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Clinical Trials/NCT01635140
NCT01635140
Completed
Phase 3

Prospective Randomized Trial of Hypofractionated Radiotherapy Versus Conventional Radiotherapy in Diffuse Brainstem Glioma in Children.

Children's Cancer Hospital Egypt 573571 site in 1 country64 target enrollmentMay 2010

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Pediatric Brain Stem Glioma
Sponsor
Children's Cancer Hospital Egypt 57357
Enrollment
64
Locations
1
Primary Endpoint
Median overall-free survival
Status
Completed
Last Updated
13 years ago

Overview

Brief Summary

Hypofractionated radiotherapy reduce the patient and family burden through decreasing the overall treatment time. This study is to evaluate the clinical end results of the hypofractionated radiotherapy in DIPG compared to the conventional treatment. The non-inferiority of the hypofractionated radiotherapy will result in decrease the hospital, stay or engagement, for more than its half with the same results.

Detailed Description

In lack of open study protocols aiming to increase cure rate in pediatric diffuse intrinsic pontine glioma (DIPG), the investigators examined a hypofractionated radiotherapy regimen up to a dose of 39Gy in 13 fractions, completed in 2.5-3 weeks, instead of 6 weeks. This schedule offers a reduction in patient burden, especially preferable in children with a poor compliance and performance status. The non-inferiority of the hypofractionated regimen in its clinical end-results, with the reduction of the overall treatment time to less than its half will decrease the burden for the patient, his/her family and the treating department. This will be considered as added value without compromising the survival or increasing side effects.

Registry
clinicaltrials.gov
Start Date
May 2010
End Date
July 2011
Last Updated
13 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Children's Cancer Hospital Egypt 57357
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Newly diagnosed patients with a diffuse intrinsic brainstem glioma, ages 3-18years, were eligible for this protocol.
  • Patients were required to have symptoms for less than 3 months and at least two findings of the neurologic triad: cranial nerve deficits, ataxia, or long tract signs.
  • No performance criteria were required for entry onto the study.
  • The diagnosis of DIPG based on a high-quality, gadolinium- enhanced magnetic resonance imaging (MRI) scan containing at least T1, T2 MRIs with gadolinium contrast in three series, as well as diffusion imaging.
  • Symptoms \& signs of less than 3 months duration

Exclusion Criteria

  • Children were not eligible if they had received any prior therapy other than steroid
  • The diagnosis of exophytic brainstem glioma

Outcomes

Primary Outcomes

Median overall-free survival

Time Frame: 3 years

Progression-free survival

Time Frame: 3 Years

Study Sites (1)

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