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首页> 外文期刊>Cancer radiotherapie: journal de la Soci閠?fran鏰ise de radiotherapie oncologique >Evaluation of transit in vivo dosimetry using portal imaging and comparison with measurements using diodes [évaluation d'une dosimétrie in vivo de transit utilisant l'imageur portal et comparaison avec les mesures par diodes]
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Evaluation of transit in vivo dosimetry using portal imaging and comparison with measurements using diodes [évaluation d'une dosimétrie in vivo de transit utilisant l'imageur portal et comparaison avec les mesures par diodes]

机译:使用门禁成像评估体内剂量学,并与二极管进行比较[使用门禁成像仪评估体内剂量学,并与二极管测量结果进行比较]

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摘要

In vivo dosimetry transit using portal imaging is a promising approach for quality assurance in radiotherapy. A comparative evaluation was conducted between a commercial solution, EPIgray? and an in vivo dosimetry control reference using semiconductors diodes. Material and methods: The performance of the two in vivo dosimetry methods was assessed. The primary endpoint was the dose deviation between the reconstructed dose at the prescription point and the measured dose using the ionization chamber in phantoms or the calculated predictive dose by the treatment planning system with patients. The deviation threshold was set to. ±5%. In total, 107patients were prospectively included and treated with 3D-conformal radiotherapy (3D-CRT) or intensity-modulated radiotherapy (IMRT) techniques for tumours of the brain, chest and head and neck. Results: The dosimetric accuracy of EPIgray? in phantom were comparable to diodes in terms of repeatability (0.11%), reproducibility (0.29-0.51%) with a mean dose deviation of 0.17% (SD: 1.11). The rates of radiotherapy sessions out of the tolerance for the brain (3D-CRT and IMRT), thorax (3D-CRT) and the head and neck (IMRT) were respectively 0%, 9.6% and 5.3% with a mean dose deviation ranging between 0.49% and 1.53%. The mean of dose deviation between three consecutive sessions with EPIgray? validates 99.1% of treatments. Conclusion: The performance of EPIgray? in in vivo dosimetry is consistent with the recommendations of the European Society for Radiotherapy and Oncology (ESTRO) and equivalent to semiconductor diodes for 3D-CRT. It also allows adequate control for IMRT, which is technically difficult to perform with the diodes.
机译:使用门静脉成像的体内剂量测定转运是放射治疗质量保证的有前途的方法。在商业解决方案EPIgray?之间进行了比较评估。以及使用半导体二极管的体内剂量控制参考。材料和方法:评估了两种体内剂量测定法的性能。主要终点是处方点上的重建剂量与幻象中使用电离室测得的剂量之间的剂量偏差,或由患者的治疗计划系统计算出的预测剂量之间的剂量偏差。偏差阈值设置为。 ±5%。总共有107名患者被前瞻性纳入研究,并接受3D保形放射治疗(3D-CRT)或调强放射治疗(IMRT)技术治疗脑部,胸部,头部和颈部的肿瘤。结果:EPIgray的剂量学准确性?幻影中的幻影在重复性(0.11%),再现性(0.29-0.51%)方面与二极管相当,平均剂量偏差为0.17%(SD:1.11)。脑部(3D-CRT和IMRT),胸部(3D-CRT)和头颈(IMRT)耐受性之外的放射治疗率分别为0%,9.6%和5.3%,平均剂量偏差范围为在0.49%至1.53%之间。 EPIgray连续三个疗程之间的剂量偏差平均值?验证了99.1%的治疗。结论:EPIgray的性能如何?体内剂量测定中的剂量符合欧洲放射疗法和肿瘤学会(ESTRO)的建议,并且等效于3D-CRT的半导体二极管。它还允许对IMRT进行适当的控制,这在技术上很难用二极管执行。

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