From the Center for Interventional Oncology, Radiology and Imaging Sciences, NIH Clinical Center (A.S.M., W.F.P., A.H.N., V.P.K., D.B.A., J.G.T., D.W., I.B., J.A.E.T., J.W.K., E.B.L., B.J.W.), National Institute of Biomedical Imaging and Bioengineering (B.J.W.), National Cancer Institute Center for Cancer Research (B.J.W.), and Biostatistics and Clinical Epidemiology Service, Clinical Center (P.G.W.), National Institutes of Health, 10 Center Dr, Bethesda, MD 20892, and Biocompatibles UK, BTG International Group, Camberley, England (S.L.W., A.L.L.).
Radiology. 2018 Nov;289(2):396-404. doi: 10.1148/radiol.2018172571. Epub 2018 Aug 14.
Purpose To correlate bead location and attenuation on CT images with the quantity and distribution of drug delivered to the liver following transarterial chemoembolization (TACE) with radiopaque drug-eluting beads (DEB) in a rabbit tumor model. Materials and Methods All procedures were performed with a protocol approved by the Institutional Animal Care and Use Committee. TACE was performed in rabbits (n = 4) bearing VX2 liver tumors by using radiopaque DEB (70-150 µm) loaded with doxorubicin (DOX). Livers were resected 1 hour after embolization, immediately frozen, and cut by using liver-specific three-dimensional-printed molds for colocalization of liver specimens and CT imaging. DOX penetration into tissue surrounding beads was evaluated with fluorescence microscopy. DOX levels in liver specimens were predicted by using statistical models correlating DOX content measured in tissue with bead volume and attenuation measured on CT images. Model predictions were then compared with actual measured DOX concentrations to assess the models' predictive power. Results Eluted DOX remained in close proximity (<600 µm) to beads in the liver 1 hour after TACE. Bead volume and attenuation measured on CT images demonstrated positive linear correlations (0.950 and 0.965, respectively) with DOX content in liver specimens. DOX content model predictions based on CT images were accurate compared with actual liver DOX levels at 1 hour. Conclusion CT may be used to estimate drug dose delivery and distribution in the liver following transarterial chemoembolization (TACE) with doxorubicin-loaded radiopaque drug-eluting beads (DEB). Although speculative, this informational map might be helpful in planning and understanding the spatial effects of TACE with DEB. © RSNA, 2018.
在兔VX2 肝癌模型中,通过经动脉化疗栓塞(TACE)将载多柔比星(DOX)的不透射线载药微球(DEB)注入肝脏,通过 CT 图像上的微球位置和衰减与 TACE 后药物在肝脏中的分布和数量进行相关性分析。
所有操作均按照机构动物护理和使用委员会批准的方案进行。将载 DOX 的不透射线 DEB(70-150 µm)用于 TACE,以兔 VX2 肝癌模型进行实验。栓塞后 1 小时切除肝脏,立即冷冻,使用肝脏特异性三维打印模具切割,以实现肝标本和 CT 图像的共定位。使用荧光显微镜评估 DOX 穿透微球周围组织的情况。通过将组织中 DOX 含量与 CT 图像上测量的微球体积和衰减相关联的统计模型来预测肝组织中 DOX 水平。然后将模型预测值与实际测量的 DOX 浓度进行比较,以评估模型的预测能力。
TACE 后 1 小时,DOX 从微球中洗脱出来并仍留在肝脏内,与微球接近(<600 µm)。CT 图像上测量的微球体积和衰减与肝组织中 DOX 含量呈正线性相关(分别为 0.950 和 0.965)。基于 CT 图像的 DOX 含量模型预测值与 1 小时时的实际肝 DOX 水平吻合良好。
CT 可用于预测 TACE 后载 DOX 的不透射线 DEB 在肝脏中的药物剂量分布。尽管这只是推测,但这种信息图可能有助于规划和理解 DEB 栓塞治疗的空间效应。
© 2018 RSNA