Actively Recruiting
Bevacizumab Neoadjuvant Therapy for New High-grade Gliomas in the Brain
Led by The First Affiliated Hospital of Zhengzhou University · Updated on 2024-12-24
20
Participants Needed
1
Research Sites
117 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This research focuses on patients with new-onset high-grade gliomas, a type of brain tumor known as glioblastoma (GBM) that grows diffusely and invades surrounding brain tissue. The tumor's aggressive nature and its tendency to recur shortly after surgery contribute to poor outcomes. GBM is characterized by abnormal blood vessel growth, and blocking this process is a key therapeutic approach. The study aims to evaluate the safety and effectiveness of bevacizumab, a drug that inhibits blood vessel growth in tumors, when given before surgery as an additional treatment. Participants receive bevacizumab administered intravenously at a dose of 5 mg/kg on days 1 and 15 before surgery. This treatment is intended to reduce tumor blood vessel formation and limit tumor growth. The study does not mention other treatment groups or comparators but focuses on assessing bevacizumab as a neoadjuvant therapy to potentially improve surgical outcomes. During the study, researchers will monitor participants for approximately two years to measure the objective response rate, which reflects how well the tumor responds to treatment. Assessments may include imaging and clinical evaluations to track tumor status and patient health. Safety and tolerability of bevacizumab will also be closely observed throughout the treatment and follow-up periods, ensuring comprehensive monitoring of outcomes and adverse events.
CONDITIONS
Official Title
Bevacizumab Neoadjuvant Therapy for New High-grade Gliomas in the Brain
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 2 18 years or older
- Male or female
- Imaging diagnosis of high-grade glioma
- Karnofsky Performance Status (KPS) score of 60 or higher
You will not qualify if you...
- Previous treatment with anti-angiogenic targeted drugs
- Serious cardiac, pulmonary, hepatic, or renal disease
- History of arterial or venous blood clots within 6 months before screening
- Infectious diseases such as tuberculosis or viral hepatitis
- Uncontrolled high blood pressure, bleeding disorders, or unhealed wounds or fractures
- History of psychotropic substance abuse that cannot be stopped or mental disorders
- Abnormal blood clotting with bleeding tendency
- Conditions that make participation unsuitable, such as pregnancy or breastfeeding
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
The First Affiliated Hospital of Zhengzhou University
Zhengzhou, Henan, China
Actively Recruiting
Research Team
J
Junkuan Wang, M.D.
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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