Gerwing Mirjam, Krähling Tobias, Schliemann Christoph, Harrach Saliha, Schwöppe Christian, Berdel Andrew F, Klein Sebastian, Hartmann Wolfgang, Wardelmann Eva, Heindel Walter L, Lenz Georg, Berdel Wolfgang E, Wildgruber Moritz
Clinic of Radiology, University Hospital Muenster, D-48149 Muenster, Germany.
Department of Medicine A, Hematology, Hemostaseology, Oncology and Pulmonology, University Hospital Muenster, D-48149 Muenster, Germany.
Cancers (Basel). 2021 Nov 23;13(23):5880. doi: 10.3390/cancers13235880.
Early assessment of target hit in anti-cancer therapies is a major task in oncologic imaging. In this study, immediate target hit and effectiveness of CD13-targeted tissue factor tTF-NGR in patients with advanced malignant disease enrolled in a phase I trial was assessed using a multiparametric MRI protocol. Seventeen patients with advanced solid malignancies were enrolled in the trial and received tTF-NGR for at least one cycle of five daily infusions. Tumor target lesions were imaged with multiparametric MRI before therapy initiation, five hours after the first infusion and after five days. The imaging protocol comprised ADC, calculated from DWI, and DCE imaging and vascular volume fraction (VVF) assessment. DCE and VVF values decreased within 5 h after therapy initiation, indicating early target hit with a subsequent decrease in tumor perfusion due to selective tumor vessel occlusion and thrombosis induced by tTF-NGR. Simultaneously, ADC values increased at five hours after tTF-NGR administration. In four patients, treatment had to be stopped due to an increase in troponin T hs, with subsequent anticoagulation. In these patients, a reversed effect, with DCE and VVF values increasing and ADC values decreasing, was observed after anticoagulation. Changes in imaging parameters were independent of the mean vessel density determined by immunohistochemistry. By using a multiparametric imaging approach, changes in tumor perfusion after initiation of a tumor vessel occluding therapy can be evaluated as early as five hours after therapy initiation, enabling early assessment of target hit.
抗癌治疗中靶点命中的早期评估是肿瘤影像学的一项主要任务。在本研究中,使用多参数MRI方案评估了参与I期试验的晚期恶性疾病患者中CD13靶向组织因子tTF-NGR的即时靶点命中情况和有效性。17例晚期实体恶性肿瘤患者入组该试验,接受tTF-NGR治疗至少一个周期,每日输注5次。在治疗开始前、首次输注后5小时和5天后,用多参数MRI对肿瘤靶病变进行成像。成像方案包括根据扩散加权成像(DWI)计算的表观扩散系数(ADC)、动态对比增强(DCE)成像和血管容积分数(VVF)评估。治疗开始后5小时内,DCE和VVF值下降,表明早期靶点命中,随后由于tTF-NGR诱导的选择性肿瘤血管闭塞和血栓形成,肿瘤灌注减少。同时,tTF-NGR给药后5小时ADC值升高。4例患者因肌钙蛋白T hs升高而不得不停止治疗,随后进行抗凝治疗。在这些患者中,抗凝治疗后观察到相反的效果,即DCE和VVF值升高,ADC值降低。成像参数的变化与免疫组化测定的平均血管密度无关。通过使用多参数成像方法,在肿瘤血管闭塞治疗开始后5小时即可评估肿瘤灌注的变化,从而能够早期评估靶点命中情况。