← Back to Clinical Trials
Recruiting Phase 2 NCT06532539

Cadonilimab With Chemoradiation for Recurrent and Oligometastatic Endometrial Carcinoma

Trial Parameters

Condition Endometrial Neoplasms
Sponsor Shandong Cancer Hospital and Institute
Study Type INTERVENTIONAL
Phase Phase 2
Enrollment 30
Sex FEMALE
Min Age 18 Years
Max Age 80 Years
Start Date 2024-06-13
Completion 2025-05
Interventions
Paclitaxel and CisplatinCadonilimabRadiotherapy

Brief Summary

The goal of this clinical trial is to evaluate the efficacy and safety of cadonilimab in combination with paclitaxel, cisplatin, and radiation therapy for the treatment of locally recurrent and oligometastatic endometrial carcinoma. The main questions it aims to answer are: 1. Does the combination therapy improve the overall response rate (ORR), progression-free survival (PFS), disease control rate (DCR), overall survival (OS), and safety in participants? 2. What are the predictive biomarkers of treatment efficacy, and how can this information better guide the use of immune-oncology drugs in combination therapy? Participants will: * Receive cadonilimab, paclitaxel, cisplatin, and radiation therapy according to a specified protocol. * Visit the clinic for regular checkups and tests throughout the treatment period. * Be monitored for and have records kept of ORR, PFS, DCR, OS, and safety. * Provide hematologic and tissue samples to explore biomarkers. This study will help determine if this combination therapy can become a new standard of care for patients with locally recurrent and oligometastatic endometrial carcinoma, as well as identify biomarkers to better guide treatment strategies.

Eligibility Criteria

Inclusion Criteria: 1. A written informed consent form must be signed before the implementation of any trial-related procedures. 2. Female, aged 18 years or older and 80 years or younger. 3. ECOG PS 0-1. 4. Newly diagnosed with histologically or cytologically confirmed primary endometrioid adenocarcinoma, serous carcinoma, clear cell adenocarcinoma, undifferentiated carcinoma, mixed cell adenocarcinoma, mesonephric adenocarcinoma, mucinous carcinoma, intestinal-type mesonephric-like adenocarcinoma, and carcinosarcoma, meeting the clinical diagnostic criteria for endometrial cancer. 5. Patients with locally recurrent or oligometastatic endometrial cancer after initial treatment. The number of recurrent and metastatic lesions is ≤5. Screening criteria for oligometastasis: lymph node metastases in the same region count as one metastatic lesion; liver metastases are limited to one; lung metastases are limited to three. 6. At least one site suitable for radiotherapy (including the primary l

Related Trials