RecruitingPhase 2NCT06561308

Clinical Efficacy Study of PD-1 Inhibitor Combined With Neoadjuvant Chemotherapy in Advanced Endometrial Cancer

A Single-arm, Multicenter Phase II Study of PD-1 Inhibitor Combined With Neoadjuvant Chemotherapy in Advanced Endometrial Cancer in Clinical Efficacy


Sponsor

Women's Hospital School Of Medicine Zhejiang University

Enrollment

39 participants

Start Date

Sep 1, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

Exploring the therapeutic effect of neoadjuvant chemotherapy combined with PD-1 inhibitor camrelizumab on advanced stage III-IV endometrial cancer


Eligibility

Sex: FEMALEMin Age: 18 YearsMax Age: 75 Years

Plain Language Summary

Simplified for easier understanding

This study tests whether adding a PD-1 immune checkpoint inhibitor (immunotherapy) to standard chemotherapy before surgery improves outcomes for women with advanced endometrial cancer (uterine cancer) that is not yet operable due to its stage. **You may be eligible if...** - You are aged 18–75 with confirmed endometrial cancer at stage III (inoperable) or stage IV - Your cancer has not yet been treated - Your general health score is 0 or 1 (able to carry out normal activities) - Your blood counts and organ function are within acceptable ranges **You may NOT be eligible if...** - You have an active autoimmune disease (with limited exceptions) - You have previously received immunotherapy or immune checkpoint inhibitors - You have active hepatitis B, hepatitis C, HIV, or tuberculosis - You have had a prior bone marrow or organ transplant - You are pregnant or breastfeeding Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DRUGCamrelizumab

Camrelizumab is administered at 200mg, q3w,intravenous infusion

DRUGCarboplatin

AUC=4-6,q3w,intravenous infusion

DRUGPaclitaxel

175 mg/m2,q3w,intravenous infusion, administered over 30min.

PROCEDURESurgery

Transabdominal hysterectomy + bilateral adnexectomy + pelvic lymph node dissection + pelvic-abdominal tumor resection +/- para-abdominal aortic lymph node dissection


Locations(1)

Women's hospital school of medicine zhejiang university

Hangzhou, Zhejiang, China

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT06561308


Related Trials