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Biodistribution pharmacokinetics and organ-level dosimetry for 188Re-AHDD-Lipiodol radioembolization based on quantitative post-treatment SPECT/CT scans

机译:基于定量后处理SPECT / CT扫描的188Re-AHDD-脂质碘栓栓塞的生物分布药代动力学和器官水平剂量测定

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摘要

BackgroundRhenium-188-labelled-Lipiodol radioembolization is a safe and cost-effective treatment for primary liver cancer. In order to determine correlations between treatment doses and patient response to therapy, accurate patient-specific dosimetry is required. Up to date, the reported dosimetry of 188Re-Lipiodol has been based on whole-body (WB) planar imaging only, which has limited quantitative accuracy. The aim of the present study is to determine the in vivo pharmacokinetics, bio-distribution, and organ-level dosimetry of 188Re-AHDD-Lipiodol radioembolization using a combination of post-treatment planar and quantitative SPECT/CT images. Furthermore, based on the analysis of the pharmacokinetic data, a practical and relatively simple imaging and dosimetry method that could be implemented in clinics for 188Re-AHDD-Lipiodol radioembolization is proposed.Thirteen patients with histologically proven hepatocellular carcinoma underwent 188Re-AHDD-Lipiodol radioembolization. A series of 2–3 WB planar images and one SPECT/CT scan were acquired over 48 h after the treatment. The time-integrated activity coefficients (TIACs, also known as residence-times) and absorbed doses of tumors and organs at risk (OARs) were determined using a hybrid WB/SPECT imaging method.
机译:背景188 188标记的脂质碘油放射栓塞术是一种用于原发性肝癌的安全且经济有效的治疗方法。为了确定治疗剂量和患者对治疗反应之间的相关性,需要准确的患者特异性剂量测定法。迄今为止,报道的 188 Re-Lipiodol剂量学仅基于全身(WB)平面成像,定量准确性有限。本研究的目的是结合后处理平面和定量SPECT /方法,确定 188 Re-AHDD-Lipiodol放射栓塞的体内药代动力学,生物分布和器官水平剂量学CT图像。此外,基于药代动力学数据的分析,提出了一种实用且相对简单的成像和剂量测定方法,可在临床中用于 188 Re-AHDD-Lipiodol放射栓塞治疗。13例经组织学证实的肝细胞癌患者癌行 188 Re-AHDD-Lipiodol放射栓塞术。治疗后48小时内,采集了一系列2–3 WB平面图像和一次SPECT / CT扫描。使用混合WB / SPECT成像方法确定时间积分活动系数(TIAC,也称为停留时间)和肿瘤和处于危险中的器官的吸收剂量(OAR)。

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