Preview

Russian journal of neurosurgery

Advanced search

Metabolic navigation during brain tumor surgery: analysis of a series of 403 patients

https://doi.org/10.17650/1683-3295-2022-24-4-46-58

Abstract

Introduction. Metabolic navigation with 5‑ALA is one of methods for intraoperative imaging in neuro‑oncology.

Aim. To perform a comparative analysis of sensitivity of metabolic navigation with 5‑ALA during surgery of primary and secondary brain tumors of various histological nature and degree of malignancy.

Materials and methods. During the period from 2013 to 2020, our group have performed surgery to 403 patients using metabolic navigation: microsurgical resections were performed in 384 people with brain tumors, 220 of them were with glial tumors, 101 were with intracranial meningiomas, 63 were with metastatic brain damage. Among patients with metastases, 39 patients had a solitary injury, 16 had a multi‑focal injury, so 72 cases of metastatic nodes were considered in this group. Stereotactic biopsies with 5‑ALA‑assistance were performed in 19 people. Metabolic navigation was performed with the drug 5‑ALA, which was taken orally at a dose of 20 mg/kg 2 hours before surgery. Intraoperative fluorescence was evaluated using microscope with a fluorescent module.

Results. Metabolic navigation using microscope has a high sensitivity when employed during microsurgery (including repeated implementation of surgery) in cases of anaplastic gliomas (65 % in total, 58 % with bright glow), glioblastomas (94 % in total, 53 % with bright glow), intracranial meningiomas (94 % in total, 64 % – with bright glow). The use of 5‑ALA has significant limitations in sensitivity in cases of diffuse gliomas (46 % – in total, 27 % – with bright glow) and brain metastases (in total 87 % – for the solid part, 52 % – for the bed, with bright glow – 51 %). In diffuse gliomas, the glow areas had significantly higher proliferative index and cell nuclei density than the fluoronegative zones. Among the most important factors affecting the glow of gliomas it can be noted: the status of the IDH1 mutation, the volume of the contrasting part of the glioma according to MRI data, the methionine accumulation index according to positron emission tomography, the tumor blood flow indicators according to the arterial spin marking method – ASL perfusion.

Conclusions. Implementation of 5‑ALA navigation with the use of microscope provides high sensitivity in cases of glioblastomas, anaplastic gliomas (especially for detecting of non‑contrasting part of tumor that is not visually altered in the white light of operating microscope) and brain meningiomas. The method is less effective in low‑grade gliomas and intracranial metastases.

About the Authors

S. A. Goryaynov
N. N. Burdenko National Medical Research Center of Neurosurgery, Ministry of Health of Russia; Immanuel Kant Baltic Federal University
Russian Federation

Sergey Alekseevich Goryaynov

16 4th Tverskaya-Yamskaya St., Moscow 125047

14 Al. Nevskogo St., Kaliningrad 236041



A. A. Potapov
N. N. Burdenko National Medical Research Center of Neurosurgery, Ministry of Health of Russia
Russian Federation

16 4th Tverskaya-Yamskaya St., Moscow 125047



V. A. Okhlopkov
N. N. Burdenko National Medical Research Center of Neurosurgery, Ministry of Health of Russia
Russian Federation

16 4th Tverskaya-Yamskaya St., Moscow 125047



A. I. Batalov
N. N. Burdenko National Medical Research Center of Neurosurgery, Ministry of Health of Russia
Russian Federation

16 4th Tverskaya-Yamskaya St., Moscow 125047



R. O. Afandiev
N. N. Burdenko National Medical Research Center of Neurosurgery, Ministry of Health of Russia
Russian Federation

16 4th Tverskaya-Yamskaya St., Moscow 125047



A. Yu. Belyaev
N. N. Burdenko National Medical Research Center of Neurosurgery, Ministry of Health of Russia
Russian Federation

16 4th Tverskaya-Yamskaya St., Moscow 125047



A. A. Aristov
N. N. Burdenko National Medical Research Center of Neurosurgery, Ministry of Health of Russia
Russian Federation

16 4th Tverskaya-Yamskaya St., Moscow 125047



T. A. Caveleva
Prokhorov General Physics Institute, Russian Academy of Sciences
Russian Federation

38 Vavilova St., Moscow 119991



V. Yu. Zhukov
N. N. Burdenko National Medical Research Center of Neurosurgery, Ministry of Health of Russia
Russian Federation

16 4th Tverskaya-Yamskaya St., Moscow 125047



V. B. Loshchenov
Prokhorov General Physics Institute, Russian Academy of Sciences
Russian Federation

38 Vavilova St., Moscow 119991



D. V. Gusev
The Russian National Research Medical University named after N. I. Pirogov
Russian Federation

1 Ostrovitianov St., Moscow 117997



N. E. Zakharova
N. N. Burdenko National Medical Research Center of Neurosurgery, Ministry of Health of Russia
Russian Federation

16 4th Tverskaya-Yamskaya St., Moscow 125047



References

1. Potapov A.A., Goryaynov S.A., Okhlopkov V.A. et al. Clinical guidelines for the use of intraoperative fluorescence diagnosis in brain tumor surgery. Zhurnal voprosy neirokhirurgii im. N.N. Burdenko = Burdenko’s Journal of Neurosurgery 2015;79(5):91–101. (In Russ.). DOI: 10.17116/neiro201579591-101

2. Stummer W., Pichlmeier U., Meinel T. et al. Fluorescence-guided surgery with 5-aminolevulinic acid for resection of malignant glioma: a randomised controlled multicentre phase III trial. Lancet Oncol 2006;7(5):392–401. DOI: 10.1016/S1470-2045(06)70665-9

3. Valdes P.A., Kim A., Leblond F. et al. Combined fluorescence and reflectance spectroscopy for in vivo quantification of cancer biomarkers in low- and high-grade glioma surgery. J Biomed Opt 2011;16(11):116007. DOI: 10.1117/1.3646916

4. Moore G.E. Fluorescein as an agent in the differentiation of normal and malignant tissues. Science 1947;106(2745):130–1. DOI: 10.1126/science.106.2745.130-a

5. Stummer W., Novotny A., Stepp H. et al. Fluorescence-guided resection of glioblastoma multi-forme by using 5-aminolevulinic acid-induced porphyrins: a prospective study in 52 consecutive patients. J Neurosurg 2000;93(6):1003–13. DOI: 10.3171/jns.2000.93.6.1003

6. Coluccia D., Fandino J., Fujioka M. et al. Intraoperative 5-aminolevulinic-acid-induced fluorescence in meningiomas. Acta Neurochir (Wien) 2010;152(10):1711–9. DOI: 10.1007/s00701-010-0708-4

7. Kamp M.A., Fischer I., Buhner J. et al. 5-ALA fluorescence of cerebral metastases and its impact for the local-in-brain progression. Oncotarget 2016;7(41):66776–89. DOI: 10.18632/oncotarget.11488

8. Kamp M.A., Munoz-Bendix C., Mijderwijk H.J. et al. Is 5-ALA fluorescence of cerebral metastases a prognostic factor for local recurrence and overall survival? J Neurooncol 2019;141(3):547–53. DOI: 10.1007/s11060-018-03066-y

9. Eicker S.O., Floeth F.W., Kamp M. et al. The impact of fluorescence guidance on spinal intradural tumour surgery. Eur Spine J 2013;22(6):1394–401. DOI: 10.1007/s00586-013-2657-0

10. Widhalm G., Kiesel B., Woehrer A. et al. 5-Aminolevulinic acid induced fluorescence is a powerful intraoperative marker for precise histopathological grading of gliomas with non-significant contrast-enhancement. PLoS ONE 2013;8(10):e76988. DOI: 10.1371/journal.pone.0076988

11. Goryaynov S.A., Widhalm G., Goldberg M.F. et al. The role of 5-ALA in low-grade gliomas and the influence of antiepileptic drugs on intraoperative fluorescence. Front Oncol 2019;9:423. DOI: 10.3389/fonc.2019.00423

12. Goryaynov S.A., Okhlopkov V.A., Golbin D.A. et al. Fluorescence diagnosis in neurooncology: retrospective analysis of 653 cases. Front Oncol 2019;9:830. DOI: 10.3389/fonc.2019.00830

13. Potapov A.A., Goryaynov S.A., Okhlopkov V.A. et al. Laser biospectroscopy and 5-ALA fluorescence navigation as a helpful tool in the meningioma resection. Neurosurg Rev 2016;39(3):437–47. DOI: 10.1007/s10143-015-0697-0

14. Millesi M., Kiesel B., Mischkulnig M. et al. Analysis of the surgical benefits of 5-ALA-induced fluorescence in intracranial meningiomas: experience in 204 meningiomas. J Neurosurg 2016;125(6):1408–19. DOI: 10.3171/2015.12.JNS151513

15. Kurzhupov M.I. Intraoperative fluorescence diagnostics and photo-dynamic therapy in patients with metastatic brain damage. Diss. … candidate of medical sciences. Moscow, 2011. (In Russ.).

16. Catapano G., Sgulo F.G., Seneca V. et al. Fluorescein-assisted stereotactic needle biopsy of brain tumors: a single-center experience and systematic review. Neurosurg Rev 2019;42(2): 309–18. DOI: 10.1007/s10143-018-0947-z

17. Widhalm G., Minchev G., Woehrer A. et al. Strong 5-aminolevulinic acid-induced fluorescence is a novel intraoperative marker for representative tissue samples in stereotactic brain tumor biopsies. Neurosurg Rev 2012;35(3):381–91. DOI: 10.1007/s10143-012-0374-5

18. Corns R., Mukherjee S., Johansen A., Sivakumar G. 5-aminolevulinic acid guidance during awake craniotomy to maximise extent of safe resection of glioblastoma multiforme. BMJ Case Rep 2015;2015:bcr2014208575. DOI: 10.1136/bcr-2014-208575

19. Valdes P.A., Millesi M., Widhalm G., Roberts D.W. 5-aminolevulinic acid induced protoporphyrin IX (ALA-PpIX) fluorescence guidance in meningioma surgery. J Neurooncol 2019;141(3):555–65. DOI: 10.1007/s11060-018-03079-7


Review

For citations:


Goryaynov S.A., Potapov A.A., Okhlopkov V.A., Batalov A.I., Afandiev R.O., Belyaev A.Yu., Aristov A.A., Caveleva T.A., Zhukov V.Yu., Loshchenov V.B., Gusev D.V., Zakharova N.E. Metabolic navigation during brain tumor surgery: analysis of a series of 403 patients. Russian journal of neurosurgery. 2022;24(4):46-58. https://doi.org/10.17650/1683-3295-2022-24-4-46-58

Views: 543


Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 License.


ISSN 1683-3295 (Print)
ISSN 2587-7569 (Online)
X