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The investigator's study is a single armed phrase II trial ,aiming to improve the effecacy of treatment for advanced billiary tract cancer by means of Toripalimab combining with S1 and Albumin Paclitaxel as first line in patients with advanced Biliary Tract Cancer. treatment continually until disease progression or intolerable toxicity or Patients withdrawal of consent.and target sample is 30+ patients.
Toripalimab: 240 mg , once every 2-3 weeks; S1: 80-120mg, bid; oral, day1-14; Albumin paclitaxel: 120mg/m2 , administered on the first day and the eighth day of each cycle; 21 days for a treatment cycle
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Toripalimab Combined With S1 and Albumin Paclitaxel | Experimental |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Toripalimab Combined With S1 and Albumin Paclitaxel | Drug | Toripalimab 240 mg ,every 2-3 weeks S1:80-120mg,bid;oral,d1-14; Albumin Paclitaxel:120mg/m2,D 1 \8 |
|
| Measure | Description | Time Frame |
|---|---|---|
| objective response rate | ORR | 1 year |
| Measure | Description | Time Frame |
|---|---|---|
| progression free survival | PFS | 1 year |
| disease response rate | DCR | 1 year |
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Inclusion Criteria:
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Chinese PLA General Hospital | Recruiting | Beijing | Beijing Municipality | 100853 | China |
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| ID | Term |
|---|---|
| C079198 | S 1 (combination) |
| C481298 | theasinensin A |
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|
| overall survival |
OS |
| 1 year |