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脑转移瘤临床试验中标准化脑肿瘤成像方案的共识建议。

Consensus recommendations for a standardized brain tumor imaging protocol for clinical trials in brain metastases.

机构信息

Department of Radiology, Mayo Clinic, Rochester, Minnesota, USA.

Department of Radiology and Nuclear Medicine, Erasmus Medical Center, University Medical Center Rotterdam, Rotterdam, Netherlands.

出版信息

Neuro Oncol. 2020 Jun 9;22(6):757-772. doi: 10.1093/neuonc/noaa030.

Abstract

A recent meeting was held on March 22, 2019, among the FDA, clinical scientists, pharmaceutical and biotech companies, clinical trials cooperative groups, and patient advocacy groups to discuss challenges and potential solutions for increasing development of therapeutics for central nervous system metastases. A key issue identified at this meeting was the need for consistent tumor measurement for reliable tumor response assessment, including the first step of standardized image acquisition with an MRI protocol that could be implemented in multicenter studies aimed at testing new therapeutics. This document builds upon previous consensus recommendations for a standardized brain tumor imaging protocol (BTIP) in high-grade gliomas and defines a protocol for brain metastases (BTIP-BM) that addresses unique challenges associated with assessment of CNS metastases. The "minimum standard" recommended pulse sequences include: (i) parameter matched pre- and post-contrast inversion recovery (IR)-prepared, isotropic 3D T1-weighted gradient echo (IR-GRE); (ii) axial 2D T2-weighted turbo spin echo acquired after injection of gadolinium-based contrast agent and before post-contrast 3D T1-weighted images; (iii) axial 2D or 3D T2-weighted fluid attenuated inversion recovery; (iv) axial 2D, 3-directional diffusion-weighted images; and (v) post-contrast 2D T1-weighted spin echo images for increased lesion conspicuity. Recommended sequence parameters are provided for both 1.5T and 3T MR systems. An "ideal" protocol is also provided, which replaces IR-GRE with 3D TSE T1-weighted imaging pre- and post-gadolinium, and is best performed at 3T, for which dynamic susceptibility contrast perfusion is included. Recommended perfusion parameters are given.

摘要

最近一次会议于 2019 年 3 月 22 日举行,参加方包括美国食品和药物管理局(FDA)、临床科学家、制药和生物技术公司、临床试验合作组和患者权益组织,会议讨论了增加中枢神经系统转移治疗药物开发的挑战和潜在解决方案。本次会议确定的一个关键问题是需要进行一致的肿瘤测量,以进行可靠的肿瘤反应评估,包括采用 MRI 方案进行标准化图像采集的第一步,该方案可应用于旨在测试新治疗药物的多中心研究。本文件是在先前关于高级别胶质瘤标准化脑肿瘤成像方案(BTIP)的共识建议基础上制定的,定义了一种脑转移瘤(BTIP-BM)方案,该方案解决了与评估中枢神经系统转移瘤相关的独特挑战。推荐的“最低标准”脉冲序列包括:(i)参数匹配的对比前和对比后反转恢复(IR)准备、各向同性 3D T1 加权梯度回波(IR-GRE);(ii)在注射钆基对比剂后和对比后 3D T1 加权图像之前采集的轴向 2D T2 加权涡轮自旋回波;(iii)轴向 2D 或 3D T2 加权液体衰减反转恢复;(iv)轴向 2D、3 个方向的扩散加权图像;和(v)对比后 2D T1 加权自旋回波图像,以提高病变的显影度。为 1.5T 和 3T MR 系统提供了推荐的序列参数。还提供了“理想”方案,该方案用 3D TSE T1 加权成像替代了 IR-GRE,在 3T 上进行最佳检查,其中包括动态磁敏感对比灌注。给出了推荐的灌注参数。

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