Skip to content

The efficacy of the new chemotherapy regimen "TMZ+ABX" in the treatment of recurrent glioblastoma: A prospective, single-arm study

The efficacy of the new chemotherapy regimen "TMZ+ABX" in the treatment of recurrent glioblastoma: A prospective, single-arm study

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500106675
Enrollment
Unknown
Registered
2025-07-28
Start date
2025-08-31
Completion date
Unknown
Last updated
2025-08-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Recurrent glioblastoma

Interventions

The "TMZ+ABX" combined treatment group:"TMZ+ABX" combined treatment

Sponsors

Southern Medical University Southern Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1.Voluntarily sign the informed consent form; 2.Age: 18 to 70 years old, gender not limited; 3.Patients diagnosed with recurrent glioblastoma (WHO Grade IV) in accordance with the 2016 World Health Organization (WHO) glioma Diagnostic Guidelines, the 2022 National Health Commission Glioma Diagnosis and Treatment Guidelines of China, etc. 4.Preoperative KPS score >=60 points; 5.The standard for blood routine examination should meet the following requirements: ANC >=1.5×109/L; PLT >=90×109/L; Hb >=90g/L; 6.Biochemical tests must meet the following standards: TBIL=50 mL/min (CockcroftGault formula); 7.The coagulation test standards should comply with: International normalized ratio (INR) or prothrombin time (PT) =55%); 9.The Fridericia method corrected QT interval (QTcF) for electrocardiogram in females was less than 470 ms;

Exclusion criteria

Exclusion criteria: 1.Patients who are unable to undergo cranial MRI examinations; 2.Pregnant and lactating women; 3.Patients who were found to have active bleeding through cranial CT or MRI examination before enrollment; 4.A history of malignant tumors in other systems within the past 5 years; 5.Suffering from severe cardiovascular and respiratory system diseases; 6.Patients who, as determined by the researcher, are not suitable to participate in this trial; 7.There is a grade 3 or higher chronic toxic reaction according to the National Cancer Institute's Common Adverse Event Evaluation Criteria (NCI-CTCAE5.0);

Design outcomes

Primary

MeasureTime frame
Overall survival time;

Secondary

MeasureTime frame
Progression-free survival time;Objective response rate;

Countries

China

Contacts

Public ContactGuo-zhong Yi

Southern Medical University Southern Hospital

yiguozhong09@126.com+86 20 61641806

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026