About this trial
The purpose of this study is to assess the efficacy and safety of QL1706 combined with nab-paclitaxel and cisplatin in first-line therapy for patients with advanced or metastatic esophageal squamous cell carcinoma. QL1706 is a anti-PD-1 and anti-CTLA4 antibody.
Eligibility criteria
Qualifiers
Subjects participate voluntarily and sign informed consent.
18-75 years, male or female.
Histologically confirmed Unresectable Advanced or metastatic Esophageal Squamous Cell Carcinomas
No previous systemic anti-tumor treatment for unresectable locally advanced or metastatic esophageal squamous cell carcinoma has been received
Disqualifiers
Have received anti-PD-1 or anti-PD-L1 antibody therapy;
BMI < 18.5 kg/m2 or weight loss ≥ 10% within 2 months before screening (at the same time, the effect of a large amount of pleural effusions and ascites on bogy weight should be considered);
Presence of any active autoimmune disease or history of autoimmune disease (such as: Autoimmune hepatitis, interstitial pneumonia, uveitis, enteritis, hypophysitis, nephritis, hyperthyroidism)
Those who are taking immunosuppressants or systemic hormonal therapy for immunosuppressive purposes (dose> 10 mg/day prednisone or other equivalent cortiremonial hormones)
Trial design
Treatments tested in this trial
- QL1706 plus nab-paclitaxel and cisplatin
Treatment groups
Locations
Sponsors and collaborators
The First Affiliated Hospital of Henan University of Science and Technology
Lead sponsor