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