原发性中枢神经系统淋巴瘤:MRI和PET成像的进展。

Annals of lymphoma Pub Date : 2021-09-01 Epub Date: 2021-09-30 DOI:10.21037/aol-20-53
Prakash Ambady, Leland S Hu, Letterio S Politi, Nicoletta Anzalone, Ramon F Barajas
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引用次数: 7

摘要

对比增强磁共振成像(CE-MRI)仍然是原发性中枢神经系统淋巴瘤(PCNSL)患者初始检查、分期和治疗后反应评估的首选成像方式。虽然CE-MRI是一种检测血脑屏障(BBB)功能障碍的敏感测试,但它并不能从生物学上代表真正的肿瘤负担。目前的反应评估标准严重依赖于对比后t1加权(T1W)图像的二维解剖测量,以及对比前t2加权(T2W)成像。其他MRI特征,如弥散加权成像(DWI)和灌注加权成像,可以在大多数具有MRI能力的中心常规获得。新出现的证据支持整合这些数据,以更好地定义肿瘤生理学,并提供能够识别高风险亚群的额外有价值的临床工具,以及对治疗反应的早期预测。此外,新的先进的PCNSL分子和病理生理特征为有希望的靶向治疗方法提供了见解。然而,显著的机构成像差异和不一致的临床试验报告降低了PCNSL患者日常管理的可靠性、可重复性和最终翻译。在这里,我们回顾了已建立的神经影像学概念,并概述了有关可能改善诊断和反应评估的新型影像学技术的已发表文献。最后,我们强调了在早期PCNSL临床试验中对图像采集、后处理和新型成像生物标志物的标准化的需求。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Primary central nervous system lymphoma: advances in MRI and PET imaging.

Primary central nervous system lymphoma: advances in MRI and PET imaging.

Contrast enhanced magnetic resonance imaging (CE-MRI) remains the imaging modality of choice for initial workup, staging, and response assessment after therapy in patients with primary central nervous system lymphoma (PCNSL). While CE-MRI is a sensitive test to detect blood brain barrier (BBB) dysfunction, it does not biologically represent the true tumor burden. Current response assessment criteria relies heavily on two dimensional anatomical measurements on post contrast T1-weighted (T1W) images, as well as pre-contrast T2-weighted (T2W) imaging. Additional MRI features, such as diffusion-weighted imaging (DWI) and perfusion weighted imaging, can be routinely obtained at most centers with MRI capabilities. Emerging evidence supports the incorporation of these data to better define tumor physiology and provide additional valuable clinical tools capable of identifying high risk subgroups as well as early predictors of response to therapies. Further, novel advanced molecular and pathophysiologic characterization of PCNSL provides insights into promising targeted therapeutic approaches. However, significant institutional imaging variation and inconsistent clinical trial reporting diminishes the reliability, reproducibility and eventual translation in day to day management of patients with PCNSL. Here we review established neuroimaging concepts and provide an overview of published literature about novel imaging techniques that may improve diagnosis and response assessments. Finally, we highlight the need for standardization of image acquisition, post-processing, and incorporation of novel imaging biomarkers in early phase PCNSL clinical trials.

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