Xu Yuan, On Thomas J, Abramov Irakliy, Alcantar-Garibay Oscar, Hartke Joelle N, Eschbacher Jennifer M, Yangi Kivanc, Lawton Michael T, Smith Kris A, Porter Randall W, Preul Mark C
The Loyal and Edith Davis Neurosurgical Research Laboratory, Department of Neurosurgery, Barrow Neurological Institute, St. Joseph's Hospital and Medical Center, Phoenix, AZ, United States.
Department of Neurosurgery, Barrow Neurological Institute, St. Joseph's Hospital and Medical Center, Phoenix, AZ, United States.
Front Oncol. 2025 May 14;15:1565935. doi: 10.3389/fonc.2025.1565935. eCollection 2025.
Confocal laser endomicroscopy (CLE), a handheld imaging technology, provides intraoperative real-time cellular resolution examination of tissue architecture. We evaluated the feasibility and diagnostic capability of the first clinically approved CLE system for intraoperative imaging of brain tumors.
A total of 50 patients who were to undergo brain tumor surgery were prospectively enrolled. CLE images were interpreted by one CLE-experienced neuropathologist as lesional, non-lesional, or non-interpretable and compared to tissue histology acquired at the same location under neuronavigation. Diagnostic accuracy of CLE imaging was calculated using permanent sections as the standard for comparison. The neuropathologist provided real-time image interpretation using a built-in telepathology consultation platform in 27 cases.
The final pathology of the tumors in these patients included 28 gliomas, 5 meningiomas, 3 metastatic brain tumors, 5 treatment-related changes, and 10 other primary intracranial tumors. A total of 13,535 interpretable images were acquired from 304 regions of interest (ROIs). The first informative images were acquired within 10.5 s after the initiation of CLE imaging for each ROI. Mean CLE imaging time per case was 8.6 min. Using telepathology consultation extended CLE imaging per case time by 3.8 min (p=0.005). Communication between neurosurgeon and neuropathologist lasted 3.9 min per ROI. Overall sensitivity and specificity of CLE imaging were 93% and 81%, respectively. The specificity differed significantly between core and margin ROIs in glioma cases (93% vs. 50%, p=0.039). Diagnostic performance was not statistically different between new and recurrent glioma cases or between glioma and other tumor types.
The clinically approved CLE system allows intraoperative visualization of tissue histoarchitecture and identification of lesional tissue in real time, without the need for tissue biopsy and processing. CLE is efficient and cost-effective, with high diagnostic accuracy at the glioma core. However, CLE imaging at the tumor margin remains challenging.
共聚焦激光内镜显微镜(CLE)是一种手持式成像技术,可在术中对组织结构进行实时细胞分辨率检查。我们评估了首个获得临床批准的用于脑肿瘤术中成像的CLE系统的可行性和诊断能力。
前瞻性纳入50例拟行脑肿瘤手术的患者。由一位有CLE经验的神经病理学家将CLE图像解读为病变、非病变或不可解读,并与在神经导航下同一位置获取的组织病理学进行比较。以永久切片作为比较标准计算CLE成像的诊断准确性。这位神经病理学家在27例病例中使用内置的远程病理学会诊平台提供实时图像解读。
这些患者肿瘤的最终病理结果包括28例胶质瘤、5例脑膜瘤、3例脑转移瘤、5例治疗相关改变和10例其他原发性颅内肿瘤。从304个感兴趣区域(ROI)共获取了13535张可解读图像。每个ROI在CLE成像开始后10.5秒内获得首张信息性图像。每例患者的平均CLE成像时间为8.6分钟。使用远程病理学会诊使每例患者的CLE成像时间延长了3.8分钟(p=0.005)。神经外科医生和神经病理学家之间的沟通每个ROI持续3.9分钟。CLE成像的总体敏感性和特异性分别为93%和81%。在胶质瘤病例中,核心ROI和边缘ROI的特异性差异显著(93%对50%,p=0.039)。新诊断和复发的胶质瘤病例之间或胶质瘤与其他肿瘤类型之间的诊断性能在统计学上无差异。
获得临床批准的CLE系统可在术中实时可视化组织组织结构并识别病变组织,无需进行组织活检和处理。CLE高效且具有成本效益,在胶质瘤核心部位具有较高的诊断准确性。然而,肿瘤边缘的CLE成像仍然具有挑战性。