Hadjipanayis Costas G, Widhalm Georg, Stummer Walter
*Department of Neurosurgery, Icahn School of Medicine at Mount Sinai, New York, NY; ‡Department of Neurosurgery, Medical University Vienna, Vienna, Austria; §Department of Neurosurgery, University of Munster, Munster, Germany.
Neurosurgery. 2015 Nov;77(5):663-73. doi: 10.1227/NEU.0000000000000929.
The current neurosurgical goal for patients with malignant gliomas is maximal safe resection of the contrast-enhancing tumor. However, a complete resection of the contrast-enhancing tumor is achieved only in a minority of patients. One reason for this limitation is the difficulty in distinguishing viable tumor from normal adjacent brain during surgery at the tumor margin using conventional white-light microscopy. To overcome this limitation, fluorescence-guided surgery (FGS) using 5-aminolevulinic acid (5-ALA) has been introduced in the treatment of malignant gliomas. FGS permits the intraoperative visualization of malignant glioma tissue and supports the neurosurgeon with real-time guidance for differentiating tumor from normal brain that is independent of neuronavigation and brain shift. Tissue fluorescence after oral administration of 5-ALA is associated with unprecedented high sensitivity, specificity, and positive predictive values for identifying malignant glioma tumor tissue. 5-ALA-induced tumor fluorescence in diffusely infiltrating gliomas with non-significant magnetic resonance imaging contrast-enhancement permits intraoperative identification of anaplastic foci and establishment of an accurate histopathological diagnosis for proper adjuvant treatment. 5-ALA FGS has enabled surgeons to achieve a significantly higher rate of complete resections of malignant gliomas in comparison with conventional white-light resections. Consequently, 5-ALA FGS has become an indispensable surgical technique and standard of care at many neurosurgical departments around the world. We conducted an extensive literature review concerning the surgical benefit of using 5-ALA for FGS of malignant gliomas. According to the literature, there are a number of reasons for the neurosurgeon to perform 5-ALA FGS, which will be discussed in detail in the current review.
目前,恶性胶质瘤患者的神经外科手术目标是最大程度安全切除增强显影的肿瘤。然而,只有少数患者能够实现增强显影肿瘤的完全切除。造成这一限制的一个原因是,在手术中使用传统白光显微镜在肿瘤边缘区分存活肿瘤与相邻正常脑组织存在困难。为克服这一限制,已将使用5-氨基酮戊酸(5-ALA)的荧光引导手术(FGS)引入恶性胶质瘤的治疗中。FGS可实现术中对恶性胶质瘤组织的可视化,并为神经外科医生提供实时指导,以区分肿瘤与正常脑组织,且不受神经导航和脑移位的影响。口服5-ALA后的组织荧光对于识别恶性胶质瘤肿瘤组织具有前所未有的高灵敏度、特异性和阳性预测值。在磁共振成像增强不显著的弥漫性浸润性胶质瘤中,5-ALA诱导的肿瘤荧光可实现术中识别间变灶,并建立准确的组织病理学诊断以进行适当的辅助治疗。与传统白光切除术相比,5-ALA FGS使外科医生能够显著提高恶性胶质瘤的完全切除率。因此,5-ALA FGS已成为世界上许多神经外科科室不可或缺的手术技术和治疗标准。我们对使用5-ALA进行恶性胶质瘤FGS的手术益处进行了广泛的文献综述。根据文献,神经外科医生进行5-ALA FGS有多种原因,将在本综述中详细讨论。