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CEM43对于热疗治疗监测而言是否仍是一个相关的热剂量参数?

Is CEM43 still a relevant thermal dose parameter for hyperthermia treatment monitoring?

作者信息

van Rhoon Gerard C

机构信息

a Department of Radiation Oncology , Hyperthermia unit, Erasmus MC Cancer Institute , Rotterdam , the Netherlands.

出版信息

Int J Hyperthermia. 2016;32(1):50-62. doi: 10.3109/02656736.2015.1114153. Epub 2016 Jan 12.

Abstract

CEM43 has its roots in the direct cytotoxic effect of heat, whereby the amount of cell death depends on the temperature and exposure time. CEM43 is a normalising method to convert the various time-temperature exposures applied into an equivalent exposure time expressed as minutes at the reference temperature of 43 °C. The CEM43 concept also holds a number of weaknesses, however. When used to predict treatment efficacy of combined radiotherapy plus hyperthermia, CEM43 does not include the effect of sensitisation by enhanced oxygenation, variation in interval time and the effect of multiple fractions. Further, it does not include the effect of increased perfusion at the lower thermal dose - and the occurrence of stasis at the higher thermal dose. Overall, studies towards a thermal dose-effect relationship in radiotherapy plus hyperthermia present a diffuse message without a definitive conclusion. However, prospective studies and studies with large patient numbers did report significant thermal dose-effect relationships and provide a good reason to continue research in the CEM43 model. Such research would be best performed in homogeneous patient groups with a single pathology and a low variation in tumour size and heterogeneity. Further, high quality thermometry, strict treatment schedules with fixed intervals and preferably homogenous heating are important requirements to enhance the probability of detecting a thermal dose-effect relationship. The slowly growing availability of hybrid MR hyperthermia systems should be a strong stimulus to expand these studies with the inclusion of measuring thermal dose-dependent blood flow and oxygen changes in the tumour and normal tissues.

摘要

CEM43源于热的直接细胞毒性作用,细胞死亡量取决于温度和暴露时间。CEM43是一种归一化方法,用于将所施加的各种时间-温度暴露转换为在43°C参考温度下以分钟表示的等效暴露时间。然而,CEM43概念也存在一些弱点。当用于预测放疗加高温治疗的疗效时,CEM43不包括增强氧合的致敏作用、间隔时间变化以及多次分割的影响。此外,它不包括较低热剂量下灌注增加的影响以及较高热剂量下出现的血流淤滞的影响。总体而言,关于放疗加高温治疗中热剂量-效应关系的研究呈现出分散的信息,没有明确的结论。然而,前瞻性研究和大样本患者研究确实报告了显著的热剂量-效应关系,并为继续在CEM43模型中开展研究提供了充分理由。此类研究最好在具有单一病理、肿瘤大小和异质性变化较小的同质患者群体中进行。此外,高质量的温度测量、固定间隔的严格治疗方案以及最好是均匀加热是提高检测热剂量-效应关系可能性的重要要求。混合式磁共振高温治疗系统的可用性逐渐增加,这应该是推动扩大这些研究的有力刺激因素,包括测量肿瘤和正常组织中热剂量依赖性血流和氧变化。

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