Magnetotherapy in Experimental and Clinical Neuro-Oncology: A Review
DOI:
https://doi.org/10.30683/1927-7229.2023.12.08Keywords:
Neuro-oncology, malignant brain tumors, treatment, magnetotherapyAbstract
The purpose of this publication is not to state the fact of the high antitumor effectiveness of the gold standard treatment of malignant brain tumors (surgical intervention with adjuvant chemoradiotherapy), but to consider the possibility of using alternative therapeutic options, in particular, magnetotherapy, as a component of the treatment of patients with this serious pathology, as well as a method of preventing a number of postoperative adverse reactions.
References
Khan S, El Kouatly M, Kambris ET, et al. Epidemiology of brain tumors in the United Arab Emirates: a national registry cross sectional study. BMC Neurology 2020; 20: 301. https://doi.org/10.1186/s12883-020-01869-z
GBD 2016 Brain and Other CNS Cancer Collaborators. Global, regional, and national burden of brain and other CNS cancer, 1990 – 2016: a systematic analysis for the global burden of disease study 2016. Lancet Neurol 2019; 18: 376-93. https://doi.org/10.1016/S1474-4422(18)30468-X
Chang SM, Parney IF, Huang W, et al. Patterns of care for adults with newly diagnosed malignant glioma. JAMA 2005; 293: 557-64. https://doi.org/10.1001/jama.293.5.557
Pouchieu С, Gruber A, Berteaud E, et al. Increasing incidence of central nervous system (CNS) tumors (2000-2012): findings from a population based registry in Gironde (France). BMC Cancer 2018; 18(1): 1-13. https://doi.org/10.1186/s12885-018-4545-9
Omuro A, DeAngelis LM. Glioblastoma and other malignant gliomas. A clinical review. JAMA 2013; 310(17): 1842-50. https://doi.org/10.1001/jama.2013.280319
Nieder C, Grosu AL, Molls M. A comparison of treatment results for recurrent malignant gliomas. Cancer Treat Rev 2000; 26: 397-409. https://doi.org/10.1053/ctrv.2000.0191
Lacroix M, Abi-Said D, Fourney DR, et al. A multivariate analysis of 416 patients with glioblastoma multiforme: prognosis, extent of resection, and survival. J Neurosurg 2001; 95(2): 190-98. https://doi.org/10.3171/jns.2001.95.2.0190
Tserkovsky DA. Photodynamic therapy of malignant brain tumors: the current state of the problem. Oncol J 2011; 5(1): 129-38 (in Russian).
Roth P, Gramatzki D, Weller M. Management of elderly patients with glioblastoma. Curr Neurol Neurosci Rep 2017; 17(4): 1-22. https://doi.org/10.1007/s11910-017-0740-3
Yousuf A, Oliva CR, Noman ASM, et al. Radioresistance in glioblastoma and the development of radiosensitizers. Cancers (Basel) 2020; 12(9): 2511. https://doi.org/10.3390/cancers12092511
Pletnev AS, Ulashchik VS. Magnetic fields in experimental and clinical oncology. Minsk: Belorusskaya navuka, 2016; p. 229 (in Russian).
Magnetotherapy: theoretical foundations and practical application. under the general editorship of Prof. V.S. Ulashchik. Minsk. 2015; p. 379 (in Russian).
Akbarnejad Z, Eskandary H, Vergallo C, et al. Effects of extremely low-frequency pulsed electromagnetic field on glioblastoma cells (U87). Electromagn Biol Med 2017; 36(3): 238-47. https://doi.org/10.1080/15368378.2016.1251452
Akbarnejad Z, Eskandary H, Dini L, et al. Cytotoxicity of temozolomide on human glioblastoma cells is enhanced by the concomitant exposure to an extremely low-frequency electromagnetic field (100Hz, 100G). Biomed Pharmacother 2017; 92: 254-64. https://doi.org/10.1016/j.biopha.2017.05.050
Atmachidi DP. Adjuvant chemoradiotherapy with the use of a magnetic field in the complex treatment of malignant glial brain tumors: abstract. dis. Candidate of Medical Sciences. Rostov on Don, 2009; p. 27 (in Russian).
Popov IA, Shixliarova AI, Rostorguev EE, et al. Inhibitory effect of pulsed magnetic fields and ionizing radiation on human glioblastoma cell culture T98G. Med Bull North Caucasus 2019; 14(1.2): 228-31 (in Russian). https://doi.org/10.14300/mnnc.2019.14021
Sidorenko YuS, Kit OI, Popov IA, et al. The influence of pulsed magnetic fields on the expression of oncosuppressor genes in an experiment on human glioblastoma cell culture T98G. Siber Oncol J 2019; 18(6): 57-66 (in Russian). https://doi.org/10.21294/1814-4861-2019-18-6-57-66
Popov IA, Sidorenko YuS, Kit OI, et al. The use of pulsed transcranial magnetic stimulation (TMS) at the stages of complex treatment of patients with malignant gliomas of the brain. Neuroscience for medicine and psychology: XVI International Interdisciplinary Congress. Sudak, Crimea, Russia; October 6–16, 2020 Proceedings of the Congress. Edited by Loseva EV, Kryuchkova AV, Loginova NA. Moscow: MAKS Press. 2020; p. 380 (in Russian). https://doi.org/10.29003/m1213.sudak.ns2020-16/380-381
Popov IA. The use of transcranial electromagnetotherapy in the complex treatment of patients with malignant glial tumors of the brain: abstract. dis. Candidate of Medical Sciences. Rostov on Don, 2021; p. 26 (in Russian).
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