SBRT Combined With Fruquintinib Plus PD-1/CTLA-4 Antibody for Third-line Treatment in mCRC

The study is a phase II clinical study. The purpose of the study is to evaluate the efficacy and safety of SBRT combined with Fruquintinib Plus PD-1/CTLA-4 Antibody for Third-line Treatment in mCRC.

Inclusion Criteria:Patients must have biopsy proven unresectable MCRC.Patients must have received first-line and second-line chemotherapy, and approved a progressive disease.Age ≥ 18 yearsPatients must have measurable disease at baseline.Patients can have up to only 5 discrete active extracranial lesions (≤3 in the liver and ≤3 in the lung) identified by position-emission tomography (PET) scan and also seen on correlative plain film, CT scan, or MRI within 8 weeks prior to the initiation of radiotherapy.Patients who previously received radiotherapy to the primary site will be ineligible if there is CT evidence of disease progression within the past 3 months.Patients must have a Karnofsky Performance Scores (KPS) >60 8. Aspartate aminotransferase, alanine aminotransferase & Alkaline phosphates must be ≤ 2.5 times the upper limit of normal (ULN). Total bilirubin must be within the limit of normal.9. Patients should have adequate bone marrow function as defined by peripheral granulocyte count of ≥1500/mm3. 10. Patients should have adequate renal function (serum creatinine ≤1.5 times the ULN). 11. Females of childbearing potential should have a negative pregnancy test. 12. Patients who would be receiving radiation for lung lesions who are known or suspected by the treating radiation oncologist to have compromised lung function must have a documented forced expiratory volume in 1 second (FEV1) ≥ 1 litre.13. Patients must provide verbal and written informed consent to participate in the study.14. Total bilirubin: within normal institutional limitsExclusion Criteria:Patients with either untreated brain metastases or brain metastases treated within the past three months are ineligiblePatients with serious, uncontrolled, concurrent infection(s).Significant weight loss (>10%) in the prior 3 months.Treatment for other carcinomas within the last five years, except cured non-melanoma skin and treated in-situ cancers.Patients with more than 5 discrete metastatic lesions.Participation in any investigational drug study within 4 weeks preceding the start of study treatment.Unwillingness to participate or inability to comply with the protocol for the duration of the study.Patients who are pregnant. Patients with reproductive capability will need to use adequate contraception during the time of participation in the study