Overview
Addition of Anlotinib Hydrochloride to the Stupp Regimen Versus the Stupp Regimen Alone for Newly Diagnosed Glioblastoma
Status:
Not yet recruiting
Not yet recruiting
Trial end date:
2024-12-01
2024-12-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
For patients with glioblastoma,postoperative radiotherapy combined with concurrent and adjuvant temozolomide (Stupp regimen) has long been considered a standard treatment approach.The treatment outcomes, however, are still dismal, with a median overall survival time of 8-12 months. As a novel small molecule multi-target tyrosine kinase inhibitor, anlotinib hydrochloride has been found to be able to inhibit both tumor angiogenesis and cell growth.Previous studies on recurrent glioblastoma have demonstrated its effectiveness in tumor control with manageable toxicities. The current study is designed to evaluate the efficacy and feasibility of the additional anlotinib hydrochloride to the Stupp regimen for newly diagnosed glioblastoma.Phase:
Phase 2Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
People's Hospital of GuangxiCollaborators:
Affiliated Hospital of Guilin University
Cancer Hospital of Guangxi Medical University
First Affiliated Hospital of Guangxi Medical University
LiuZhou People's Hospital
Liuzhou Worker's Hospital
Liuzhou Workers Hospital
Nanxishan HospitalTreatments:
Temozolomide
Criteria
Inclusion Criteria:- Newly diagnosed and histological proven glioblastoma
- Complete gross resection or subtotal resection
- Eastern Cooperative Oncology Group (ECOG) performance status of 0-2
- Adequate bone marrow, liver and renal function
- Written informed consent
Exclusion Criteria:
- Meningeal carcinomatosis or spinal compression
- Patients who have previously received chemotherapy, targeted therapy, or
anti-angiogenesis
- Active, known, or suspected autoimmune disease
- Severe allergy to anlotinib or temozolomide
- Patient having acute hepatitis virus infection, active tuberculosis, or other acute
infectious diseases
- Uncontrolled mental disorders
- High risk of bleeding
- Severe cardiovascular disease: myocardial ischemia or myocardial infarction above
grade II, poorly controlled arrhythmias (including men with QTc interval ≥ 450 ms,
women ≥ 470 ms), according to NYHA criteria; grades III to IV Insufficient function,
or cardiac color Doppler ultrasound examination indicates left ventricular ejection
fraction (LVEF) <50%
- Contraindicated for MRI examination
- Recipient of live vaccine prior to the first dose of anlotinib
- Ready for or previously received organ transplantation