About this trial
An assessment of 6-month progression-free survival in patients with mCRC with third-line and postline metastatic colorectal cancer in combination with cardonilizumab and fuquinitinib and SBRT compared with fuquinitinib monotherapy
Eligibility criteria
Qualifiers
Age = 18 years, $75 years
Histologically or cytologically confirmed advanced Stage IV primary colorectal cancer
MSI status: MSS
At least two or more standard systemic therapies prior treatment (based on Fu, oxaliplatin, irinotecan, bevacizumab and cetuximab) of cytotoxic chemotherapy, treatment failure or intolerable toxicities
Disqualifiers
• Patients have received anti-PD-1 / PD-L1 or anti-CTLA-4 immunotherapy or other immunexperimental drugs
Patients with severe autoimmune diseases: active inflammatory bowel disease (including Cohn's disease and ulcerative colitis), rheumatoid arthritis, scleroderma, systemic lupus ervthematosus, autoimmune vasculitis (such as Wegener's granuloma), etc
Symptomatic interstitial lung disease or active infection/non-infectious pneumonia
Risk factors of intestinal perforation: active diverticulitis, abdominal abscess, gastrointestinal obstruction, abdominal cancer or other known risk factors of intestinal perforation
Trial design
Treatments tested in this trial
- Fruquintinib
- Cadonilimab
- SBRT
Treatment groups
Sponsors and collaborators
Liu Huang
Lead sponsor
Tongji Hospital
Sponsor institution