To evaluate the efficacy and safety of PD-1 immune checkpoint inhibitor combined with bevacizumab in the treatment of metastatic nasopharyngeal carcinoma after failure of platinum-based chemotherapy.
To evaluate the efficacy and safety of sintilimab combined with bevacizumab in the treatment of metastatic nasopharyngeal carcinoma (NPC) after platinum-based chemotherapy failure. The primary end point is objective response rate (ORR), the secondary end points are overall survival (OS), progression-free survival (PFS), duration of response (DOR), adverse effects and quality of life.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
33
Yanqun Xiang
Guangzhou, Guangdong, China
objective response rate (ORR)
The proportion of patients whose tumors shrink by a certain amount and remain in place for a certain amount of time, including complete response (CR) and partial response (PR).
Time frame: 2 years
overall survival (OS)
Patients in clinical trials were randomized to the time of death from any cause
Time frame: 2 years
progression-free survival (PFS)
36/5000 The time from the commencement of a randomized clinical trial to the progression of tumorigenesis (in any respect) or death from any cause.
Time frame: 2 years
duration of response (DOR)
The time between the first assessment of a tumor as CR or PR and the first assessment of PD or death from any cause.
Time frame: 2 years
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