The purpose of this study is to test the the efficacy and safety of sintilimab in combination with chemoradiation before surgery for esophageal cancer.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
20
Other Name: (IBI308)
carboplatin AUC 2/paclitaxel 50 mg/m2 weekly
IMRT or VMAT
Zhejiang Cancer Hospital
Hangzhou, Zhejiang, China
RECRUITINGunacceptable toxicity
"Unacceptable toxicity" is defined as any of the following toxicities: \>1 episode of grade 3/4 neutropenia or thrombocytopenia \<75,000/μL (despite prior dose reduction) during chemoradiation any toxicity that results in \>2 week cumulative delay in chemoradiation any toxicity that is attributed to durvalumab which results in a delay of \>8 weeks in surgery, i.e. surgery \>16 weeks from the end of radiation, for a potentially operable patient any reason that is attributed to durvalumab which leads to death within 30 days of surgery
Time frame: 1 year
pathologic complete response rate, pCR
Time frame: 1 year
major pahological response, MPR
Time frame: 1 year
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