Vinci Justin P, Hogstrom Kenneth R, Neck Daniel W
Department of Physics and Astronomy, Louisiana State University, Agricultural and Mechanical College, Baton Rouge, Louisiana 70803, USA.
Med Phys. 2008 Aug;35(8):3809-19. doi: 10.1118/1.2955751.
A system for measuring two-dimensional (2D) dose distributions in orthogonal anatomical planes in the cranium was developed and used to evaluate the accuracy of coplanar conformal therapy using ExacTrac image guidance. Dose distributions were measured in the axial, sagittal, and coronal planes using a CIRS (Computerized Imaging Reference Systems, Inc.) anthropomorphic head phantom with a custom internal film cassette. Sections of radiographic Kodak EDR2 film were cut, processed, and digitized using custom templates. Spatial and dosimetric accuracy and precision of the film system were assessed. BrainScan planned a coplanar-beam treatment to conformally irradiate a 2-cm-diameter x 2-cm-long cylindrical planning target volume. Prior to delivery, phantom misalignments were imposed in combinations of +/- 8 mm offsets in each of the principal directions. ExacTrac x-ray correction was applied until the phantom was within an acceptance criteria of 1 mm/1 degrees (first two measurement sets) or 0.4 mm/0.4 degrees (last two measurement sets). Measured dose distributions from film were registered to the treatment plan dose calculations and compared. Alignment errors, displacement between midpoints of planned and measured 70% isodose contours (Deltac), and positional errors of the 80% isodose line were evaluated using 49 2D film measurements (98 profiles). Comparison of common, but independent measurements of Deltac showed that systematic errors in the measurement technique were 0.2 mm or less along all three anatomical axes and that random error averaged [formula: see text] 0.29+/-0.06 mm for the acceptance criteria of 1 mm/1 degrees and 0.15 +/- 0.02 mm for the acceptance criteria of 0.4 mm/0.4 degrees. The latter was consistent with independent estimates that showed the precision of the measurement system was 0.3 mm (2sigma). Values of Deltac were as great as 0.9, 0.3, and 1.0 mm along the P-A, R-L, and I-S axes, respectively. Variations in Deltac along the P-A axis were correlated to misalignments between laser isocenter and radiation isocenter as documented by daily clinical Lutz tests. Based on results of comparisons of measured with calculated positions of the 80% dose lines along the major anatomical axes, a 1.25, 1.0, and 1.0 mm (0.75, 0.5, and 0.25 mm) gross tumor volume (GTV)-planning target volume (PTV) margin to account for delivery error would be appropriate for the P-A, R-L, and I-S axes, respectively, for an acceptance criteria of 1 mm/1 degrees (0.4 mm/0.4 degrees). It typically took 2 (3) ExacTrac x-ray image sets to achieve and verify acceptance criteria of 1 mm/1 degrees (0.4 mm/0.4 degrees). Our results demonstrated a measurement technique using a CIRS anthropomorphic head phantom with a modified film cassette, radiographic film (Kodak EDR2) with a custom film cutting template, and film dosimetry software has been developed and successfully applied to our clinic. It is recommended that a third party offer this service. Our goal of achieving accuracy of delivery of 1 mm or better in each of the three major anatomical axes was almost, but not quite achieved, not because of the accuracy of the image guidance system, but likely due to inaccuracy of laser isocenter and other systematic errors.
开发了一种用于测量颅骨正交解剖平面中二维(2D)剂量分布的系统,并使用该系统评估使用ExacTrac图像引导的共面适形治疗的准确性。使用带有定制内部胶片盒的CIRS(计算机化成像参考系统公司)人体头部模型在轴向、矢状和冠状平面测量剂量分布。使用定制模板对柯达EDR2射线照相胶片进行切割、处理和数字化。评估了胶片系统的空间和剂量准确性及精度。BrainScan计划进行共面束治疗,以适形照射直径2厘米×长2厘米的圆柱形计划靶体积。在治疗前,在每个主方向上以±8毫米偏移的组合施加模型错位。应用ExacTrac X射线校正,直到模型在1毫米/1度(前两组测量)或0.4毫米/0.4度(后两组测量)的验收标准范围内。将胶片测量得到的剂量分布与治疗计划剂量计算结果进行配准并比较。使用49次二维胶片测量(98条轮廓)评估对准误差、计划和测量的70%等剂量线中点之间的位移(Δc)以及80%等剂量线的位置误差。对常见但独立的Δc测量结果进行比较表明,测量技术在所有三个解剖轴上的系统误差均为0.2毫米或更小,对于1毫米/1度的验收标准,随机误差平均为0.29±0.06毫米,对于0.4毫米/0.4度的验收标准,随机误差平均为0.15±0.02毫米。后者与独立估计结果一致,表明测量系统的精度为0.3毫米(2σ)。沿前后(P-A)、左右(R-L)和上下(I-S)轴的Δc值分别高达0.9、0.3和1.0毫米。如日常临床Lutz测试所记录,沿P-A轴的Δc变化与激光等中心和辐射等中心之间的错位相关。基于沿主要解剖轴测量的80%剂量线位置与计算位置的比较结果,对于1毫米/1度(0.4毫米/0.4度)的验收标准,分别在P-A、R-L和I-S轴上设置1.25、1.0和1.0毫米(0.75、0.5和0.25毫米)的大体肿瘤体积(GTV)-计划靶体积(PTV)边界以考虑治疗误差是合适的。通常需要2(3)组ExacTrac X射线图像集才能达到并验证1毫米/1度(0.4毫米/0.4度)的验收标准。我们的结果表明,已开发出一种测量技术,该技术使用带有改良胶片盒的CIRS人体头部模型、带有定制胶片切割模板的射线照相胶片(柯达EDR2)以及胶片剂量测定软件,并已成功应用于我们的临床。建议由第三方提供此项服务。我们在三个主要解剖轴上实现1毫米或更好的治疗精度的目标几乎但未完全实现,这并非由于图像引导系统的精度问题,而是可能由于激光等中心的不准确性和其他系统误差。