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首页> 外文期刊>Radiotherapy and oncology: Journal of the European Society for Therapeutic Radiology and Oncology >Pre-treatment dosimetric verification by means of a liquid-filled electronic portal imaging device during dynamic delivery of intensity modulated treatment fields.
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Pre-treatment dosimetric verification by means of a liquid-filled electronic portal imaging device during dynamic delivery of intensity modulated treatment fields.

机译:在动态传输强度调制治疗场期间,通过充液电子门成像设备进行预处理剂量学验证。

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BACKGROUND AND PURPOSE: Although intensity modulated radiation therapy is characterized by three-dimensional dose distributions which are often superior to those obtained with conventional treatment plans, its routine clinical implementation is partially held back by the complexity of the beam verification. This is even more so when a dynamic multileaf collimator (dMLC) is used instead of a segmented beam delivery. We have therefore investigated the possibility of using a commercially available, liquid-filled electronic portal imaging device (EPID) for the pre-treatment quality assurance of dynamically delivered dose distributions. METHODS AND MATERIALS: A special acquisition mode was developed to optimize the image acquisition speed for dosimetry with the liquid-filled EPID. We investigated the accuracy of this mode for 6 and 18 MV photon beams through comparison with film and ion chamber measurements. The impact of leaf speed and pulse rate fluctuations was quantified by means of dMLC plans especially designed for this purpose. Other factors influencing the accuracy of the dosimetry (e.g. the need for build-up, remanence of the ion concentration in the liquid and bulging of the liquid at non-zero gantry angles) were studied as well. We finally compared dosimetric EPID images with the corresponding image prediction delivered without a patient in the beam. RESULTS: The dosimetric accuracy of the measured dose distribution is approximately 2% with respect to film and ion chamber measurements. The accuracy declines when leaf speed is increased beyond 2 cm/s, but is fairly insensitive to accelerator pulse rate fluctuations. The memory effect is found to be of no clinical relevance. When comparing the acquired and expected distributions, an overall agreement of 3% can be obtained, except at areas of steep dose gradients where slight positional shifts are translated into large errors. CONCLUSIONS: Accurate dosimetric images of intensity modulated beam profiles delivered with a dMLC can be obtained with a commercially available, liquid-filled EPID. The developed acquisition mode is especially suited for fast and accurate pre-treatment verification of the intensity modulated fields.
机译:背景与目的:尽管强度调制放射疗法的特征在于三维剂量分布,通常优于传统治疗方案所获得的剂量分布,但其常规的临床实施因光束验证的复杂性而部分受到阻碍。当使用动态多叶准直器(dMLC)代替分段光束传输时,情况更是如此。因此,我们研究了使用可商购的充满液体的电子门成像设备(EPID)来动态分配剂量的预处理质量保证的可能性。方法和材料:开发了一种特殊的采集模式,以优化使用液体填充EPID进行剂量测定的图像采集速度。通过与薄膜和离子室测量结果的比较,我们研究了该模式对6和18 MV光子束的准确性。通过为此目的专门设计的dMLC计划量化了叶片速度和脉搏率波动的影响。还研究了影响剂量测定精度的其他因素(例如,是否需要堆积,液体中离子浓度的剩余以及在非零机架角度的液体膨胀)。最后,我们将剂量学EPID图像与相应的图像预测结果进行了比较,而无需患者在光束中。结果:相对于薄膜和离子室测量,所测量剂量分布的剂量学准确性约为2%。当叶片速度增加到超过2 cm / s时,精度会下降,但是对加速器脉冲速率波动不敏感。发现记忆效应与临床无关。当比较获取的分布和预期的分布时,可以得到3%的总体一致性,除了在陡峭的剂量梯度区域,轻微的位置偏移会转化为较大的误差。结论:dMLC传送的强度调制光束轮廓的精确剂量图像可以通过市售的充满液体的EPID获得。所开发的采集模式特别适合于对强度调制场进行快速,准确的预处理验证。

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