This is a single arm, multi-center Phase II Study. This clinical study is an investigator-initiated clinical trial(IIT). The objective of this study is to evaluate the efficacy and safety of Chemoradiationtherapy combined with QL1706 (anti-CTLA-4 and PD-1 antibody) in patients with unresectable locally advanced esophageal squamous cell carcinoma.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
39
QL1706 is a humanized anti-PD1 IgG4 and anti-CTLA-4 IgG4 antibody.
Tianjin cancer hospital
Tianjin, Tianjin Municipality, China
RECRUITINGPFS assessed by investigators
Progression-free survival assessed by investigators
Time frame: Up to approximately 2 years.
OS
Overall survival
Time frame: 1year and 3years
ORR
Objective Response Rate,Complete Response plus Partial Response
Time frame: Up to approximately 2 years
DoR
Duration of Response
Time frame: Up to approximately 2 years
The rates and severity of Adverse Events, Serious Adverse Events
The rates and severity of Adverse Events, Serious Adverse Events
Time frame: Through study completion, up to approximately 2 years
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