ctDNA-guided First-line Immuno-de-escalation Therapy for IVB-stage and Recurrent Cervical Cancer

NANot yet recruitingINTERVENTIONAL
Enrollment

20

Participants

Timeline

Start Date

March 10, 2025

Primary Completion Date

December 31, 2028

Study Completion Date

December 31, 2028

Conditions
Uterine Cervical Neoplasm
Interventions
DRUG

cadonilimab combined with cisplatin-based chemotherapy ± bevacizumab

Patients with persistent, recurrent, or advanced metastatic cervical cancer who have not received systemic treatment are treated with cadonilimab combined with cisplatin-based chemotherapy ± bevacizumab (treatment dosage: cadonilimab 10 mg/kg, paclitaxel 175 mg/m\^2, cisplatin 50 mg/m\^2, cisplatin AUC 4-5, bevacizumab 7.5-15 mg/kg), once every 3 weeks, for a total of 6 cycles (if the patient continues to benefit, chemotherapy is allowed beyond 6 cycles), followed by maintenance treatment with cadonilab ± bevacizumab.

Trial Locations (1)

200090

The Obstetrics and Gynecology Hospital of Fudan University, Shanghai

All Listed Sponsors
lead

Obstetrics & Gynecology Hospital of Fudan University

OTHER