Противоотечная терапия глюкокортикоидами у пациентов с глиомами: за и против
https://doi.org/10.17650/1683-3295-2023-25-2-106-113
Аннотация
Цель работы – повышение уровня осведомленности о существующих схемах противоотечной терапии дексаметазоном у врачей разных специальностей (нейрохирургов, неврологов, реаниматологов, эндокринологов). На основании данных научной литературы авторы дают подробное описание используемых ранее и существующих в настоящее время схем противоотечной терапии глюкокортикоидами (в частности, дексаметазоном) у пациентов с первичными и вторичными опухолями головного мозга и его оболочек. Авторы оценивают различные схемы назначения дексаметазона (от 2 до 64 мг / сут с дробным введением и однократные дозировки до 20 мг) пациентам с опухолями глиального ряда в плане эффективности терапии. Дан анализ рисков возникновения побочных эффектов и осложнений терапии. Выделены 3 группы рисков: ранние (нарушения углеводного обмена, психоэмоциональные симптомы, артериальная гипертензия, прибавка массы тела), поздние (экзогенный гиперкортицизм, нарушения липидного обмена, проксимальная миопатия, остеопороз, язвенная болезнь желудка и двенадцатиперстной кишки, иммуносупрессивные состояния) и возникающие на фоне резкой отмены препарата (надпочечниковая недостаточность). В заключение авторы отметили способы возможного предотвращения и уменьшения побочных эффектов.
Ключевые слова
Об авторах
А. В. ПриродовРоссия
129090 Москва, Большая Сухаревская пл., 3; 117997 Москва, ул. Островитянова, 1
П. И. Соловьева
Россия
129090 Москва, Большая Сухаревская пл., 3
И. А. Хрипун
Россия
344022 Ростов-на-Дону, пер. Нахичеванский, 29
М. М. Микаилов
Россия
129090 Москва, Большая Сухаревская пл., 3
Список литературы
1. Miller K.D., Ostrom Q.T., Kruchko C. et al. Brain and other central nervous system tumor statistics, 2021. CA Cancer J Clin 2021;71(5):381–406. DOI: 10.3322/caac.21693
2. Siegel R.L., Miller K.D., Fuchs H.E. et al. Cancer Statistics 2021. CA Cancer J Clin 2021;71(1):7–33. DOI: 10.3322/caac.21654
3. Ostrom Q.T., Patil N., Cioffi G. et al. CBTRUS statistical report: primary brain and other central nervous system tumors diagnosed in the United States in 2013–2017. Neuro Oncol 2020;22(12 Suppl 2):iv1–96. DOI: 10.1093/neuonc/noaa200
4. Ostrom Q.T., Cote D.J., Ascha M. et al. Adult glioma incidence and survival by race or ethnicity in the United States from 2000 to 2014. JAMA Oncol 2018;4(9):1254–62. DOI: 10.1001/jamaoncol.2018.1789
5. Ostrom Q.T., Rubin J.B., Lathia J.D. et al. Females have the survival advantage in glioblastoma. Neuro Oncol 2018;20(4):576–7. DOI: 10.1093/neuonc/noy002
6. Wen P.Y., Kesari S. Malignant gliomas in adults. N Engl J Med 2008;359(5):492–507. DOI: 10.1056/NEJMra0708126
7. Hedley-Whyte E.T., Hsu D.W. Effect of dexamethasone on bloodbrain barrier in the normal mouse. Ann Neurol 1986;19(4):373–7. DOI: 10.1002/ana.410190411
8. Roth P., Regli L., Tonder M. et al. Tumor-associated edema in brain cancer patients: pathogenesis and treatment. Expert Rev Anticancer Ther 2013;13(11):1319–25. DOI: 10.1586/14737140.2013.852473
9. Stummer W. Mechanisms of tumor-related brain edema. Neurosurg Focus 2007;22(5):E8. DOI: 10.3171/foc.2007.22.5.9
10. Lin K.T., Wang L.H. New dimension of glucocorticoids in cancer treatment. Steroids 2016;11:84–8. DOI: 10.1016/j.steroids.2016.02.01
11. Kaur C., Ling E.A. Blood brain barrier in hypoxic-ischemic conditions. Curr Neurovasc Res 2008;5(1):71–81. DOI: 10.2174/156720208783565645
12. Wolburg H., Lippoldt A. Tight junctions of the blood-brain barrier: development, composition and regulation. Vascul Pharmacol 2002;38(6):323–37. DOI: 10.1016/S1537-1891(02)00200-8
13. Zlokovic B.V. The blood-brain barrier in health and chronic neurodegenerative disorders. Neuron 2008;57(2):178–201. DOI: 10.1016/j.neuron.2008.01.003
14. Zozulya A., Weidenfeller C., Galla H.J. Pericyte-endothelial cell interaction increases MMP-9 secretion at the blood-brain barrier in vitro. Brain Res 2008;1189:1–11. DOI: 10.1016/j.brainres.2007.10.099
15. Kubota K., Furuse M., Sasaki H. et al. Ca2+-independent celladhesion activity of claudins, a family of integral membrane proteins localized at tight junctions. Curr Biol 1999;9(18):1035–8. DOI: 10.1016/s0960-9822(99)80452-7
16. Wolburg H., Noell S., Fallier-Becker P. et al. The disturbed bloodbrain barrier in human glioblastoma. Mol Aspects Med 2012;33(5– 6):579–89. DOI: 10.1016/j.mam.2012.02.003
17. Dubois L.G., Campanati L., Righy C. et al. Gliomas and the vascular fragility of the blood brain barrier. Front Cell Neurosci 2014;8:418. DOI: 10.3389/fncel.2014.00418
18. Salmaggi A., Gelati M., Pollo B. et al. CXCL12 in malignant glial tumors: a possible role in angiogenesis and cross-talk between endothelial and tumoral cells. J Neurooncol 2004;67(3):305–17. DOI: 10.1023/b:neon.0000024241.05346.24
19. Papadopoulos M.C., Saadoun S., Woodrow C.J. et al. Occludin expression in microvessels of neoplastic and non-neoplastic human brain. Neuropathol Appl Neurobiol 2001;27(5): 384–95. DOI: 10.1046/j.0305-1846.2001.00341.x
20. Raslan A., Bhardwaj A. Medical management of cerebral edema. Neurosurg Focus 2007;22(5):E12. DOI: 10.3171/foc.2007.22.5.13
21. Galicich J.H., French L.A., Melby J.C. Use of dexamethasone in treatment of cerebral edema associated with brain tumors. J Lancet 1961;81:46–53. PMID: 13703072
22. Salvador E., Shityakov S., Förster C. Glucocorticoids and endothelial cell barrier function. Cell Tissue Res 2014;355(3): 597–605. DOI: 10.1007/s00441-013-1762-z
23. Kotsarini S., Griffiths P.D., Wilkinson I.D. et al. A systematic review of the literature on the effects of dexamethasone on the brain from in vivo human studies: implications for physiological brain imaging in patients with intracranial tumors. Neurosurgery 2010;67(6):1799–815. DOI: 10.1227/NEU.0b013e3181fa775b
24. Kim H., Lee J.M., Park J.S. et al. Dexamethasone regulates angiopoietin-1 and VEGF in a coordinated manner: a mechanism for glucocorticoid-induced stabilization of the blood-brain barrier. Biochem Biophys Res Commun 2008;372(1):243–8. DOI: 10.1016/j.bbrc.2008.05.025
25. Lim-Fat M.J., Bi W.L., Lo J. et al. Letter: When Less is More: Dexamethasone Dosing for Brain Tumors. Neurosurgery 2019;85(3):E607–8. DOI: 10.1093/neuros/nyz186
26. Мокрышева Н.Г., Мельниченко Г.А., Адамян Л.В. и др. Клинические рекомендации «Врожденная дисфункция коры надпочечников (адреногенитальный синдром)». Ожирение и метаболизм 2021;18(3):345–82. DOI: 10.14341/omet12787
27. Marty R., Cain M.L. Effects of corticosteroid (dexamethasone) administration on the brain scan. Radiology 1973;107(1):117–21. DOI: 10.1148/107.1.117
28. Fletcher J.W., George E.A., Henry R.E. et al. Brainscans, dexamethasone therapy, and brain tumors. JAMA 1975;232(12):1261–3.
29. Graham K., Caird F.I. High-dose steroid therapy of intracranial tumour in the elderly. Age Ageing 1978;7(3):146–50. DOI: 10.1093/ageing/7.3.146
30. Pezner R.D., Lipsett J.A. Peptic ulcer disease and other complications in patients receiving dexamethasone palliation for brain metastasis. West J Med 1982;137(5):375–8. PMID: 6184892
31. Muller W., Kretzschmar K., Schicketanz K.H. CT-analyses of cerebral tumors under steroid therapy. Neuroradiology 1984;26(4):293–8. DOI: 10.1007/BF00339773
32. Vecht C.J., Hovestadt A., Verbiest H.B. et al. Dose-effect relationship of dexamethasone on Karnofsky performance in metastatic brain tumors: a randomized study of doses of 4, 8, and 16 mg per day. Neurology 1994;44(4):675–80. DOI: 10.1212/wnl.44.4.675
33. Dietrich J., Rao K., Pastorino S. et al. Corticosteroids in brain cancer patients: benefits and pitfalls. Expert Rev Clin Pharmacol 2011;4(2):233–42. DOI: 10.1586/ecp.11.1
34. Dubinski D., Won S.Y., Gessler F. et al. Dexamethasone-induced leukocytosis is associated with poor survival in newly diagnosed glioblastoma. J Neurooncol 2018;137(3):503–10. DOI: 10.1007/s11060-018-2761-4
35. Patel R., Bookout A.L., Magomedova L. et al. Glucocorticoids regulate the metabolic hormone FGF21 in a feed-forward loop. Mol Endocrinol 2015;29(2):213–3. DOI: 10.1210/me.2014-1259
36. Ryken T.C., McDermott M., Robinson P.D. et al. The role of steroids in the management of brain metastases: a systematic review and evidence-based clinical practice guideline. J Neurooncol 2010;96(1):103–14. DOI: 10.1007/s11060-009-0057-4
37. Kostaras X., Cusano F., Kline G.A. et al. Use of dexamethasone in patients with high-grade glioma: a clinical practice guideline. Curr Oncol 2014;21(3):e493–503. DOI: 10.3747/co.21.1769
38. Expert Panel on Radiation Oncology-Brain Metastases, Lo S.S., Gore E.M., Bradley J.D. et al. ACR Appropriateness Criteria® pre-irradiation evaluation and management of brain metastases. J Palliat Med 2014;17(8):880–6. DOI: 10.1089/jpm.2014.9417
39. Greenberg M.S. Handbook of Neurosurgery: 9th ed. Thieme Verlagsgruppe, 2019. 1784 p.
40. Sarin R., Murthy V. Medical decompressive therapy for primary and metastatic intracranial tumours. Lancet Neurol 2003;2(6):357–65. DOI: 10.1016/s1474-4422(03)00410-1
41. Jessurun C.A.C., Hulsbergen A.F.C., Lamba N. et al. Practice variation in perioperative steroid dosing for brain tumor patients: an international survey. World Neurosurg 2022; 159:e431–41. DOI: 10.1016/j.wneu.2021.12.067
42. Jessurun C.A.C., Hulsbergen A.F.C., Cho L.D. et al. Evidencebased dexamethasone dosing in malignant brain tumors: what do we really know? J Neurooncol 2019;144(2):249–64. DOI: 10.1007/s11060-019-03238-4
43. Fardet L., Cabane J., Lebbé C. et al. Incidence and risk factors for corticosteroid lipodystrophy: a prospective study. J Am Acad Dermatol 2007;57(4):604–9. DOI: 10.1016/j.jaad.2007.04.018
44. Dropcho E.J., Soong S.J. Steroid-induced weakness in patients with primary brain tumors. Neurology 1991;41(8):1235–9. DOI: 10.1212/wnl.41.8.1235
45. Galicich J.H., French L.A. Use of dexamethasone in the treatment of cerebral edema resulting from brain tumors and brain surgery. Am Pract Dig Treat 1961;12:169–74. PMID: 13703073
46. Gere S.P., Grossman S.A. Interstitial fluid flow along white matter pathways: a potentially important mechanism for the spread of primary brain tumors. J Neurooncol 1997;32(3):193–201. DOI: 10.1023/a:1005761031077
47. Sanderkok P.A., Soane T. Corticosteroids in acute ischemic stroke. Cochrane Database Syst Rev 2011;2011(9):CD00064. DOI: 10.1002/14651858.CD000064.pub2
48. Kaal E.C., Vecht C.J. Treatment of cerebral edema in brain tumors. Curr Opin Oncol 2004;16(6):593–600. DOI: 10.1097/01.cco.0000142076.52721.b3
49. Doumeizel P.M., Robin F., Ballerie A. et al. Side effects of longterm oral corticosteroid therapy. Rev Prat 2021;71(6):587–96. PMID: 34553543
50. Hempen C., Weiss E., Hess C.F. Dexamethasone treatment in patients with brain metastases and primary brain tumors: do the benefits outweigh the side-effects? Support Care Cancer 2002;10(4):322–8. DOI: 10.1007/s00520-001-0333-0
51. Dubinski D., Hattingen E., Senft C. et al. Controversial roles for dexamethasone in glioblastoma – Opportunities for novel vascular targeting therapies. J Cereb Blood Flow Metab 2019;39(8):1460–8. DOI: 10.1177/0271678X19859847
52. Beaupere C., Liboz A., Fève B. et al. Molecular mechanisms of glucocorticoid-induced insulin resistance. Int J Mol Sci 2021;22(2):623. DOI: 10.3390/ijms22020623
53. Moghadam-Kia S., Werth V.P. Prevention and treatment of systemic glucocorticoid side effects. Int J Dermatol 2010;49(3):239–48. DOI: 10.1111/j.1365-4632.2009.04322.x
54. Hodgens A., Sharman T. Corticosteroids. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing, 2022 Jan. 2021 Oct 16.
55. Ericson-Neilsen W., Kaye A.D. Steroids: pharmacology, complications, and practice delivery issues. Ochsner J 2014;14(2):203–7.
56. Noetzlin S., Breville G., Seebach J.D. et al. Short-term glucocorticoid-related side effects and adverse reactions: a narrative review and practical approach. Swiss Med Wkly 2022;152:w30088. DOI: 10.4414/smw.2022.w30088
57. Liu D., Ahmet A., Ward L. et al. A practical guide to the monitoring and management of the complications of systemic corticosteroid therapy. Allergy Asthma Clin Immunol 2013;9(1):30. DOI: 10.1186/1710-1492-9-30
58. Cenciarini M., Valentino M., Belia S. et al. Dexamethasone in Glioblastoma Multiforme Therapy: Mechanisms and Controversies. Front Mol Neurosci 2019;12:65. DOI: 10.3389/fnmol.2019.00065
59. Kostaras X., Shea-Budgell M.A., Malcolm E. et al. Is there a role for clinical practice guidelines in multidisciplinary tumor board meetings? A descriptive study of knowledge transfer between research and practice. J Cancer Educ 2012;27(1):42–5. DOI: 10.1007/s13187-011-0263-6
60. Shields L.B.E., Shelton B.J., Shearer A.J. et al. Dexamethasone administration during definitive radiation and temozolomide renders a poor prognosis in a retrospective analysis of newly diagnosed glioblastoma patients. Radiat Oncol 2015;10:222. DOI: 10.1186/s13014-015-0527-0
61. Zhou L., Shen Y., Huang T. et al. The prognostic effect of dexamethasone on patients with glioblastoma: a systematic review and meta-analysis. Front Pharmacol 2021;12:727707. DOI: 10.3389/fphar.2021.727707
62. Wong E.T., Lok E., Gautam S. et al. dexamethasone exerts profound immunologic interference on treatment efficacy for recurrent glioblastoma. Br J Cancer 2015;113(2):232–41. DOI: 10.1038/bjc.2015.238
63. Lee C., Ahn S., Park J.S. et al. Effect of cumulative dexamethasone dose during concomitant chemoradiation on lymphopenia in patients with newly diagnosed glioblastoma. Brain Tumor Res Treat 2020;8(2):71–6. DOI: 10.14791/btrt.2020.8.e12
64. Iorgulescu J.B., Gokhale P.C., Speranza M.C. et al. Concurrent dexamethasone limits the clinical benefit of immune checkpoint blockade in glioblastoma. Clin Cancer Res 2021;27(1):276–87. DOI: 10.1158/1078-0432.CCR-20-2291
65. Gu Y.T., Xue Y.X., Wang P. et al. Dexamethasone enhances calcium-activated potassium channel expression in bloodbrain tumor barrier in a rat brain tumor model. Brain Res 2009;1259:1–6. DOI:10.1016/j.brainres.2008.12.080
66. Hempen C., Elfering S., Mulder A.H. et al. Dexamethasone suppression test: development of a method for simultaneous determination of cortisol and dexamethasone in human plasma by liquid chromatography/tandem mass spectrometry. Ann Clin Biochem 2012;49(Pt2):170–6. DOI: 10.1258/acb.2011.011004
67. Derr R.L., Ye X., Islas M.U. et al. Association between hyperglycemia and survival in patients with newly diagnosed glioblastoma. J Clin Oncol 2009;27(7):1082–6. DOI: 10.1200/JCO.2008.19.1098
68. Arvold N.D., Armstrong T.S., Warren K.E. et al. Corticosteroid use endpoints in neuro-oncology: Response Assessment in NeuroOncology Working Group. Neuro Oncol 2018;20(7):897–906. DOI: 10.1093/neuonc/noy056
69. Ali Z., Shah M.A., Mir S.A. et al. Effects of single dose of dexamethasone on perioperative blood glucose levels in patients undergoing surgery for supratentorial tumors – An Observational Study. Anest Essays Res 2020;14(1):56–61. DOI: 10.4103/aer.AER_21_20
70. Derr R.L., Ye X., Islas M.U. et al. Association between hyperglycemia and survival in patients with newly diagnosed glioblastoma. J Clin Oncol 2009;27(7):1082–6. DOI: 10.1200/JCO.2008.19.1098
71. Hagan K., Bhavsar S., Arunkumar R. et al. Association between perioperative hyperglycemia and survival in patients with glioblastoma. J Neurosurg Anesthesiol 2017;29(1):21–9. DOI: 10.1097/ANA.0000000000000339
72. Keshwani K., Raymond L., Shawe-Taylor M. et al. Effect of early integration of diabetic services in primary brain tumor patients receiving radical radiotherapy on steroid-induced diabetic complications and hospital admission. J Clin Oncol 2020; 38(15 Suppl) 2020 ASCO Annual Meeting I. DOI: 10.1200/JCO.2020.38.15_suppl.e14522 Доступно по: https://ascopubs.org/doi/abs/10.1200/JCO.2020.38.15_suppl.e14522.
73. Pantelidis P., Tsitsopoulos P.P., Pappa E. et al. The effect of diabetes mellitus on in-hospital hyperglycemia, length of stay and survival in patients with brain tumor receiving dexamethasone: A descriptive and comparative analysis. Clin Neurol Neurosurg 2019;184:105450. DOI: 10.1016/j.clineuro.2019.105450
74. Barbero-Bordallo N., Gomez-Vicente L. Use of steroids in neurooncology. Rev Neurol 2019;68(9):389–97. DOI: 10.33588/rn.6809.2019083
75. Afshari A.R., Sanati M., Aminyavari S. et al. Advantages and drawbacks of dexamethasone in glioblastoma multiforme. Crit Rev Oncol Hematol 2022;172:103625. DOI: 10.1016/j.critrevonc.2022.103625
76. Olson J.J., Ryken T. Guidelines for the treatment of newly diagnosed glioblastoma: introduction. J Neurooncol 2008;89(3):255–8. DOI: 10.1007/s11060-008-9595-4
77. Restrictive Use of Dexamethasone in Glioblastoma (RESDEX). University Hospital Inselspital, Berne. 2020-. ClinicalTrials.gov Identifier: NCT04266977. Доступно по: https://cr.minzdrav.gov.ru/schema/578_1
78. Первичные опухоли центральной нервной системы: клинические рекомендации. М., 2020. Доступно по: https://www.ruans.org/Text/Guidelines/primary-tumors-of-cns-2020.pdf
79. Об утверждении стандартов медицинской помощи взрослым при первичных опухолях центральной нервной системы. Приказ Минздрава России от 13 апреля 2021 г. № 346н. Доступно по: https://docs.cntd.ru/document/603591177
Рецензия
Для цитирования:
Природов А.В., Соловьева П.И., Хрипун И.А., Микаилов М.М. Противоотечная терапия глюкокортикоидами у пациентов с глиомами: за и против. Нейрохирургия. 2023;25(2):106-113. https://doi.org/10.17650/1683-3295-2023-25-2-106-113
For citation:
Prirodov A., Solovyeva P.I., Khripun I.A., Mikailov M.M. The use of glucocorticoids in the treatment of cerebral edema for glioma tumour patients: Pro and Contra. Russian journal of neurosurgery. 2023;25(2):106-113. (In Russ.) https://doi.org/10.17650/1683-3295-2023-25-2-106-113