RESUMO
We propose a method to incorporate independent verification of gantry angle for electronic portal imaging device (EPID)-based pre-treatment quality assurance (QA) of clinical volumetric modulated arc therapy (VMAT) plans. Gantry angle is measured using projections in the EPID of a custom phantom placed on the couch and the treatment plan is modified so as to be incident on the phantom with a portion of the beam that is collimated in the clinical plan. For our implementation, collimator and couch angles were set to zero and the inferior jaw and two most inferior multi-leaf collimator pairs were opened for the entire QA delivery. A phantom containing five gold coils was used to measure the gantry rotation through which each portal image was acquired. We performed the EPID QA for ten clinical plans and evaluated accuracy of gantry angle measurement, scatter incident on the imager due to the phantom, inter-image pixel linearity and inter- and intra-image noise. The gantry angle could be measured to within 0.0 ± 0.3° for static gantry and 0.2 ± 0.2° for arc acquisitions. Scatter due to the presence of the phantom was negligible. The procedure was shown to be feasible and adds gantry angle to the treatment planning parameters that can be verified by EPID-based pre-treatment VMAT QA.
Assuntos
Equipamentos e Provisões Elétricas , Planejamento da Radioterapia Assistida por Computador/instrumentação , Radioterapia de Intensidade Modulada/métodos , Estudos de Viabilidade , Imagens de Fantasmas , Controle de QualidadeRESUMO
PURPOSE: Significant anatomic and volumetric changes occur in head and neck cancer patients during fractionated radiotherapy, and the actual dose can be considerably different from the original plan. The purposes of this study were (1) to evaluate the differences between planned and delivered dose, (2) to investigate margins required for anatomic changes, and (3) to find optimal replanning strategies. METHODS AND MATERIALS: Eleven patients, each with one planning and six weekly helical CTs, were included. Intensity-modulated radiotherapy plans were generated using the simultaneous integrated boost technique. Weekly CTs were rigidly registered to planning CT before deformable registration was performed. The following replanning strategies were investigated with different margins (0, 3, 5 mm): midcourse (one replan), every other week (two replans), and every week (six replans). Doses were accumulated on the planning CT for comparison of various dose indices for target and critical structures. RESULTS: The cumulative doses to targets were preserved even at the 0-mm margin. Doses to cord, brainstem, and mandible were unchanged. Significant increases in parotid doses were observed. Margin reduction from 5 to 0 mm led to a 22% improvement in parotid mean dose. Parotid sparing could be preserved with replanning. More frequent replanning led to better preservation; replanning more than once a week is unnecessary. CONCLUSION: Shrinkage does not result in significant dosimetric difference in targets and critical structures, except for the parotid gland, for which the mean dose increases by approximately 10%. The benefit of replanning is improved sparing of the parotid. The combination of replanning and reduced margins can provide up to a 30% difference in parotid dose.