Patients were aged \>18 years with histological confirmed GC/EGJC and were refractory to the first line of therapy. Additional eligibility requirements included: ≥1 measurable disease at baseline per Response Evaluation Criteria in Solid Tumors, version 1.1 (RECIST v 1.1); Eastern Cooperative Oncology Group Performance status of 0 or 1; or life expectancy of ≥ 3 months and adequate organ function. The main exclusion criteria were interstitial lung disease, pulmonary fibrosis, active or prior autoimmune disease or active hepatitis, or history of anlotinib or any other PD-L1/PD-1 antagonist treatment. Patients with abdominal fistula, diverticulitis, gastrointestinal ulcerative disease or perforation, or abdominal abscess within the prior 4 weeks were also excluded. This study was an open, exploratory single-arm, phase II trial. Enrolled patients received anlotinib (12mg, po. qd, d1-14) combined with toripalimab (240 mg, inv, over 30 min once every 2 weeks).
Study Type
OBSERVATIONAL
Enrollment
62
Mutation of FGFR2
Xiaochun Zhang
Qingdao, China
RECRUITINGORR
Time frame: 01.01.2019 to 01.01.2021
6m-PFS
Time frame: 01.01.2019 to 01.01.2021
safety
Time frame: 01.01.2019 to 01.01.2021
PFS
Time frame: 01.01.2019 to 01.01.2021
OS
Time frame: 01.01.2019 to 01.01.2021
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.