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Clinical Trial Summary

This is a multi-centre prospective, non-inferiority trial. Patients will be randomized to two treatment groups in a 1:1 ratio and will be stratified by age, Karnofsky Performance Status and extent of the surgical resection.

This study will assess the effect of a one-week radiotherapy regimen in comparison with a three-week radiotherapy regimen on the survival of elderly and/or frail patients with glioblastoma multiforme (Frail: ≥>50 years old and with a KPS of 50% or less50%-70%; Elderly and frail: ≥65 years and with a KPS of 50% - 70%; Elderly: ≥65 years and with a KPS of 80% - 100%).


Clinical Trial Description

This is a multi-centre prospective, non-inferiority trial. Patients will be randomized to two treatment groups in a 1:1 ratio and will be stratified by:

- Age (<65 and ≥65 years old)

- Karnofsky Performance Status (≤70 and > 7050 or higher)

- Extent of the resection at surgery (biopsy only versus complete/near total and gross total or incomplete /partial resection)

Randomization:

Patients will be randomized to receive one of the two following treatments:

Arm 1:

- Short Radiotherapy

- 25 Gy/5 fractions

- 1 week (5 fractions per week)

Arm 2:

- Regular Radiotherapy

- 40 Gy/15 fractions

- 3 weeks (5 fractions per week) ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01450449
Study type Interventional
Source International Atomic Energy Agency
Contact
Status Completed
Phase Phase 3
Start date February 2009
Completion date November 2014

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