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Prospective study of intensity-modulated radiation therapy using standard radiation dose for high-grade glioma

Prospective study of intensity-modulated radiation therapy using standard radiation dose for high-grade glioma - IMRT using standard radiation dose for HGG

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000022502
Enrollment
20
Registered
2016-05-27
Start date
2016-05-30
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

High-grade glioma

Interventions

The prescribed dose of IMRT is 60 Gy in 30 fractions over 6 weeks (2 Gy per fraction, five fractions per week). The chemotherapy regimens are not regulated.

Sponsors

Kagawa University Hospital
Lead Sponsor
Department of Neurosurgery, Kagawa University, Faculty of Medicine
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Histologically proven high-grade glioma 2. No tumor recognized in the brainstem and optic nerve on preoperative MRI 3. Planning target volume (irradiated 60Gy) is less than 1/3 of the brain volume 4. Aged 20 to 75 years old 5. ECOG performance status of 0,1 or 3 due to neurological signs caused by the tumor 6. Written informed consent

Exclusion criteria

Exclusion criteria: 1. No prior radiation therapy for intracranial disease 2. Prior treatment for high-grade glioma 3. Women during pregnancy, possible pregnancy, or breast-feeding, patient who wish pregnancy 4. Psychiatric disease 5. Inappropriate patients for this study judged by physicians

Design outcomes

Primary

MeasureTime frame
Overall survival

Secondary

MeasureTime frame
Progression-free survival, Completion rate of IMRT, Grade 3 or more non-hematological toxicity evaluated every 12 months

Countries

Japan

Contacts

Public ContactShigeo Takahashi

Kagawa University Hospital Department of Radiation Oncology

takahashi.shigeo@kagawa-u.ac.jp087-898-5111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026