximab

tumor spread in abdomen

Trial design

Treatments tested in this trial

  • FOLFOX (oxaliplatin, leucovorin, 5-fluorouracil [5FU])
  • hepatic arterial infusion chemotherapy (HAIC)
  • Bevacizumab
  • Cetuximab (Erbitux)
  • liver resection

Treatment groups

300 Participants
are divided into 1 treatment group

Sponsors and collaborators