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Computational particle–haemodynamics analysis of liver radioembolization pretreatment as an actual treatment surrogate

血流动力学 医学 肝癌 导管 血流 放射科 癌症 动脉 核医学 内科学
作者
Jorge Aramburu,Raúl Antón,Alejandro Rivas,Juan Carlos Ramos,Bruno Sangro,José Ignacio Bilbao
出处
期刊:International Journal for Numerical Methods in Biomedical Engineering [Wiley]
卷期号:33 (2) 被引量:27
标识
DOI:10.1002/cnm.2791
摘要

Summary Liver radioembolization (RE) is a treatment option for patients with unresectable and chemorefractory primary and metastatic liver tumours. RE consists of intra‐arterially administering via catheter radioactive microspheres that locally attack the tumours, sparing healthy tissue. Prior to RE, the standard practice is to conduct a treatment‐mimicking pretreatment assessment via the infusion of 99m Tc‐labelled macroaggregated albumin microparticles. The usefulness of this pretreatment has been debated in the literature, and thus, the aim of the present study is to shed light on this issue by numerically simulating the liver RE pretreatment and actual treatment particle–haemodynamics in a patient‐specific hepatic artery under two different literature‐based cancer scenarios and two different placements of a realistic end‐hole microcatheter in the proper hepatic artery. The parameters that are analysed are the following: microagent quantity and size (accounting for RE pretreatment and treatment), catheter‐tip position (near the proper hepatic artery bifurcation and away from it), and cancer burden (10% and 30% liver involvement). The conclusion that can be reached from the simulations is that when it comes to mimicking RE in terms of delivering particles to tumour‐bearing segments, the catheter‐tip position is much more important (because of the importance of local haemodynamic pattern alteration) than the infused microagents (i.e. quantity and size). Cancer burden is another important feature because the increase in blood flow rate to tumour‐bearing segments increases the power to drag particles. These numerical simulation‐based conclusions are in agreement with clinically observed events reported in the literature. Copyright © 2016 John Wiley & Sons, Ltd.

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