Belykh Evgenii, Bardonova Liudmila, Abramov Irakliy, Byvaltsev Vadim A, Kerymbayev Talgat, Yu Kwanha, Healey Debbie R, Luna-Melendez Ernesto, Deneen Benjamin, Mehta Shwetal, Liu James K, 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, New Jersey Medical School, Rutgers University, Newark, NJ, United States.
Front Oncol. 2023 May 23;13:1156812. doi: 10.3389/fonc.2023.1156812. eCollection 2023.
Surgical resection remains the first-line treatment for gliomas. Several fluorescent dyes are currently in use to augment intraoperative tumor visualization, but information on their comparative effectiveness is lacking. We performed systematic assessment of fluorescein sodium (FNa), 5-aminolevulinic acid (5-ALA)-induced protoporphyrin IX (PpIX), and indocyanine green (ICG) fluorescence in various glioma models using advanced fluorescence imaging techniques.
Four glioma models were used: GL261 (high-grade model), GB3 (low-grade model), and an electroporation model with and without red fluorescence protein (IUE +RFP and IUE -RFP, respectively) (intermediate-to-low-grade model). Animals underwent 5-ALA, FNa, and ICG injections and craniectomy. Brain tissue samples underwent fluorescent imaging using a wide-field operative microscope and a benchtop confocal microscope and were submitted for histologic analysis.
Our systematic analysis showed that wide-field imaging of highly malignant gliomas is equally efficient with 5-ALA, FNa, and ICG, although FNa is associated with more false-positive staining of the normal brain. In low-grade gliomas, wide-field imaging cannot detect ICG staining, can detect FNa in only 50% of specimens, and is not sensitive enough for PpIX detection. With confocal imaging of low-intermediate grade glioma models, PpIX outperformed FNa.
Overall, compared to wide-field imaging, confocal microscopy significantly improved diagnostic accuracy and was better at detecting low concentrations of PpIX and FNa, resulting in improved tumor delineation. Neither PpIX, FNa, nor ICG delineated all tumor boundaries in studied tumor models, which emphasizes the need for novel visualization technologies and molecular probes to guide glioma resection. Simultaneous administration of 5-ALA and FNa with use of cellular-resolution imaging modalities may provide additional information for margin detection and may facilitate maximal glioma resection.
手术切除仍然是胶质瘤的一线治疗方法。目前有几种荧光染料用于增强术中肿瘤可视化,但缺乏关于它们相对有效性的信息。我们使用先进的荧光成像技术,对各种胶质瘤模型中的荧光素钠(FNa)、5-氨基乙酰丙酸(5-ALA)诱导的原卟啉IX(PpIX)和吲哚菁绿(ICG)荧光进行了系统评估。
使用了四种胶质瘤模型:GL261(高级别模型)、GB3(低级别模型)以及带有和不带有红色荧光蛋白的电穿孔模型(分别为IUE +RFP和IUE -RFP,中低级别模型)。动物接受5-ALA、FNa和ICG注射以及开颅手术。脑组织样本使用宽视野手术显微镜和台式共聚焦显微镜进行荧光成像,并提交进行组织学分析。
我们的系统分析表明,对于高度恶性胶质瘤的宽视野成像,5-ALA、FNa和ICG同样有效,尽管FNa与正常脑的假阳性染色更多相关。在低级别胶质瘤中,宽视野成像无法检测到ICG染色,仅在50%的标本中能检测到FNa,对PpIX检测不够敏感。在中低级别胶质瘤模型的共聚焦成像中,PpIX优于FNa。
总体而言,与宽视野成像相比,共聚焦显微镜显著提高了诊断准确性,并且在检测低浓度的PpIX和FNa方面表现更好,从而改善了肿瘤边界的勾勒。在研究的肿瘤模型中,PpIX、FNa和ICG均未勾勒出所有肿瘤边界,这强调了需要新的可视化技术和分子探针来指导胶质瘤切除。同时给予5-ALA和FNa并使用细胞分辨率成像模式可能为切缘检测提供额外信息,并可能有助于最大程度地切除胶质瘤。