Cho Steve Y, Lipson Evan J, Im Hyung-Jun, Rowe Steven P, Gonzalez Esther Mena, Blackford Amanda, Chirindel Alin, Pardoll Drew M, Topalian Suzanne L, Wahl Richard L
Johns Hopkins University School of Medicine and Sidney Kimmel Comprehensive Cancer Center, Baltimore, Maryland
University of Wisconsin School of Medicine and Public Health and Carbone Comprehensive Cancer Center, Madison, Wisconsin.
J Nucl Med. 2017 Sep;58(9):1421-1428. doi: 10.2967/jnumed.116.188839. Epub 2017 Mar 30.
The purpose of this study was to evaluate F-FDG PET/CT scanning as an early predictor of response to immune checkpoint inhibitors (ICIs) in patients with advanced melanoma. Twenty patients with advanced melanoma receiving ICI prospectively underwent F-FDG PET/CT at 3 scan intervals: before treatment initiation (SCAN-1), at days 21-28 (SCAN-2), and at 4 mo (SCAN-3). This study was approved by the institutional review board, and informed consent was received from all patients who were enrolled between April 2012 and December 2013. Tumor response at each posttreatment time point was assessed according to RECIST 1.1, immune-related response criteria, PERCIST (PERCIST 1.0), and European Organization for Research and Treatment of Cancer (EORTC) criteria. Performance characteristics of each metric to predict best overall response (BOR) at ≥ 4 mo were assessed. Twenty evaluable patients were treated with ipilimumab ( = 16), BMS-936559 ( = 3), or nivolumab ( = 1). BOR at ≥ 4 mo included complete response ( = 2), partial response ( = 2), stable disease ( = 1), and progressive disease ( = 15). Response evaluations at SCAN-2 using RECIST 1.1, immune-related response criteria, PERCIST, and EORTC criteria demonstrated accuracies of 75%, 70%, 70%, and 65%, respectively, to predict BOR at ≥ 4 mo. Interestingly, the optimal PERCIST and EORTC threshold values at SCAN-2 to predict BOR were >15.5% and >14.7%, respectively. By combining anatomic and functional imaging data collected at SCAN-2, we developed criteria to predict eventual response to ICI with 100% sensitivity, 93% specificity, and 95% accuracy. Combining functional and anatomic imaging parameters from F-FDG PET/CT scans performed early in ICI appears predictive for eventual response in patients with advanced melanoma. These findings require validation in larger cohorts.
本研究的目的是评估F-FDG PET/CT扫描作为晚期黑色素瘤患者对免疫检查点抑制剂(ICI)反应的早期预测指标。20例接受ICI治疗的晚期黑色素瘤患者在3个扫描时间点前瞻性地接受了F-FDG PET/CT检查:治疗开始前(扫描-1)、第21 - 28天(扫描-2)和4个月时(扫描-3)。本研究经机构审查委员会批准,并获得了2012年4月至2013年12月期间所有入组患者的知情同意书。根据RECIST 1.1、免疫相关反应标准、PERCIST(PERCIST 1.0)和欧洲癌症研究与治疗组织(EORTC)标准评估每个治疗后时间点的肿瘤反应。评估了每个指标预测≥4个月时最佳总体反应(BOR)的性能特征。20例可评估患者接受了伊匹单抗(n = 16)、BMS-936559(n = 3)或纳武单抗(n = 1)治疗。≥4个月时的BOR包括完全缓解(n = 2)、部分缓解(n = 2)、疾病稳定(n = 1)和疾病进展(n = 15)。使用RECIST 1.1、免疫相关反应标准、PERCIST和EORTC标准在扫描-2时进行的反应评估显示,预测≥4个月时BOR的准确率分别为75%、70%、70%和65%。有趣的是,扫描-2时预测BOR的最佳PERCIST和EORTC阈值分别>15.5%和>14.7%。通过结合在扫描-2时收集的解剖学和功能成像数据,我们制定了预测ICI最终反应的标准,其敏感性为100%,特异性为93%,准确性为95%。结合ICI早期进行的F-FDG PET/CT扫描的功能和解剖成像参数似乎可预测晚期黑色素瘤患者的最终反应。这些发现需要在更大的队列中进行验证。