Abstract
BackgroundConventional phantom-based planar dosimetry (2D-PBD) quality assurance (QA) using gamma pass rate (GP (%)) is inadequate to reflect clinically relevant dose error in intensity-modulated radiation therapy (IMRT), owing to a lack of information regarding patient anatomy and volumetric dose distribution. This study aimed to evaluate the dose distribution accuracy of IMRT delivery for nasopharyngeal carcinoma (NPC), which passed the 2D-PBD verification, using a measurement-guided 3D dose reconstruction (3D-MGR) method.MethodsRadiation treatment plans of 30 NPC cases and their pre-treatment 2D-PBD data were analyzed. 3D dose distribution was reconstructed on patient computed tomography (CT) images using the 3DVH software and compared to the treatment plans. Global and organ-specific dose GP (%), and dose-volume histogram (DVH) deviation of each structure was evaluated. Interdependency between GP (%) and the deviation of the volumetric dose was studied through correlation analysis.ResultsThe 3D-MGR achieved global GP (%) similar to conventional 2D-PBD in the same criteria. However, structure-specific GP (%) significantly decreased under stricter criteria, including the planning target volume (PTV). The average deviation of all inspected dose volumes (DV) and volumetric dose (VD) parameters ranged from − 2.93% to 1.17%, with the largest negative deviation in V100% of the PTVnx of − 15.66% and positive deviation in D1cc of the spinal cord of 6.66%. There was no significant correlation between global GP (%) of 2D-PBD or 3D-MGR and the deviation of the most volumetric dosimetry parameters (DV or VD), when the Pearson’s coefficient value of 0.8 was used for correlation evaluation.ConclusionEven upon passing the pre-treatment phantom based dosimetric QA, there could still be risk of dose error like under-dose in PTVnx and overdose in critical structures. Measurement-guided 3D volumetric dosimetry QA is recommended as the more clinically efficient verification for the complicated NPC IMRT.
Highlights
Conventional phantom-based planar dosimetry (2D-PBD) quality assurance (QA) using gamma pass rate (GP (%)) is inadequate to reflect clinically relevant dose error in intensity-modulated radiation therapy (IMRT), owing to a lack of information regarding patient anatomy and volumetric dose distribution
Reconstructed dose-volume histogram (DVH) The average relative difference in the volumetric dose (DV) and dose volume (VD) between the 3D dose reconstruction and the planned dose ranged from − 2.93% to 0.02% for planning target volume (PTV), and − 1.66% to 1.17% for Organ at risk (OAR) (Table 2)
Traditional 2D Phantom QA and global GP (%) evaluation is not sufficient for ensuring the clinically accurate volumetric dose for IMRT treatment, as there is no strong correlation between the global GP (%) and percentage deviation in DVH of both PTVs and OAR, even when a strict 1%/1 mm gamma criterion was used
Summary
Conventional phantom-based planar dosimetry (2D-PBD) quality assurance (QA) using gamma pass rate (GP (%)) is inadequate to reflect clinically relevant dose error in intensity-modulated radiation therapy (IMRT), owing to a lack of information regarding patient anatomy and volumetric dose distribution. Patient-specific pre-treatment quality assurance (QA) is necessary for the implementation of IMRT [3], and it has been a consensus of the researcher community that patient-specific QA can be done by film dosimetry combined with ionization chambers measurement [4,5,6], or by a 2D/3D detector arrays test in a phantom to compare and validate the dose accuracy of the treatment [7,8,9,10] Most of these pre-treatment QA use the ‘γ evaluation method’ for the result analysis, which is a composite analysis of distanceto-agreement (DTA) and dose difference (DD) [11,12,13]. It has raised a question whether the patient OARs are safe or if the PTVs are covered by the prescribed dose when a higher passing rate is achieved
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