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Outcomes Following Proton Therapy for Pediatric Low-Grade Glioma
Daniel J Indelicato1, Ronny L Rotondo1, Haruka Uezono1
1Department of Radiation Oncology, University of Florida College of Medicine, Jacksonville, Florida.
Insights
Proton therapy for pediatric low-grade glioma (LGG) shows promising 5-year survival rates of 92% and good local control. This treatment reduces radiation to healthy tissue, leading to fewer acute toxicities in children with brain tumors.
Area of Science:
- Pediatric Oncology
- Radiation Oncology
- Neuro-Oncology
Background:
- Proton therapy offers dosimetric advantages for pediatric low-grade glioma (LGG) by reducing radiation dose to uninvolved tissues.
- LGG is the fourth most common pediatric tumor treated with proton therapy, but clinical outcome data are limited.
Purpose of the Study:
- To assess the clinical outcomes, efficacy, and toxicity of proton therapy in children with low-grade glioma.
- To analyze patient, tumor, and treatment-related variables influencing outcomes.
Main Methods:
- Retrospective review of 174 children (≤21 years) with nonmetastatic LGG treated with proton therapy (2007-2017).
- Assessment of clinical outcomes (local control, progression-free survival, overall survival) and toxicity.
- Univariate analysis of prognostic factors.
Main Results:
- 5-year actuarial rates: local control 85%, progression-free survival 84%, overall survival 92%.
- Brainstem/spinal cord location and dose <54 GyRBE were associated with inferior local control (P < .01).
- Notable toxicities included hormone deficiency (22%), pseudoprogression (32.1%), and rare serious events like brainstem necrosis (1.1%).
Conclusions:
- Proton therapy demonstrates favorable efficacy in pediatric LGG, with high survival rates and good local control.
- This approach reduces radiation dose to developing brain tissue, diminishing acute toxicities compared to photon therapy without compromising disease control.
Purpose:
Dosimetric studies show that proton therapy can reduce the low/intermediate radiation dose to uninvolved tissue in children with low-grade glioma (LGG). For this reason, LGG is the fourth most common pediatric tumor treated with proton therapy, yet clinical outcome data on efficacy and toxicity are limited.
Methods And Materials:
We reviewed the medical records of 174 children (≤21 years old) with nonmetastatic LGG enrolled on a prospective protocol and treated with proton therapy between 2007 and 2017. We assessed clinical outcomes and toxicity and analyzed patient, tumor, and treatment-related variables.
Results:
The median age was 10.2 years (range, 2-21). Fifty-eight percent of tumors were World Health Organization grade 1 and 30% were grade 2; 12% were diagnosed on imaging characteristics alone. The most common histology was pilocytic astrocytoma (47%). The most common tumor subsites were diencephalon/optic pathway (52%), caudal brainstem (16%), and cerebellum (13%). Forty-two percent received chemotherapy before radiation therapy. The median follow-up was 4.4 years. The 5-year actuarial rates of local control, progression-free survival, and overall survival were 85% (95% confidence interval [CI], 78%-90%), 84% (95% CI, 77%-89%), and 92% (95% CI, 85%-95%), respectively. On univariate analysis, brainstem/spinal cord tumor location (62% vs 90% elsewhere) and dose <54 GyRBE (67% vs 91% for 54 GyRBE) were associated with inferior local control (P < .01 for both). Twenty-two patients (12.6%) experienced acute nausea or vomiting requiring ondansetron; 2 patients (1.1%) required corticosteroids. Serious toxicities (4% of patients) included brainstem necrosis requiring corticosteroids (n = 2), symptomatic vasculopathy (n = 2), radiation retinopathy (n = 1), epilepsy (n = 1), and death from radiation-induced high-grade glioma (n = 1). Thirty-nine patients (22%) developed new-onset central hormone deficiency. Pseudoprogression was observed in 32.1%.
Conclusions:
Compared with modern photon series, proton therapy reduces the radiation dose to developing brain tissue, diminishing acute toxicities without compromising disease control.
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