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Optimization of radiotherapy and chemotherapy for refractory anaplastic astrocytoma based on molecular typing and exploration the predictive value of subtyping of the IDH/TERTp

Optimization of radiotherapy and chemotherapy for refractory anaplastic astrocytoma based on molecular typing and exploration the predictive value of subtyping of the IDH/TERTp

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IIR-17010500
Enrollment
Unknown
Registered
2017-01-23
Start date
2017-03-01
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 Anaplastic Astrocytoma

Interventions

control group:TMZ standard treatment

Sponsors

ShangHai Gamma Knife Hospital
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 anaplastic astrocytoma patients; (2) Aged 18-65 years old; (3) Karnofsky Performance Status (KPS) =60; (4) the expected survival time =6 months; (5) patients were without major organ dysfunction. 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) Patients 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; (7) Patients with contraindications to use DDP(such as allergy to Platinum-based drugs); (8) Patients participated in other clinical trials.

Design outcomes

Primary

MeasureTime frame
Progression Free Survival(PFS);Overall Survival(OS);RANO standard;Quality of Life;

Countries

China

Contacts

Public ContactYang Wang

ShangHai Gamma Knife Hospital

wangdoctor@fudan.edu.cn+86 13918221522

Outcome results

None listed

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