Department of Radiation Oncology, University of Iowa, Iowa City, Iowa, USA.
Int J Radiat Oncol Biol Phys. 2013 Jun 1;86(2):387-93. doi: 10.1016/j.ijrobp.2012.12.026. Epub 2013 Feb 20.
To present a novel marker-flange, addressing source-reconstruction uncertainties due to the artifacts of a titanium intracavitary applicator used for magnetic resonance imaging (MRI)-guided high-dose-rate (HDR) brachytherapy (BT); and to evaluate 7 different MRI marker agents used for interstitial prostate BT and intracavitary gynecologic HDR BT when treatment plans are guided by MRI.
Seven MRI marker agents were analyzed: saline solution, Conray-60, copper sulfate (CuSO4) (1.5 g/L), liquid vitamin E, fish oil, 1% agarose gel (1 g agarose powder per 100 mL distilled water), and a cobalt-chloride complex contrast (C4) (CoCl2/glycine = 4:1). A plastic, ring-shaped marker-flange was designed and tested on both titanium and plastic applicators. Three separate phantoms were designed to test the marker-flange, interstitial catheters for prostate BT, and intracavitary catheters for gynecologic HDR BT. T1- and T2-weighted MRI were analyzed for all markers in each phantom and quantified as percentages compared with a 3% agarose gel background. The geometric accuracy of the MR signal for the marker-flange was measured using an MRI-CT fusion.
The CuSO4 and C4 markers on T1-weighted MRI and saline on T2-weighted MRI showed the highest signals. The marker-flange showed hyper-signals of >500% with CuSO4 and C4 on T1-weighted MRI and of >400% with saline on T2-weighted MRI on titanium applicators. On T1-weighted MRI, the MRI signal inaccuracies of marker-flanges were measured <2 mm, regardless of marker agents, and that of CuSO4 was 0.42 ± 0.14 mm.
The use of interstitial/intracavitary markers for MRI-guided prostate/gynecologic BT was observed to be feasible, providing accurate source pathway reconstruction. The novel marker-flange can produce extremely intense, accurate signals, demonstrating its feasibility for gynecologic HDR BT.
提出一种新的标记法兰,解决由于用于磁共振成像(MRI)引导高剂量率(HDR)近距离放射治疗(BT)的钛腔内施源器的伪影而导致的源重建不确定性;并评估用于间质前列腺 BT 和腔内妇科 HDR BT 的 7 种不同的 MRI 标记剂,当治疗计划由 MRI 引导时。
分析了 7 种 MRI 标记剂:生理盐水、康瑞-60、硫酸铜(CuSO4)(1.5g/L)、液体维生素 E、鱼油、1%琼脂糖凝胶(每 100mL 蒸馏水 1g 琼脂糖粉末)和钴-氯络合物对比剂(C4)(CoCl2/甘氨酸=4:1)。设计了一种塑料环形标记法兰,并在钛和塑料施源器上进行了测试。设计了三个单独的体模,分别用于测试标记法兰、前列腺 BT 的间质导管和妇科 HDR BT 的腔内导管。对每个体模中的所有标记物进行了 T1-和 T2 加权 MRI 分析,并与 3%琼脂糖凝胶背景进行了百分比量化。使用 MRI-CT 融合测量了标记法兰的 MR 信号的几何精度。
T1 加权 MRI 上的 CuSO4 和 C4 标记物以及 T2 加权 MRI 上的生理盐水显示出最高的信号。在钛施源器上,CuSO4 和 C4 上的 T1 加权 MRI 上标记法兰的信号高于 500%,生理盐水上的 T2 加权 MRI 上的信号高于 400%。在 T1 加权 MRI 上,标记法兰的 MRI 信号误差无论标记物如何,均小于 2mm,CuSO4 的误差为 0.42±0.14mm。
观察到用于 MRI 引导的前列腺/妇科 BT 的间质/腔内标记物的使用是可行的,提供了准确的源路径重建。新型标记法兰可以产生极其强烈、准确的信号,证明其在妇科 HDR BT 中的可行性。