Abstract

Patient‐specific pretreatment verification of intensity‐modulated radiation therapy (IMRT) or volumetric‐modulated arc therapy (VMAT) is strongly recommended for all patients in order to detect any potential errors in treatment planning process and machine deliverability, and is thus performed routinely in many clinics. Portal dosimetry is an effective method for this purpose because of its prompt setup, easy data acquisition, and high spatial resolution. However, portal dosimetry cannot be applied to IMRT or VMAT with flattening filter‐free (FFF) beams because of the high dose‐rate saturation effect of the electronic portal imaging device (EPID). In our current report, we suggest a practical QA method of expanding the conventional portal dosimetry to FFF beams with a QA plan generated by the following three steps: 1) replace the FFF beams with flattening filtered (FF) beams of the same nominal energy; 2) reduce the dose rate to avoid the saturation effect of the EPID detector; and 3) adjust the total MU to match the gantry and MLC leaf motions. Two RapidArc plans with 6 and 10 MV FFF beams were selected, and QA plans were created by the aforementioned steps and delivered. The trajectory log files of TrueBeam obtained during the treatment and during the delivery of QA plan were analyzed and compared. The maximum discrepancies in the expected trajectories between the treatment and QA plans were within 0.002 MU for the MU, 0.06° for the motion of gantry rotation, and 0.006 mm for the positions of the MLC leaves, indicating much higher levels of accuracy compared to the mechanical specifications of the machine. For further validation of the method, direct comparisons of the delivered QA FF beam to the treatment FFF beam were performed using film dosimetry and show that gamma passing rates under 2%/2 mm criteria are 99.0%–100% for the all four arc beams. This method can be used on RapidArc plans with FFF beams without any additional procedure or modifications on the conventional portal dosimetry of IMRT and is, therefore, a practical option for routine clinical use.PACS numbers: 87.53.Kn, 87.55.T‐, 87.56.bd, 87.59.‐e

Highlights

  • Two-dimensional array detectors are widely used for intensity-modulated radiation therapy (IMRT) quality assurance (QA), but may be inappropriate for pretreatment verification of stereotactic body radiation therapy (SBRT), which usually involves field sizes smaller than 5 × 5 cm2 due to its lower spatial resolution that results in coarse sample size insufficient for adequate gamma analysis

  • We suggest a practical QA method of expanding the conventional portal dosimetry to flattening filter-free (FFF) beams with a QA plan generated by the following three steps: 1) replace the FFF beams with flattening filtered (FF) beams of the same nominal energy; 2) reduce the dose rate to avoid the saturation effect of the electronic portal imaging device (EPID) detector; and 3) adjust the total MU to match the gantry and MLC leaf motions

  • Portal dosimetry IMRT QA was performed using the Varian Portal Dosimetry application (Ver. 10) by comparing the predicted dose images calculated from the Eclipse treatment planning system (TPS) with the measured dose images acquired from the amorphous silicon (aSi) imager

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Summary

Introduction

Portal dosimetry utilizing an electronic portal imaging device (EPID) is an attractive method for routine use because of its prompt setup, easy data acquisition, and high spatial resolution.[3] Varian Portal Dosimetry (Varian Medical System, Palo Alto, CA) is efficient for routine clinical use for IMRT QA due to its incorporation of an Eclipse treatment planning system and amorphous silicon (aSi) EPID. The official release of the TrueBeam system prohibits the use of portal dosimetry for FFF beams in order to prevent misuse with high dose rates of the FFF beams. Cumbersome procedures, such as transferring and processing of the measured image data, are mandatory if third party applications are used

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