About this trial
This is a prospective, single arm, phase II clinical study to evaluate the efficacy and safety of Zimberelimab combined with albumin-bound paclitaxel and cisplatin as neoadjuvant therapy for locally advanced cervical cancer.
Eligibility criteria
Qualifiers
Voluntary participation in clinical research.
Age ≥18 years old, female.
Squamous cell carcinoma, adenocarcinoma or adenosquamous carcinoma of the cervix confirmed by histology/cytology.
Previously untreated locally advancedcervical cancer (2018 FIGO stage IB3, IIA2) .
Disqualifiers
Patients with active autoimmune disease or a history of autoimmune disease.
Previous history of allogeneic hematopoietic stem cell transplantation or organ transplantation (except corneal transplantation).
Use of immunosuppressive drugs within 14 days prior to treatment, excluding nasal spray and inhaled corticosteroids or physiological doses of systemic steroids (i.e., not more than 10 mg/ day of prednisolone or another corticosteroid at the physiological dose of the drug).
Previous treatment with anti-PD-1 antibody, anti-PD-L1 antibody, anti-PD-L2 antibody, anti-CD137 antibody, or anti-lymphocyte antigen 4 (CTLA-4) antibody.
Trial design
Treatments tested in this trial
- Zimberelimab
- Albumin-bound Paclitaxel
- Cisplatin