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Reproducibility of target volumes generated using uncoached 4-dimensional CT scans for peripheral lung cancer

机译:使用未指导的4维CT扫描生成的周围型肺癌目标体积的可重复性

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Background 4-dimensional CT (4DCT) scans are increasingly used to account for mobility during radiotherapy planning. As variations in respiratory patterns can alter observed motion, with consequent changes in the generated target volumes, we evaluated the reproducibility of 4D target volumes generated during repeat uncoached quiet respiration. Methods A retrospective analysis was performed on two successive scans (4DCT1 and 4DCT2) generated at the same scanning session for 26 patients with peripheral lung cancer treated with stereotactic radiotherapy (SRT). The volume and position of planning target volumes (PTV4DCT1 and PTV4DCT2) contoured on both scans were compared, and a dosimetric analysis performed. A SRT plan optimized for each PTV was sequentially applied to the other PTV, and coverage by the 80% isodose was evaluated. Color intensity projections (CIP) were used to evaluate regions of underdosage. Results No significant volumetric differences were observed between the two PTVs (t-Test p = 0.60). The average displacement of the center of mass between corresponding PTVs was 1.4 ± 1.0 mm, but differences in position were 2.0 mm or greater in 5 cases (19%). Coverage of both PTVs by the 80% prescription isodose exceeded 90% for all but one patient. For the latter, the prescription isodose covered only 82.5% of PTV4DCT1. CIP analysis revealed that the region of underdosage was an end-inspiratory position occupied by the tumor for only 10–20% of the respiratory cycle. Conclusion In nearly all patients with stage I lung cancer, the PTV derived from a single uncoached 4DCT achieves dosimetric coverage that is similar to that achieved using two such consecutive scans.
机译:背景4维CT(4DCT)扫描越来越多地用于放射治疗计划中的可移动性。由于呼吸模式的变化会改变观察到的运动,从而导致生成的目标体积发生变化,因此,我们评估了在重复的无教练安静呼吸过程中生成的4D目标体积的可重复性。方法对26例接受立体定向放疗(SRT)治疗的周围型肺癌患者,在同一次扫描中连续两次扫描(4DCT1和4DCT2)进行回顾性分析。比较在两次扫描中绘制轮廓的计划目标体积(PTV 4DCT1 和PTV 4DCT2 )的体积和位置,并进行剂量分析。将针对每个PTV优化的SRT计划依次应用于其他PTV,并评估80%的等剂量剂量的覆盖率。颜色强度预测(CIP)用于评估剂量不足的区域。结果两个PTV之间没有观察到明显的体积差异(t检验p = 0.60)。相应PTV之间的质心平均位移为1.4±1.0 mm,但5例(19%)的位置差异为2.0 mm或更大。除一名患者外,所有处方药的80%的等剂量剂量都覆盖了90%以上的PTV。对于后者,处方等剂量仅覆盖了PTV 4DCT1 的82.5%。 CIP分析显示,剂量不足的区域是在呼吸周期的10%至20%内肿瘤占据的吸气末位置。结论在几乎所有I期肺癌患者中,源自单个未指导4DCT的PTV的剂量学覆盖率均类似于使用两次此类连续扫描所获得的剂量覆盖率。

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