Cadonilimab Combined With Fruquintinib and SBRT as Athird-line and Posterior Line Treatment in Patients With MSS CRC

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-75
SponsorLiu Huang

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

80 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Liu Huang

Lead sponsor

Tongji Hospital

Sponsor institution