To explore the efficacy and safety of radiotherapy followed by PD-1+ standard chemotherapy in the first-line treatment of initial unresectable rectal cancer liver metastases
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
30
Participants will receive Tislelizumab, 200mg, intravenously over 30 - 60 minutes, day 1 of every 3 weeks
Radiotherapy dose: 5×5 Gy
Participants will receive bevacizumab,5mg/kg,intravenously over 60 - 90 minutes, day 1 of every 2 weeks
progression free survival
The length of time from enrollment until the time of progression of disease (PFS, progression-free survival).
Time frame: up to 36 months
objective response rate
Clinical response of treatment according to RESIST v1.1 criteria (ORR, objective response rate).
Time frame: every 3 months (up to 36 months)
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Participants will receive Oxaliplatin,85mg/m2,day1
Participants will receive calcium folinate ,400mg/m2,day1
Participants will receive 5-fluorouracil ,400mg/m2,day1