核磁共振测温技术的验证:肿瘤热疗的小动物模型。

S A Pahernik, M Peller, M Dellian, R Loeffler, R Issels, M Reiser, K Messmer, A E Goetz
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引用次数: 9

摘要

背景:局部热疗已被证明是一种有效的辅助治疗癌症。然而,这种治疗方式的进展需要对整个肿瘤的温度分布进行非侵入性评估,以便对所有肿瘤区域进行有效的热剂量管理。磁共振成像(MR)提供了一种很有前途的工具来量化、非侵入性和三维肿瘤内的温度分布。考虑到肿瘤在热疗过程中病理生理变化与温度敏感MR参数之间复杂的相互关系的动物模型是开发和验证新的MR测温技术的必要条件。方法:实验设置允许在体内标准化条件下同时测量温度,肿瘤血流和温度敏感的MR参数。在吸入麻醉下,对7只患有无黑色素瘤的叙利亚金仓鼠进行44摄氏度的局部热疗20分钟。光纤探头用于参考温度测量。激光多普勒血流仪用于在线肿瘤血流测定,磁共振测温采用纵向T1弛豫时间测量。结果:实验设计实现了多功能磁共振测温。肿瘤T1松弛时间分别为1.44 s(1.36, 1.46)和1.53 s(1.36, 1.46)。48, 1.75),分别在37℃和44℃热疗期间(中位数分别为25%和75%;结论:这种新颖的体内模型为磁共振热成像方法的开发和验证提供了标准化的研究。
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Validation of MR thermometry technology: a small animal model for hyperthermic treatment of tumours.

Background: Local hyperthermia has been shown to be an effective adjuvant therapy for cancer. However, progress in this treatment modality requires the non-invasive assessment of temperature distribution in the entire tumour to enable administration of an efficient thermal dose to all tumour areas. Magnetic resonance (MR) imaging offers a promising tool to quantify, non-invasively and three-dimensionally, temperature distribution within tumours. An animal model taking into account the complex interrelationship between pathophysiological changes within a tumour during hyperthermia and temperature-sensitive MR parameters is warranted for the development and validation of new MR thermometry technology.

Methods: An experimental set-up was implemented to allow simultaneous measurements of temperature, tumour blood flow and temperature-sensitive MR parameters under standardised conditions in vivo. Local hyperthermia was induced at 44 degrees C for 20 min under inhalation anaesthesia on seven Syrian Golden hamsters bearing an amelanotic melanoma. Fibreoptic probes were used for reference temperature measurements. Laser Doppler flowmetry served for on-line tumour blood flow determination, and MR thermometry was performed using longitudinal T1 relaxation time measurements.

Results: The experimental design enables multifunctional MR thermometry. T1 relaxation times of tumours were 1.44 s (1.36, 1.46) and 1.53 s (1. 48, 1.75) at 37 degrees C and during hyperthermia at 44 degrees C, respectively (median, 25% and 75% quartiles, respectively; P<0.05). At the end of 20 min of hyperthermic treatment at 44 degrees C, relative tumour blood flow was reduced to 40.5% (20.7, 43.3) compared to values before treatment (median, 25% and 75% quartiles, respectively; P<0.05). Imaging of T1 relaxation times revealed a heterogeneous distribution in temperature during hyperthermic treatment.

Conclusion: This novel in vivo model allows standardised investigations for the development and validation of MR thermography methods.

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