Actively Recruiting
Neoadjuvant Therapy in Cervical Cancer
Led by Qilu Hospital of Shandong University · Updated on 2025-04-01
48
Participants Needed
1
Research Sites
101 weeks
Total Duration
On this page
Sponsors
Q
Qilu Hospital of Shandong University
Lead Sponsor
R
RemeGen Co., Ltd.
Collaborating Sponsor
AI-Summary
What this Trial Is About
In the comprehensive dataset of clinical diagnoses and treatments for cervical cancer in China, 49.8% of patients with stage IB3 and IIA2 receive surgical intervention following neoadjuvant chemotherapy. This indicates a pressing need to optimize neoadjuvant chemotherapy regimens for locally advanced cervical cancer. While paclitaxel combined with cisplatin is the conventional approach, 9.8% to 30.6% of patients demonstrate suboptimal responses, with a pathological complete response rate of approximately 10%. Currently, the efficacy of antibody-drug conjugates in neoadjuvant chemotherapy for cervical cancer remains unexplored. This study seeks to address this gap by evaluating the combination of Disitamab Vedotin and Cisplatin in patients with stage IB3 and IIA2 cervical cancer with positive HER2 expression.The study will assess the impact of this regimen on pathological complete response rates, surgical complications, surgical resection rates, and overall survival.
CONDITIONS
Official Title
Neoadjuvant Therapy in Cervical Cancer
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Clinical diagnosis of cervical squamous cell carcinoma
- HER-2 positive
- Female gender
- Age between 18 and 70 years
You will not qualify if you...
- Cervical adenocarcinoma
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Qilu Hospital of Shandong University
Jinan, Shandong, China, 250012
Actively Recruiting
Research Team
H
Hualei Bu
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
TREATMENT
Number of Arms
1
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