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Y-90-Loaded Microsphere SIRT of HCC Patients With Portal Vein Thrombosis: High Clinical Impact of 99mTc-MAA SPECT/CT-Based Dosimetry

机译:HCC患者的Y-90加载的微球体血栓血栓形成:高临床影响99MTC-MAA SPECT / CT基剂量

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摘要

Radioembolization with Y-90-loaded microspheres based on classical prescription methods is increasingly applied to hepatocellular carcinoma (HCC) patients with portal vein thrombosis (PVT). In recent years, pretherapeutic predictive dosimetry based on technetium-99m macroaggregated albumin (MAA) quantitative scintigraphy using SPECT/CT has been developed. This paper presents an overview on the MAA-based dosimetry concept, discusses important confounding factors, such segmentation methods, and specific angiographic considerations required for a simulation-based dosimetric evaluation. The concept of "dosimetric angiography" is then introduced for the first time. Main results available are reported as a threshold tumor dose, allowing a response, between 100 and 120 Gy with Y-90-loaded resin microspheres and between 205 and 257 Gy with Y-90-loaded glass micro spheres. Impact of MAA-based dosimetry and MAA PVT targeting on overall survival is also reported. Due to those dosimetric advances, personalized dosimetric approaches based on MAA dosimetry are now available, with specific endpoints, for both Y-90-loaded resin or glass microsphere. The clinical impact of personalized dosimetry in PVT patients is particularly high, as a median overall survival of 20.2 months has been reported for good PVT candidate treated with glass microspheres (tumor-absorbed dose >= 205 Gy and good PVT targeting) as against only 3 months for poor candidate (tumor-absorbed dose <205 Gy or poor PVT targeting), and as a significant amount of patients where downstaged and resected (12%) in the same study. (C) 2019 Elsevier Inc. All rights reserved.
机译:基于经典处方方法的Y-90负载微球的放射性栓塞越来越多地应用于肝细胞癌(HCC)门静脉血栓形成(PVT)。近年来,已经开发了使用SPECT / CT的基于Technetium-99M大主角的白蛋白(MAA)定量Scintigraphy的Preterapeutic预测剂量。本文概述了基于MAA的剂量测定概念,讨论了重要的混淆因素,这种分割方法以及基于模拟的剂量测定评估所需的特定血管造影考虑因素。然后首次介绍“剂量测量血管造影”的概念。可获得的主要结果作为阈值肿瘤剂量,允许响应,100至120倍,在y-90加载的树脂微球和205和257g之间,用Y-90加载的玻璃微球。还报道了MAA基剂量测定和MAA PVT对整体存活的影响。由于这些剂量预处理,基于MAA剂量测定法的个性化剂量测定方法现在可用,具体的终点为Y-90负载树脂或玻璃微球。 PVT患者的个性化剂量术的临床影响特别高,因为用玻璃微球处理的良好PVT候选(肿瘤吸收剂量> = 205GY和良好的PVT靶向)据报道了20.2个月的总体生存率为20.2个月的中位数。候选人较差的月份(肿瘤吸收剂量<205 GY或PVT靶向差),以及作为同一研究中阶段和切除的大量患者(12%)。 (c)2019 Elsevier Inc.保留所有权利。

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  • 来源
    《Seminars in Nuclear Medicine》 |2019年第3期|共9页
  • 作者单位

    Canc Inst Eugene Marquis Dept Nucl Med CS 44229 F-35042 Rennes France;

    Canc Inst Eugene Marquis Dept Nucl Med CS 44229 F-35042 Rennes France;

    Canc Inst Eugene Marquis Dept Nucl Med CS 44229 F-35042 Rennes France;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 放射医学;
  • 关键词

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