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Optimization of radiotherapy and chemotherapy for refractory glioblastoma based on molecular typing and exploration the predictive value of new molecular marker

Optimization of radiotherapy and chemotherapy regimen for refractory glioblastoma based on molecular typing and exploration the predictive value of new molecular marker

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IIR-17010327
Enrollment
Unknown
Registered
2017-01-04
Start date
2017-01-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

refractory glioblastoma

Interventions

Sponsors

Shanghai Jing'an District Central Hospital (Jing'an Huashan Hospital Branch, Fudan University)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1) postoperative histopathology and molecular confirmed MGMT promoter unmethylation in newly diagnosed GBM patients; 2) Aged 18-65 years old; 3) Karnofsky Performance Status (KPS) =60; 4) the expected survival time =3 months; 5) patients were without major organ dysfunction. Liver and kidney function was normal. Specific test index: White blood cells > 4.0×10^9/L; Platelet> 100×10^9/L; Hemoglobin > 10 g/dl; Serum bilirubin was lower than 1.5 times of the maximum normal value; ALT and AST was lower than 2 times of the maximum normal value; Serum creatinine = 1.5 mg/dl. 6) Patients fully understand clinical research protocol and signed the informed consent.

Exclusion criteria

Exclusion criteria: 1) Patients had undergone chemotherapy with TMZ before adjuvant radiotherapy; 2) Patient during pregnancy or lactation; 3) Patients with suppurative and chronic infectious wounds delayed healing; 4) Patients with liver, kidney and heart dysfunction; 5) Patients suffering from a history of mental illness and uneasily controlled epilepsy; 6) Patients was considered not suitable by researchers in this trial.

Design outcomes

Primary

MeasureTime frame
Progression Free Survival(PFS);Overall Survival(OS);Adverse Reactions;

Secondary

MeasureTime frame
Quality of Life;

Countries

China

Contacts

Public ContactYang Wang

Shanghai Jing'an District Central Hospital (Jing'an Huashan Hospital Branch, Fudan University)

wangdoctor@fudan.edu.cn+86 13918221522

Outcome results

None listed

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