Abstract
Simple SummaryRadiation therapy with protons facilitates highly conformal dose distributions. Thus, normal tissue can be spared effectively, which is a benefit, especially for children. Magnetic resonance imaging (MRI) is ideally suited to assess anatomical changes during the radiation course due to its superior soft tissue contrast and non-existent X-ray exposure. The MRI data have to be transformed to X-ray computed tomography (CT) images, which form the basis of treatment planning. This is conducted by capturing anatomical deformations between MRIs acquired at different times and by warping the planning CT according to these deformations. This procedure was applied in a prospective study enrolling pediatric head and neck cases. The preliminary evaluation of eleven patients with mainly rhabdomyosarcoma diagnosis and at craniofacial and base of skull tumor sites show that neither the deterioration of the target volume coverage nor an increased dose to organs-at-risk over the treatment course is a concern.Background and Purpose: Interfractional anatomical changes might affect the outcome of proton therapy (PT). We aimed to prospectively evaluate the role of Magnetic Resonance Imaging (MRI) based adaptive PT for children with tumors of the head and neck and base of skull. Methods: MRI verification images were acquired at half of the treatment course. A synthetic computed tomography (CT) image was created using this MRI and a deformable image registration (DIR) to the reference MRI. The methodology was verified with in-silico phantoms and validated using a clinical case with a shrinking cystic hygroma on the basis of dosimetric quantities of contoured structures. The dose distributions on the verification X-ray CT and on the synthetic CT were compared with a gamma-index test using global 2 mm/2% criteria. Results: Regarding the clinical validation case, the gamma-index pass rate was 98.3%. Eleven patients were included in the clinical study. The most common diagnosis was rhabdomyosarcoma (73%). Craniofacial tumor site was predominant in 64% of patients, followed by base of skull (18%). For one individual case the synthetic CT showed an increase in the median and dose on the spinal cord from 20.5 GyRBE to 24.8 GyRBE and 14.7 GyRBE to 25.1 GyRBE, respectively. Otherwise, doses received by OARs remained relatively stable. Similarly, the target volume coverage seen by and remained unchanged. Conclusions: The method of transferring anatomical changes from MRIs to a synthetic CTs was successfully implemented and validated with simple, commonly available tools. In the frame of our early results on a small cohort, no clinical relevant deterioration for neither PTV coverage nor an increased dose burden to OARs occurred. However, the study will be continued to identify a pediatric patient cohort, which benefits from adaptive treatment planning.
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