The aim of this single center, single arm and prospective study is to explore the safety and efficacy of Oncolytic virus Plus Anti-PD1 and Chemotherapy as Preoperative therapy for Patients with Borderline Resectable and Locally Advanced Pancreatic Cancer
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
20
Oncolytic virus,Camrelizumab ,AG(Gemcitabine +Capecitabine )
West China Hospital, Sichuan University
Chengdu, Sichuan, China
Incidence of Treatment-Related Adverse Events [Safety and Tolerability]
Defined by treatment-related adverse events as assessed by CTCAE v4.0
Time frame: through study completion, an average of 1 year
R0 resection rate
defined as complete resection without any macroscopic or microscopic evidence of lesion at the lateral and deep tissue margins
Time frame: 6 months
ORR
The incidence of CR (complete remission) and PR (partial remission)
Time frame: 6 months
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