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在 aducanumab 的 1b 期 PRIME 研究中,参考和目标区域选择对淀粉样蛋白 PET SUVR 的影响。

Impact of Reference and Target Region Selection on Amyloid PET SUV Ratios in the Phase 1b PRIME Study of Aducanumab.

机构信息

Biogen, Cambridge, Massachusetts

Biospective Inc., Montréal, Quebec, Canada.

出版信息

J Nucl Med. 2019 Jan;60(1):100-106. doi: 10.2967/jnumed.118.209130. Epub 2018 May 18.

Abstract

SUV ratios (SUVRs) are commonly used to quantify tracer uptake in amyloid-β PET. Here, we explore the impact of target and reference region-of-interest (ROI) selection on SUVR effect sizes using interventional data from the ongoing phase 1b PRIME study (NCT01677572) of aducanumab (BIIB037) in patients with prodromal or mild Alzheimer disease. The florbetapir PET SUVR was calculated at baseline (screening) and at weeks 26 and 54 for patients randomized to receive placebo and each of 4 aducanumab doses (1, 3, 6, and 10 mg/kg) using the whole cerebellum, cerebellar gray matter, cerebellar white matter, pons, and subcortical white matter as reference regions. In addition to the prespecified composite cortex target ROI, individual cerebral cortical ROIs were assessed as targets. Of the reference regions used, subcortical white matter, cerebellar white matter, and the pons, alone or in combination, generated the largest effect sizes. The use of the anterior cingulate cortex as a target ROI resulted in larger effect sizes than the use of the composite cortex. SUVR calculations were not affected by correction for brain volume changes over time. Dose- and time-dependent reductions in the amyloid PET SUVR were consistently observed with aducanumab only in cortical regions prone to amyloid plaque deposition, regardless of the reference region used. These data support the hypothesis that florbetapir SUVR responses associated with aducanumab treatment are a result of specific dose- and time-dependent reductions in the amyloid burden in patients with Alzheimer disease.

摘要

SUV 比值(SUVRs)常用于量化淀粉样蛋白-β PET 中的示踪剂摄取。在此,我们使用正在进行的 aducanumab(BIIB037)治疗前驱期或轻度阿尔茨海默病患者的 1b 期 PRIME 研究(NCT01677572)的干预数据,探索目标和参考感兴趣区(ROI)选择对 SUVR 效应大小的影响。根据随机接受安慰剂和 aducanumab 4 种剂量(1、3、6 和 10mg/kg)的患者在基线(筛选)和 26 周和 54 周时的 florbetapir PET SUVR,使用全脑、小脑灰质、小脑白质、脑桥和皮质下白质作为参考区进行计算。除了预先指定的复合皮质靶 ROI 外,还评估了各个大脑皮质 ROI 作为靶区。在所使用的参考区中,皮质下白质、小脑白质和脑桥,单独或组合使用,产生了最大的效应大小。使用前扣带皮质作为靶 ROI 导致的效应大小大于使用复合皮质。SUVR 计算不受随时间变化的脑容量变化校正的影响。仅在皮质区域观察到 aducanumab 剂量和时间依赖性降低淀粉样蛋白 PET SUVR,无论使用何种参考区。这些数据支持这样的假设,即与 aducanumab 治疗相关的 florbetapir SUVR 反应是由于阿尔茨海默病患者淀粉样蛋白负担的特异性剂量和时间依赖性降低所致。

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