The overall objective of this study is to determine the efficacy of weekly Vinblastine in chemotherapy naïve patients with progressive or incompletely resected paediatric low grade glioma, to generate estimates of the response rate, progression-free survival, toxicity and quality of daily living among the population treated and determine biologic factors which will enable us to predict tumour behaviour.
Unresectable low grade glioma (LGG) of childhood increasingly appears as a chronic condition for which multiple treatments may be required. While several studies have shown evidence of short term tumour control with chemotherapy, the progression-free survival at 5 years is unsatisfactory. In addition, several regimens currently used for this condition are associated with significant risks of side effect and long term toxicity. We have piloted in a single arm study the feasibility and efficacy of Vinblastine for children with recurrent and refractory low grade glioma, who have failed at least one line of treatment (chemotherapy and/or irradiation). Preliminary results show promising activity with minimal toxicity.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
50
Vinblastine dose: 6 mg/m2 (10 mg maximum dose) route intravenous administration once a week.
Alberta Children's Hospital
Calgary, Alberta, Canada
Stollery Children's Hospital
Edmonton, Alberta, Canada
The response rate to weekly vinblastine
Time frame: 70 Weeks
The progression-free survival with Vinblastine
Time frame: At one year, two years and three years
The quality of daily life during treatment
Time frame: 26 Weeks
The correlation of biological features of LGG with tumour behaviour
Time frame: 5 years
To determine the role of telomere maintenance in the prognosis and evolution of PLGG
Time frame: 5 years
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