Indocyanine-Green for Fluorescence-Guided Surgery of Brain Tumors: Evidence, Techniques, and Practical Experience

The primary treatment for brain tumors often involves surgical resection for diagnosis, relief of mass effect, and prolonged survival. In neurosurgery, it is of utmost importance to achieve maximal safe resection while minimizing iatrogenic neurologic deficit. Thus, neurosurgeons often rely on extra tools in the operating room, such as neuronavigation, intraoperative magnetic resonance imaging, and/or intraoperative rapid pathology. However, these tools can be expensive, not readily available, time-consuming, and/or inaccurate. Recently, fluorescence-guided surgery has emerged as a cost-effective method to accurately visualize neoplastic areas in real-time to guide resection. Currently, 5-aminolevulinic-acid (5-ALA) remains the only fluorophore that has been approved specifically for fluorescence-guided tumor resection. Its use has demonstrated improved resection rates and prolonged progression-free survival. However, protoporphyrin-IX, the metabolic product of 5-ALA that accumulates in neoplastic cells, fluoresces in the visible-light range, which suffers from limited tissue penetration and significant auto-fluorescence. Near-infrared fluorescence, on the other hand, overcomes these problems with ease. Since 2012, researchers at our institution have developed a novel technique using indocyanine-green, which is a well-known near-infrared fluorophore used traditionally for angiography. This Second-Window-ICG (SWIG) technique takes advantage of the increased endothelial permeability in peritumoral tissue, which allows indocyanine-green to accumulate in these areas for intraoperative visualization of the tumor. SWIG has demonstrated utility in gliomas, meningiomas, metastases, pituitary adenomas, chordomas, and craniopharyngiomas. The main benefits of SWIG stem from its highly sensitive detection of neoplastic tissue in a wide variety of intracranial pathologies in real-time, which can help neurosurgeons both during surgical resections and in stereotactic biopsies. In this review of this novel technique, we summarize the development and mechanism of action of SWIG, provide evidence for its benefits, and discuss its limitations. Finally, for those interested in near-infrared fluorescence-guided surgery, we provide suggestions for maximizing the benefits while minimizing the limitations of SWIG based on our own experience thus far.

[1]  W. Paiva,et al.  Natural history of intraventricular meningiomas: systematic review , 2018, Neurosurgical Review.

[2]  Mitchel S Berger,et al.  An extent of resection threshold for newly diagnosed glioblastomas. , 2011, Journal of neurosurgery.

[3]  N. Oyesiku,et al.  Congress of Neurological Surgeons Systematic Review and Evidence-Based Guideline on Surgical Techniques and Technologies for the Management of Patients With Nonfunctioning Pituitary Adenomas. , 2016, Neurosurgery.

[4]  John Y. K. Lee,et al.  Contemporary neurosurgical techniques for pituitary tumor resection , 2014, Journal of Neuro-Oncology.

[5]  J. Frangioni In vivo near-infrared fluorescence imaging. , 2003, Current opinion in chemical biology.

[6]  H Stepp,et al.  Intraoperative detection of malignant gliomas by 5-aminolevulinic acid-induced porphyrin fluorescence. , 1998, Neurosurgery.

[7]  D. Simpson THE RECURRENCE OF INTRACRANIAL MENINGIOMAS AFTER SURGICAL TREATMENT , 1957, Journal of neurology, neurosurgery, and psychiatry.

[8]  Ahmed El-Henawy,et al.  A comparative Analytical Studies onAcaciapolyacantha gum Samples collected from three different locations in Sudan , 2014 .

[9]  Johan Moan,et al.  On the selectivity of 5-aminolevulinic acid-induced protoporphyrin IX formation. , 2004, Current medicinal chemistry. Anti-cancer agents.

[10]  Ollin G Venegas,et al.  Optimization of the enhanced permeability and retention effect for near-infrared imaging of solid tumors with indocyanine green. , 2015, American journal of nuclear medicine and molecular imaging.

[11]  Francesco Acerbi,et al.  Is fluorescein-guided technique able to help in resection of high-grade gliomas? , 2014, Neurosurgical focus.

[12]  P. Bonney,et al.  Outcomes following transsphenoidal surgical management of incidental pituitary adenomas: a series of 52 patients over a 17-year period. , 2019, Journal of neurosurgery.

[13]  Peter Nakaji,et al.  Diagnostic Accuracy of a Confocal Laser Endomicroscope for In Vivo Differentiation Between Normal Injured And Tumor Tissue During Fluorescein-Guided Glioma Resection: Laboratory Investigation. , 2018, World neurosurgery.

[14]  W. Stummer,et al.  Kinetics of porphyrin fluorescence accumulation in pediatric brain tumor cells incubated in 5-aminolevulinic acid , 2014, Acta Neurochirurgica.

[15]  Roy A Patchell,et al.  The management of brain metastases. , 2003, Cancer treatment reviews.

[16]  P. Eldridge,et al.  Long-term survival analysis of atypical meningiomas: survival rates, prognostic factors, operative and radiotherapy treatment , 2014, Acta Neurochirurgica.

[17]  Z L Gokaslan,et al.  A multivariate analysis of 416 patients with glioblastoma multiforme: prognosis, extent of resection, and survival. , 2001, Journal of neurosurgery.

[18]  M M Haglund,et al.  Enhanced optical imaging of human gliomas and tumor margins. , 1996, Neurosurgery.

[19]  J. Fandino,et al.  Intraoperative 5-aminolevulinic-acid-induced fluorescence in meningiomas , 2010, Acta Neurochirurgica.

[20]  H. Maeda,et al.  Tumor vascular permeability and the EPR effect in macromolecular therapeutics: a review. , 2000, Journal of controlled release : official journal of the Controlled Release Society.

[21]  N. Pleshko,et al.  Wavelength-dependent penetration depth of near infrared radiation into cartilage. , 2015, The Analyst.

[22]  R. Mekary,et al.  Gross total resection of pituitary adenomas after endoscopic vs. microscopic transsphenoidal surgery: a meta-analysis , 2018, Acta Neurochirurgica.

[23]  Shuming Nie,et al.  Near-infrared fluorescent image-guided surgery for intracranial meningioma. , 2017, Journal of neurosurgery.

[24]  D. A. Hansen,et al.  Indocyanine green (ICG) staining and demarcation of tumor margins in a rat glioma model. , 1993, Surgical neurology.

[25]  F. Schmidt Meta-Analysis , 2008 .

[26]  Kathleen Seidel,et al.  Gross total resection rates in contemporary glioblastoma surgery: results of an institutional protocol combining 5-aminolevulinic acid intraoperative fluorescence imaging and brain mapping. , 2012, Neurosurgery.

[27]  Z. Ram,et al.  Treatment of clinically nonfunctioning pituitary adenomas with dopamine agonists. , 2016, European journal of endocrinology.

[28]  Brian W Pogue,et al.  Review of fluorescence guided surgery systems: identification of key performance capabilities beyond indocyanine green imaging , 2016, Journal of biomedical optics.

[29]  John Y. K. Lee,et al.  Comparison of Near-Infrared Imaging Camera Systems for Intracranial Tumor Detection , 2018, Molecular Imaging and Biology.

[30]  John Y. K. Lee,et al.  Folate receptor overexpression can be visualized in real time during pituitary adenoma endoscopic transsphenoidal surgery with near-infrared imaging. , 2017, Journal of neurosurgery.

[31]  Guangming Wang,et al.  Gross Total Resection of Glioma with the Intraoperative Fluorescence-guidance of Fluorescein Sodium , 2012, International journal of medical sciences.

[32]  Frederic Leblond,et al.  5-Aminolevulinic Acid-Induced Protoporphyrin IX Fluorescence in Meningioma: Qualitative and Quantitative Measurements In Vivo , 2014, Neurosurgery.

[33]  C. Nimsky,et al.  Follow-up and long-term outcome of nonfunctioning pituitary adenoma operated by transsphenoidal surgery with intraoperative high-field magnetic resonance imaging , 2014, Acta Neurochirurgica.

[34]  Sunil Singhal,et al.  Intraoperative near-infrared imaging with receptor-specific versus passive delivery of fluorescent agents in pituitary adenomas. , 2019, Journal of neurosurgery.

[35]  Changhong Shi,et al.  The Application of Heptamethine Cyanine Dye DZ-1 and Indocyanine Green for Imaging and Targeting in Xenograft Models of Hepatocellular Carcinoma , 2017, International journal of molecular sciences.

[36]  P. L. Le Roux,et al.  Race against the clock: overcoming challenges in the management of anticoagulant-associated intracerebral hemorrhage. , 2014, Journal of neurosurgery.

[37]  Sunil Singhal,et al.  Intraoperative Near-Infrared Optical Imaging Can Localize Gadolinium-Enhancing Gliomas During Surgery. , 2016, Neurosurgery.

[38]  Shuming Nie,et al.  Intraoperative Near-Infrared Imaging Can Distinguish Cancer from Normal Tissue but Not Inflammation , 2014, PloS one.

[39]  John Y. K. Lee,et al.  Folate Receptor Overexpression in Human and Canine Meningiomas-Immunohistochemistry and Case Report of Intraoperative Molecular Imaging. , 2018, Neurosurgery.

[40]  S. Anai,et al.  Expression of ferrochelatase has a strong correlation in protoporphyrin IX accumulation with photodynamic detection of bladder cancer. , 2016, Photodiagnosis and photodynamic therapy.

[41]  J. Bruce,et al.  The feasibility of real-time in vivo optical detection of blood–brain barrier disruption with indocyanine green , 2012, Journal of Neuro-Oncology.

[42]  Alessandro Villa,et al.  Fluorescein for resection of high-grade gliomas: A safety study control in a single center and review of the literature , 2017, Surgical neurology international.

[43]  M. Knauth,et al.  The benefit of neuronavigation for neurosurgery analyzed by its impact on glioblastoma surgery , 2000, Neurological research.

[44]  M M Haglund,et al.  Enhanced optical imaging of rat gliomas and tumor margins. , 1994, Neurosurgery.

[45]  Y. Adachi,et al.  Neurotransmitter Transporter Family Including SLC6A6 and SLC6A13 Contributes to the 5‐Aminolevulinic Acid (ALA)‐Induced Accumulation of Protoporphyrin IX and Photodamage, through Uptake of ALA by Cancerous Cells , 2014, Photochemistry and photobiology.

[46]  Sunil Singhal,et al.  Near-Infrared Optical Contrast of Skull Base Tumors During Endoscopic Endonasal Surgery. , 2018, Operative neurosurgery.

[47]  C. Nimsky,et al.  Intraoperative high-field MRI for transsphenoidal reoperations of nonfunctioning pituitary adenoma. , 2014, Journal of Neurosurgery.

[48]  A. Kato,et al.  Fluorescence-guided surgery for glioblastoma multiforme using high-dose fluorescein sodium with excitation and barrier filters , 2012, Journal of Clinical Neuroscience.

[49]  M. Sam Eljamel,et al.  Intraoperative optical identification of pituitary adenomas , 2009, Journal of Neuro-Oncology.

[50]  Walter Stummer,et al.  The importance of surgical resection in malignant glioma , 2009, Current opinion in neurology.

[51]  Guy M. McKhann,et al.  Sodium Fluorescein Facilitates Guided Sampling of Diagnostic Tumor Tissue in Nonenhancing Gliomas , 2018, Neurosurgery.

[52]  John Y. K. Lee,et al.  Folate Receptor Near-Infrared Optical Imaging Provides Sensitive and Specific Intraoperative Visualization of Nonfunctional Pituitary Adenomas. , 2019, Operative neurosurgery.

[53]  F. Zanella,et al.  Fluorescence-guided surgery with 5-aminolevulinic acid for resection of malignant glioma: a randomised controlled multicentre phase III trial. , 2006, The Lancet. Oncology.

[54]  W. Stummer,et al.  Randomized, Prospective Double-Blinded Study Comparing 3 Different Doses of 5-Aminolevulinic Acid for Fluorescence-Guided Resections of Malignant Gliomas , 2017, Neurosurgery.

[55]  R. C. Macridis A review , 1963 .

[56]  R. Beroukhim,et al.  Extent of resection and overall survival for patients with atypical and malignant meningioma , 2015, Cancer.

[57]  A. Kato,et al.  Fluorescence-guided surgery of metastatic brain tumors using fluorescein sodium , 2010, Journal of Clinical Neuroscience.

[58]  Sunil Singhal,et al.  The second window ICG technique demonstrates a broad plateau period for near infrared fluorescence tumor contrast in glioblastoma , 2017, PloS one.

[59]  Shuming Nie,et al.  Intraoperative Near-Infrared Optical Contrast Can Localize Brain Metastases. , 2017, World neurosurgery.

[60]  Xiaoyao Fan,et al.  Red-light excitation of protoporphyrin IX fluorescence for subsurface tumor detection. , 2017, Journal of neurosurgery.

[61]  W. Stummer,et al.  Dual-labeling with 5-aminolevulinic acid and fluorescein for fluorescence-guided resection of high-grade gliomas: technical note. , 2017, Journal of neurosurgery.

[62]  Shereen Ezzat,et al.  The prevalence of pituitary adenomas , 2004, Cancer.

[63]  E. Mohammadi,et al.  Barriers and facilitators related to the implementation of a physiological track and trigger system: A systematic review of the qualitative evidence , 2017, International journal for quality in health care : journal of the International Society for Quality in Health Care.

[64]  Peter Nakaji,et al.  Use of in vivo near-infrared laser confocal endomicroscopy with indocyanine green to detect the boundary of infiltrative tumor. , 2011, Journal of neurosurgery.

[65]  J. Willerson,et al.  LABORATORY INVESTIGATION , 2005 .

[66]  Andrzej Galat,et al.  Technical note , 2008, Comput. Biol. Chem..

[67]  Shuming Nie,et al.  Intraoperative Near-Infrared Imaging of Surgical Wounds after Tumor Resections Can Detect Residual Disease , 2012, Clinical Cancer Research.

[68]  Dieter Jahn,et al.  Structure and function of enzymes in heme biosynthesis , 2010, Protein science : a publication of the Protein Society.

[69]  M. K. Hamamcıoğlu,et al.  Use of Sodium Fluorescein in Meningioma Surgery Performed Under the YELLOW-560 nm Surgical Microscope Filter: Feasibility and Preliminary Results. , 2017, World neurosurgery.

[70]  Ricardo J Komotar,et al.  Neurosurgery for Brain Tumors: Update on Recent Technical Advances , 2011, Current neurology and neuroscience reports.

[71]  Cheng-Chia Lee,et al.  Congress of Neurological Surgeons Systematic Review and Evidence-Based Guideline for the Management of Patients With Residual or Recurrent Nonfunctioning Pituitary Adenomas. , 2016, Neurosurgery.