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治疗前 Ferumoxytol 增强 MRI 预测转移性乳腺癌对脂质体伊立替康的反应。

Pretherapy Ferumoxytol-enhanced MRI to Predict Response to Liposomal Irinotecan in Metastatic Breast Cancer.

机构信息

From the Departments of Cancer Physiology (H.R., A.M.A.L., N.R.), Radiology (J.R.C., D.K.J.), and Breast Oncology (H.S.H.), Moffitt Cancer Center, 12902 Magnolia Dr, Tampa, FL 33612; Ipsen Bioscience, Cambridge, Mass (S.G.K.); HonorHealth Research Institute, Scottsdale, Ariz (J.C.S.); Imaging Endpoints Core Laboratory, Scottsdale, Ariz (R.L.K.); and Department of Oncologic Sciences, University of South Florida, Tampa, Fla (N.R.).

出版信息

Radiol Imaging Cancer. 2023 Mar;5(2):e220022. doi: 10.1148/rycan.220022.

Abstract

Purpose To investigate ferumoxytol (FMX)-enhanced MRI as a pretreatment predictor of response to liposomal irinotecan (nal-IRI) for thoracoabdominal and brain metastases in women with metastatic breast cancer (mBC). Materials and Methods In this phase 1 expansion trial (ClinicalTrials.gov identifier, NCT01770353; 27 participants), 49 thoracoabdominal (19 participants; mean age, 48 years ± 11 [SD]) and 19 brain (seven participants; mean age, 54 years ± 8) metastases were analyzed on MR images acquired before, 1-4 hours after, and 16-24 hours after FMX administration. In thoracoabdominal metastases, tumor transverse relaxation rate (R*) was normalized to the mean R* in the spleen (rR*), and the tumor histogram metric rR*, representing the average of rR* in voxels above the th percentile, was computed. In brain metastases, a novel compartmentation index was derived by applying the MRI signal equation to phantom-calibrated coregistered FMX-enhanced MRI brain scans acquired before, 1-4 hours after, and 16-24 hours after FMX administration. The fraction of voxels with an FMX compartmentation index greater than 1 was computed over the whole tumor (FCIGT1) and from voxels above the 90th percentile R* (FCIGT1 R*). Results rR* computed from pretherapy MRI performed 16-24 hours after FMX administration, without reference to calibration phantoms, predicted response to nal-IRI in thoracoabdominal metastases (accuracy, 74%). rR* performance was robust to the inclusion of some peritumoral tissue within the tumor region of interest. FCIGT1 R* provided 79% accuracy on cross-validation in prediction of response in brain metastases. Conclusion This first in-human study focused on mBC suggests that FMX-enhanced MRI biologic markers can be useful for pretherapy prediction of response to nal-IRI in patients with mBC. MRI Contrast Agent, MRI, Breast, Head/Neck, Tumor Response, Experimental Investigations, Brain/Brain Stem Clinical trial registration no. NCT01770353 © RSNA, 2023 See also commentary by Daldrup-Link in this issue.

摘要

目的 研究 Ferumoxytol(FMX)增强 MRI 作为预测转移性乳腺癌(mBC)患者胸腹部和脑转移接受脂质体伊立替康(nal-IRI)治疗反应的预处理指标的价值。

材料与方法 在这项 1 期扩展试验(ClinicalTrials.gov 标识符:NCT01770353;27 名参与者)中,分析了 49 个胸腹部(19 名参与者;平均年龄 48 岁±11[标准差])和 19 个脑(7 名参与者;平均年龄 54 岁±8)转移灶的 MRI 图像,这些图像在 FMX 给药前、给药后 1-4 小时和 16-24 小时采集。在胸腹部转移灶中,肿瘤横向弛豫率(R*)与脾脏的平均 R*(rR*)进行归一化,计算 rR的肿瘤直方图指标 rR,表示体素中 rR高于第 th 百分位数的平均值。在脑转移灶中,通过应用 MRI 信号方程,对给药前、给药后 1-4 小时和 16-24 小时采集的经过 FMX 校准的配准 FMX 增强 MRI 脑扫描进行处理,得到一个新的分区指数。计算整个肿瘤(FCIGT1)和高于 rR第 90 百分位数的体素(FCIGT1 R*)的 FMX 分区指数大于 1 的体素分数。

结果 在 FMX 给药后 16-24 小时采集的治疗前 MRI 上计算 rR*,无需参考校准体模,可预测胸腹部转移灶对 nal-IRI 的反应(准确率为 74%)。rR* 的性能在纳入肿瘤感兴趣区周围的一些肿瘤组织时具有稳健性。FCIGT1 R*在脑转移灶反应预测的交叉验证中准确率为 79%。

结论 这项针对 mBC 的首次人体研究表明,FMX 增强 MRI 生物标志物可用于预测 mBC 患者接受 nal-IRI 治疗的反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c19d/10077095/ad40ba2cb9c3/rycan.220022.VA.jpg

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