Vikraman Subramani, Manigandan Durai, Karrthick Karukkupalayam Palaniappan, Sambasivaselli Raju, Senniandavar Vellaingiri, Ramu Mahendran, Rajesh Thiyagarajan, Lutz Muller, Muthukumaran Manavalan, Karthikeyan Nithyanantham, Tejinder Kataria
Medanta The Medicity Hospital.
J Appl Clin Med Phys. 2014 Jan 7;16(1):5128. doi: 10.1120/jacmp.v16i1.5128.
The purpose of this study was to evaluate quantitatively the patient-specific 3D dosimetry tool COMPASS with 2D array MatriXX detector for stereotactic volumetric-modulated arc delivery. Twenty-five patients CT images and RT structures from different sites (brain, head & neck, thorax, abdomen, and spine) were taken from CyberKnife Multiplan planning system for this study. All these patients underwent radical stereotactic treatment in CyberKnife. For each patient, linac based volumetric-modulated arc therapy (VMAT) stereotactic plans were generated in Monaco TPS v3.1 using Elekta Beam Modulator MLC. Dose prescription was in the range of 5-20 Gy per fraction. Target prescription and critical organ constraints were tried to match the delivered treatment plans. Each plan quality was analyzed using conformity index (CI), conformity number (CN), gradient Index (GI), target coverage (TC), and dose to 95% of volume (D95). Monaco Monte Carlo (MC)-calculated treatment plan delivery accuracy was quantitatively evaluated with COMPASS-calculated (CCA) dose and COMPASS indirectly measured (CME) dose based on dose-volume histogram metrics. In order to ascertain the potential of COMPASS 3D dosimetry for stereotactic plan delivery, 2D fluence verification was performed with MatriXX using MultiCube phantom. Routine quality assurance of absolute point dose verification was performed to check the overall delivery accuracy. Quantitative analyses of dose delivery verification were compared with pass and fail criteria of 3 mm and 3% distance to agreement and dose differences. Gamma passing rate was compared with 2D fluence verification from MatriXX with MultiCube. Comparison of COMPASS reconstructed dose from measured fluence and COMPASS computed dose has shown a very good agreement with TPS calculated dose. Each plan was evaluated based on dose volume parameters for target volumes such as dose at 95% of volume (D95) and average dose. For critical organs dose at 20% of volume (D20), dose at 50% of volume (D50), and maximum point doses were evaluated. Comparison was carried out using gamma analysis with passing criteria of 3 mm and 3%. Mean deviation of 1.9% ± 1% was observed for dose at 95% of volume (D95) of target volumes, whereas much less difference was noticed for critical organs. However, significant dose difference was noticed in two cases due to the smaller tumor size. Evaluation of this study revealed that the COMPASS 3D dosimetry is efficient and easy to use for patient-specific QA of VMAT stereotactic delivery. 3D dosimetric QA with COMPASS provides additional degrees of freedom to check the high-dose modulated stereotactic delivery with very high precision on patient CT images.
本研究的目的是使用二维阵列MatriXX探测器对患者特异性三维剂量测定工具COMPASS进行定量评估,用于立体定向容积调强弧形放疗。本研究从赛博刀Multiplan计划系统中获取了25例来自不同部位(脑、头颈部、胸部、腹部和脊柱)的患者CT图像和放疗结构。所有这些患者均在赛博刀中接受了根治性立体定向治疗。对于每位患者,在Monaco TPS v3.1中使用医科达束流调制多叶准直器生成基于直线加速器的容积调强弧形放疗(VMAT)立体定向计划。剂量处方范围为每分次5-20 Gy。尝试使靶区处方和危及器官约束与所实施的治疗计划相匹配。使用适形指数(CI)、适形数(CN)、梯度指数(GI)、靶区覆盖度(TC)和95%体积剂量(D95)分析每个计划的质量。基于剂量体积直方图指标,使用COMPASS计算剂量(CCA)和COMPASS间接测量剂量(CME)对Monaco蒙特卡罗(MC)计算的治疗计划实施精度进行定量评估。为了确定COMPASS三维剂量测定用于立体定向计划实施的潜力,使用MultiCube模体通过MatriXX进行二维注量验证。进行绝对点剂量验证的常规质量保证以检查总体实施精度。将剂量实施验证的定量分析与3 mm和3%距离一致性和剂量差异的通过与不通过标准进行比较。将伽马通过率与使用MultiCube模体的MatriXX的二维注量验证进行比较。比较COMPASS从测量注量重建的剂量和COMPASS计算的剂量,结果显示与TPS计算剂量非常吻合。根据靶区体积的剂量体积参数(如95%体积剂量(D95)和平均剂量)对每个计划进行评估。对于危及器官,评估20%体积剂量(D20)、50%体积剂量(D50)和最大点剂量。使用3 mm和3%的通过标准进行伽马分析。观察到靶区体积95%体积剂量(D95)的平均偏差为1.9%±1%,而危及器官的差异要小得多。然而,由于肿瘤尺寸较小,在两例中观察到显著的剂量差异。本研究评估表明,COMPASS三维剂量测定对于VMAT立体定向放疗的患者特异性质量保证是高效且易于使用的。使用COMPASS进行三维剂量测定质量保证提供了额外的自由度,能够在患者CT图像上以非常高的精度检查高剂量调制的立体定向放疗。