Abstract
PurposeThe purpose of this study is to establish and assess a practical delivery quality assurance method for stereotactic radiosurgery with Cyberknife by analyzing the geometric and dosimetric accuracies obtained using a PTW31016 PinPoint ionization chamber and EBT3 films. Moreover, this study also explores the relationship between the parameters of plan complexity, target volume, and deliverability parameters and provides a valuable reference for improving plan optimization and validation.MethodsOne hundred fifty cases of delivery quality assurance plans were performed on Cyberknife to assess point dose and planar dose distribution, respectively, using a PTW31016 PinPoint ionization chamber and Gafchromic EBT3 films. The measured chamber doses were compared with the planned mean doses in the sensitive volume of the chamber, and the measured planar doses were compared with the calculated dose distribution using gamma index analysis. The gamma passing rates were evaluated using the criteria of 3%/1 mm and 2%/2 mm. The statistical significance of the correlations between the complexity metrics, target volume, and the gamma passing rate were analyzed using Spearman’s rank correlation coefficient.ResultsFor point dose comparison, the averaged dose differences (± standard deviations) were 1.6 ± 0.73% for all the cases. For planar dose distribution, the mean gamma passing rate for 3%/1 mm, and 2%/2 mm evaluation criteria were 94.26% ± 1.89%, and 93.86% ± 2.16%, respectively. The gamma passing rates were higher than 90% for all the delivery quality assurance plans with the criteria of 3%/1 mm and 2%/2 mm. The difference in point dose was lowly correlated with volume of PTV, number of beams, and treatment time for 150 DQA plans, and highly correlated with volume of PTV for 18 DQA plans of small target. DQA gamma passing rate (2%/2 mm) was a moderate significant correlation for the number of nodes, number of beams and treatment time, and a low correlation with MU.ConclusionPTW31016 PinPoint ionization chamber and EBT3 film can be used for routine Cyberknife delivery quality assurance. The point dose difference should be within 3%. The gamma passing rate should be higher than 90% for the criteria of 3%/1 mm and 2%/2 mm. In addition, the plan complexity and PTV volume were found to have some influence on the plan deliverability.
Highlights
Stereotactic radiosurgery (SRS) and stereotactic body radiotherapy (SBRT), with delivery of high biological effective dose (BED) and enhanced antitumor effect to improve the rate of local control or pain relief [1], have emerged as effective adjuvant and standalone treatment options for many kinds of cancers
The aim of this study is to evaluate two different DQA systems (PinPoint ionization chamber and BET3 films) for measuring point dose and planar dose distribution simultaneously for the Cyberknife pretreatment verification in various treatment sites, to establish a practical and efficient DQA method for Cyberknife system
Association of Physicists in Medicine (AAPM) TG135 recommended 2%/2mm criteria, we suggest that gamma passing rates above 90% using 3%/1 mm criteria can be used for Cyberknife DQA
Summary
Stereotactic radiosurgery (SRS) and stereotactic body radiotherapy (SBRT), with delivery of high biological effective dose (BED) and enhanced antitumor effect to improve the rate of local control or pain relief [1], have emerged as effective adjuvant and standalone treatment options for many kinds of cancers. To date, it has demonstrated a significant advantage over conventional external beam radiation therapy for relatively radioresistant tumors, such as non-small cell lung cancer and renal cell carcinoma [2, 3]. For high fraction dose radiotherapy with complex systems such as the Cyberknife (Accuray Incorporated, Sunnyvale CA, USA), a practical and efficient method for routine pretreatment verification is needed [5]
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