Impact of substructure radiation dose on health-related quality of life in children with brain tumors: a Pediatric Proton/Photon Consortium Registry (PPCR) study - Scorecard - MDSpire
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Impact of substructure radiation dose on health-related quality of life in children with brain tumors: a Pediatric Proton/Photon Consortium Registry (PPCR) study
Clinical Scorecard: Effects of Radiation Dose Distribution on Quality of Life in Pediatric Brain Tumor Survivors: Insights from the Pediatric Proton/Photon Consortium Registry (PPCR)
At a Glance
Category
Detail
Condition
Pediatric brain tumors treated with proton beam therapy
Key Mechanisms
Radiotherapy dose, fractionation, and volume of normal tissue exposure impact health-related quality of life (HRQoL)
Target Population
Children under 22 years treated with proton beam therapy for primary brain tumors
Care Setting
Multi-institutional pediatric oncology centers participating in the PPCR
Key Highlights
Radiotherapy dose to brain substructures correlates with neurocognitive, endocrine, and sensory toxicities affecting HRQoL.
Proton beam therapy offers superior normal tissue sparing compared to photon RT, potentially reducing adverse effects.
Patient-reported outcome measures (PedsQL) are essential for direct assessment of HRQoL in pediatric brain tumor survivors.
Guideline-Based Recommendations
Diagnosis
Use standardized delineation of intracranial substructures per published guidelines for accurate RT planning.
Collect comprehensive demographic, treatment, and imaging data to contextualize HRQoL outcomes.
Management
Prefer proton beam therapy over photon RT to minimize radiation dose to normal brain tissues.
Avoid partial RT courses and ensure complete treatment plans are retrievable for outcome analysis.
Monitoring & Follow-up
Administer PedsQL Generic Core and Infant Scales at baseline, end of RT, and annually for longitudinal HRQoL assessment.
Use both child self-report and parent-proxy reports depending on age to capture comprehensive HRQoL data.
Risks
Higher radiation doses to critical brain structures increase risk of neurocognitive decline, brain necrosis, cerebrovascular events, ototoxicity, visual toxicity, and endocrine dysfunction.
by Mikaela Doig, Jae Lee, Young Kwok, Iain MacEwan, Suzanne Wolden, Keith Allison, Sara Dennehy, Benjamin Bajaj, Michala Short, Peter Gorayski, Eva Bezak, Torunn I. Yock