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首页> 外文期刊>Technology in cancer research & treatment. >Evaluation of Photoneutron Dose Measured by Bubble Detectors in Conventional Linacs and Cyberknife Unit
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Evaluation of Photoneutron Dose Measured by Bubble Detectors in Conventional Linacs and Cyberknife Unit

机译:常规直线加速器和射波刀装置中气泡探测器测量的光中子剂量的评估

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This study aims to reduce the uncertainty about the photoneutron dose produced over a course of radiotherapy with high-energy photon beams and evaluate photoneutron contamination-based secondary malignancy risk for different treatment modalities. Dosimetric measurements were taken in Philips SL25/75, Elekta Synergy Platform (Elekta AB, Stockholm, Sweden), Varian Clinac DHX High Performance systems (Varian Medical Systems, Palo Alto, CA), and Cyberknife Robotic Radiosurgery Unit (Accuray Inc., Sunnyvale, CA) using bubble detector for neutron dosimetry. The measurement data were used to determine in-field and out-of-field neutron equivalent dose in 6-MV 3D conformal radiotherapy, sliding window–intensity-modulated radiotherapy, and stereotactic body radiotherapy and to calculate the effective dose in 18-MV 3D conformal radiotherapy and sliding window–intensity-modulated radiotherapy techniques for patients with prostate cancer undergoing a standard treatment. For the 18-MV treatment techniques, the secondary malignancy risk due to the neutron contamination was estimated using the risk factors published by The International Commission on Radiological Protection. The neutron contamination-based secondary malignancy risk for the 18-MV 3D conformal radiotherapy and sliding window–intensity-modulated radiotherapy modalities was found to be 0.44% and 1.45% for Elekta Synergy Platform and 0.92% and 3.0% for the Varian Clinac DHX High Performance, respectively. For 6-MV 3D conformal radiotherapy, sliding window–intensity-modulated radiotherapy, and stereotactic body radiotherapy treatment techniques, neutron equivalent doses inside the treatment field were found to be lower than 40 mSv. Our measurements reveal that equivalent dose and effective dose due to the neutron contamination are at a considerable level for 18-MV sliding window–intensity-modulated radiotherapy treatments, while 6-MV photon beams used in different modalities still induce only negligible photoneutrons. The secondary malignancy risk based on photoneutron should be therefore taken into consideration in case of selecting 18-MV photons in a sliding window–intensity-modulated radiotherapy treatment instead of 6 MV.
机译:这项研究旨在减少高能光子束放射治疗过程中产生的光中子剂量的不确定性,并评估不同治疗方式下基于光中子污染的继发性恶性肿瘤的风险。在飞利浦SL25 / 75,Elekta Synergy平台(Elekta AB,斯德哥尔摩,瑞典),Varian Clinac DHX高性能系统(Varian Medical Systems,帕洛阿尔托,CA)和射波刀机器人放射线外科装置(Accuray Inc.,桑尼维尔)进行剂量学测量(加利福尼亚州)使用气泡探测器进行中子剂量测定。测量数据用于确定6-MV 3D保形放射疗法,滑动窗口强度调制放射疗法和立体定向人体放射疗法的场内和场外中子当量剂量,并计算18-MV 3D的有效剂量保形放射治疗和滑动窗口强度调制放射治疗技术,用于接受标准治疗的前列腺癌患者。对于18-MV治疗技术,使用国际放射防护委员会发布的风险因素估算了由于中子污染而引起的继发性恶性肿瘤风险。对于Elekta Synergy Platform,18-MV 3D保形放射治疗和滑动窗口强度调制放射治疗方式基于中子污染的继发性恶性风险分别为0.44%和1.45%,Varian Clinac DHX High为0.92%和3.0%性能分别。对于6 MV 3D保形放射疗法,滑动窗口强度调制放射疗法和立体定向人体放射疗法治疗技术,发现治疗范围内的中子等效剂量低于40 mSv。我们的测量结果表明,对于18-MV滑动窗口强度调制的放射治疗,由于中子污染而产生的等效剂量和有效剂量处于相当高的水平,而在不同模式中使用的6-MV光子束仍然只能产生可忽略的光中子。因此,如果在滑动窗口强度调制放射治疗而不是6 MV中选择18 MV光子,则应考虑基于光中子的继发性恶性肿瘤风险。

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