Radiation therapy remains a cornerstone in the management of both benign and malignant intracranial tumors, either as monotherapy or combined with surgery and/or chemotherapy. Despite its therapeutic benefits, it is frequently associated with potential long-term adverse effects, with neurotoxicity posing a major challenge, especially in young patients affected by benign primary tumors.
In the brain, late radiotoxicities typically manifest as cognitive dysfunction, leukoencephalopathy, brain atrophy, brain tissue necrosis, cerebrovascular complications, endocrinopathies, and/or secondary malignant neoplasms. Radiation-induced hippocampal injury, in particular, significantly contributes to cognitive impairment, while broader central nervous system effects arise through multiple mechanisms, including vascular injury, neuronal depletion, chronic inflammation, demyelination, and tissue necrosis. The severity of cognitive dysfunction depends on multiple factors, including the location and the volume of the tumor, the total radiation dose administered, the fractionation regimen, and the individual susceptibility of the patient, as well as comorbidities (e.g., diabetes, etc.) and concomitant drugs. The distinct physical characteristics of proton therapy, such as a reduced entrance dose, an eliminated exit dose, and a Bragg peak, provide clear dosimetric advantages over conventional photon treatments. Pencil-beam scanning further improves on earlier passive scattering approaches by delivering modulated proton beamlets for superior target conformality and reduced neutron scatter, thereby limiting low- and intermediate- dose exposure to cranial organs at risk (OARs) while preserving adequate dose coverage within the target volume. From a radiobiological standpoint, these properties suggest that proton therapy may present a more favorable risk-benefit balance compared to photon-based modalities, particularly for long-term clinical outcomes. It achieves a drastic reduction in the integral dose, offering substantial benefit in decreasing radiation-induced second malignancies, making it mandatory for children when available. Proton therapy is well established for treating pediatric tumors, CNS tumors such as low-grade gliomas (LGG) and meningiomas, especially if near the optic pathway or brainstem, and all the benign tumors in young patients. In these cases, the primary goal extends beyond curing the disease to preserving neurological and cognitive functions.
Study Type
OBSERVATIONAL
Enrollment
60
European Institute of Oncology, Milan
Milan, Italy, Italy
The presence of cognitive impairment
The primary endpoint will be the presence of cognitive impairment during the first 5 years after enrollment, as measured by a comprehensive neuropsychological assessment.
Time frame: From the end of Protontherapy through study completion, an average of 1 year.
Perceived cognitive impairment
For Functional Assessment of Cancer Therapy-cognition (FACT-cog) 37 items will be completed (score 1-4)
Time frame: At baseline (pre - Protontherapy), 6 and 12 months post-treatment, and then annually for 5 years.
Depressive symptoms
At Beck Depression Inventory-II (BDI-II) 21 items will be completed (score 0-3)
Time frame: At baseline (pre - Protontherapy), 6 and 12 months post-treatment, and then annually for 5 years.
Anxiety
For State-Trait Anxiety Inventory (STAI) 40 items will be completed (score 1-4)
Time frame: At baseline (pre - Protontherapy), 6 and 12 months post-treatment, and then annually for 5 years.
Quality of Life data (QoL) - EORTC QLQ C30 questionnaires.
For EORTC QLQ C30, 30 items will be completed (score 1-4).
Time frame: At baseline (pre - Protontherapy), 6 and 12 months post-treatment, and then annually for 5 years.
Sleep quality
For Pittsburgh Sleep Quality Index (PSQI) 24 items will be completed (score 0-3)
Time frame: At baseline (pre - Protontherapy), 6 and 12 months post-treatment, and then annually for 5 years.
Cognitive Reserve
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For Cognitive Reserve Index questionnaire (CRIq) 20 items will be completed (core 0-1)
Time frame: At baseline (pre - Protontherapy), 6 and 12 months post-treatment, and then annually for 5 years.
Global functioning
For Montreal Cognitive Assessment (MoCA) 30 items will be completed (score 1-5).
Time frame: At baseline (pre - Protontherapy), 6 and 12 months post-treatment, and then annually for 5 years.
Learning and Verbal Memory
For Rey Auditory Verbal Learning Test (RAVLT) 15 items will be completed (score 0-4).
Time frame: At baseline (pre - Protontherapy), 6 and 12 months post-treatment, and then annually for 5 years.
Working memory
For Corsi Span backward/forward 18 items will be completed (score 0-4).
Time frame: At baseline (pre - Protontherapy), 6 and 12 months post-treatment, and then annually for 5 years.
Visual memory
For Rey-Osterrieth complex figure -recall 18 items will be completed (score 0-2).
Time frame: At baseline (pre - Protontherapy), 6 and 12 months post-treatment, and then annually for 5 years.
Visuospatial abilities
For Rey-Osterrieth complex figure -copy 18 items will be completed (score 0-2).
Time frame: At baseline (pre - Protontherapy), 6 and 12 months post-treatment, and then annually for 5 years.
Executive function
For Frontal Assessment Battery (FAB) 30 items will be completed (score 0-3).
Time frame: At baseline (pre - Protontherapy), 6 and 12 months post-treatment, and then annually for 5 years.
Attention
For Symbol digit modalities test (SDMT) 110 items will be completed (score 0-1)
Time frame: At baseline (pre - Protontherapy), 6 and 12 months post-treatment, and then annually for 5 years.