Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Department of Neurosurgery, Hospital of the University of Pennsylvania, Philadelphia, PA, USA.
Mol Imaging Biol. 2020 Oct;22(5):1427-1437. doi: 10.1007/s11307-019-01455-x.
Intraoperative molecular imaging with tumor-targeting fluorophores offers real-time detection of neoplastic tissue. The second window indocyanine green (SWIG) technique relies on passive accumulation of indocyanine green (ICG), a near-infrared fluorophore, in neoplastic tissues. In this study, we explore the ability of SWIG to detect neoplastic tissue and to predict postoperative magnetic resonance imaging (MRI) findings intraoperatively.
Retrospective data were collected from 36 patients with primary high-grade gliomas (HGG) enrolled as part of a larger trial between October 2014 and October 2018. Patients received systemic ICG infusions at 2.5-5 mg/kg 24 h preoperatively. Near-infrared fluorescence was recorded throughout the case and from biopsy specimens. The presence/location of residual SWIG signal after resection was compared to the presence/location of residual gadolinium enhancement on postoperative MRI. The extent of resection was not changed based on near-infrared imaging.
All 36 lesions demonstrated strong near-infrared fluorescence (signal-to-background = 6.8 ± 2.2) and 100 % of tumors reaching the cortex were visualized before durotomy. In 78 biopsy specimens, near-infrared imaging demonstrated higher sensitivity and accuracy than white light for diagnosing neoplastic tissue intraoperatively. Furthermore, near-infrared imaging predicted gadolinium enhancement on postoperative MRI with 91 % accuracy, with visualization of residual enhancement as small as 0.3 cm. Patients with no residual near-infrared signal after resection were significantly more likely to have complete resection on postoperative MRI (p value < 0.0001).
Intraoperative imaging with SWIG demonstrates highly sensitive detection of HGG tissue in real time. Furthermore, post-resection near-infrared imaging correlates with postoperative MRI. Overall, our findings suggest that SWIG can provide surgeons with MRI-like results in real time, potentially increasing resection rates.
术中使用靶向荧光染料进行分子成像可实时检测肿瘤组织。第二窗口近红外吲哚菁绿(SWIG)技术依赖于近红外荧光染料吲哚菁绿(ICG)在肿瘤组织中的被动积累。在这项研究中,我们探索了 SWIG 检测肿瘤组织的能力,并在术中预测术后磁共振成像(MRI)结果。
回顾性收集了 2014 年 10 月至 2018 年 10 月期间参加更大规模试验的 36 名原发性高级别神经胶质瘤(HGG)患者的数据。患者在术前 24 小时内以 2.5-5mg/kg 的剂量接受全身 ICG 输注。整个手术过程中及活检标本中均记录近红外荧光。切除后残余 SWIG 信号的存在/位置与术后 MRI 上残余钆增强的存在/位置进行比较。切除范围不根据近红外成像进行改变。
所有 36 个病变均显示强烈的近红外荧光(信号背景比=6.8±2.2),并且在切开硬脑膜之前,100%的肿瘤到达皮质。在 78 个活检标本中,近红外成像在术中诊断肿瘤组织方面的敏感性和准确性均高于白光。此外,近红外成像以 91%的准确率预测术后 MRI 的钆增强,对小至 0.3cm 的残余增强均能进行可视化。切除后无残余近红外信号的患者在术后 MRI 上有更大可能实现完全切除(p 值<0.0001)。
SWIG 术中成像可实时灵敏地检测 HGG 组织。此外,切除后近红外成像与术后 MRI 相关。总体而言,我们的研究结果表明,SWIG 可实时为外科医生提供类似 MRI 的结果,可能提高切除率。