Sci—Wed PM: Delivery—11: Dosimetric Properties of an EPID for Real‐Time Dose Verification

Abstract

PURPOSE: Dosimetric properties of an amorphous‐silicon electronic portal imaging device (EPID) operated in a real‐time acquisition mode were investigated. This mode will be essential for time‐resolved dose verification of dynamic‐IMRT and arc‐IMRT. METHODS: The EPID was used in continuous acquisition mode, where individual sequential image frames are acquired in real‐time. Properties studied include dose linearity and reproducibility. Summed continuous acquisition mode results were also compared to dose results using the well‐studied integrated acquisition mode, for example treatment deliveries including dynamic‐IMRT and single‐arc‐IMRT. Comparison was made using percentage dose difference of in‐field pixels (pixels >10% of maximum signal). Temporally‐resolved EPID response was also compared to that of ion‐chamber data for selected points in the deliveries. RESULTS: Using continuous acquisition mode, EPID response was not linear with dose, with response approximately corresponding to 1–1.5 missed images per irradiation. Reproducibility of EPID response improved with increasing MU. Analysis of the example irradiations revealed summed continuous acquisition mode compared well to integrated acquisition mode, within 2% of maximum dose for more than 95% of in‐field pixels. Time resolved EPID data compared well to ion chamber data, with dose increases/decreases overlying each other. CONCLUSION: Continuous acquisition mode is suited for time‐resolved dosimetry applications including single‐arc‐IMRT and dynamic IMRT, giving comparable dose results to the integrated acquisition mode. Linearity and reproducibility should be adequate for clinical applications although caution should be used in low MU work. Time‐resolved EPID dose information also compared well to time‐resolved ion‐chamber measurements.