Ингибиторы тирозинкиназы Брутона в лечении рецидивов мантийноклеточной лимфомы с поражением ЦНС (два клинических наблюдения и обзор литературы)
ISSN (print) 1997-6933     ISSN (online) 2500-2139
2025-2
PDF_2025-18-2-184-196

Ключевые слова

мантийноклеточная лимфома
рецидивы с вовлечением ЦНС
ингибиторы тирозинкиназы Брутона
гематоэнцефалический барьер

Как цитировать

Куневич Е.О., Немсцверидзе Н.Н., Михалева М.А., Кувшинов А.Ю., Овчинникова Т.В., Корякина Е.В., Самарина С.В., Крутикова К.Ю., Сидоркевич С.В., Волошин С.В. Ингибиторы тирозинкиназы Брутона в лечении рецидивов мантийноклеточной лимфомы с поражением ЦНС (два клинических наблюдения и обзор литературы). Клиническая онкогематология. 2025;(2):184–196. doi:10.21320/2500-2139-2025-18-2-184-196.

Статистика

Просмотров аннотации: 5
PDF_2025-18-2-184-196 загрузок: 5

Ключевые слова

Аннотация

Мантийноклеточная лимфома (МКЛ) составляет 3–10 % всех вариантов неходжкинских лимфом и характеризуется агрессивным течением с частыми рецидивами и наличием экстранодальных поражений. В связи с появлением более эффективной системной противоопухолевой терапии и, как следствие, повышением продолжительности жизни пациентов частота рецидивов МКЛ с поражением ЦНС, по данным литературы, увеличилась до 4–20 %. Несмотря на широкое внедрение в клиническую практику таргетных препаратов, прогноз у пациентов с поражением ЦНС остается крайне неудовлетворительным. В качестве основной идеи в настоящей публикации выступает целесообразность применения при рецидивах МКЛ с поражением ЦНС препаратов из группы ингибиторов тирозинкиназы Брутона (BTK). Наиболее часто рекомендуется ибрутиниб как лекарственное средство, преодолевающее гематоэнцефалический барьер и обладающее высокой противоопухолевой активностью. Собственный опыт применения ибрутиниба при нейрорецидивах МКЛ представлен двумя клиническими наблюдениями. Одновременно широкому анализу подвергнуты соответствующие данные из литературы. Кроме того, в настоящем исследовании использовались данные 67 пациентов с МКЛ, которые получали лечение в гематологических стационарах различных медицинских учреждений Санкт-Петербурга и Ленинградской области с 2006 по 2023 г. Отчеты по двум клиническим наблюдениям составлены с учетом международных рекомендаций 2017 г. (CARE guidelines for case reports).

PDF_2025-18-2-184-196

Библиографические ссылки

  1. 1. Alaggio R, Amador C, Anagnostopoulos I. The 5th edition of the World Health Organization Classification of Haematolymphoid Tumours: Lymphoid Neoplasms. Leukemia. 2022;36(7):1720–48. doi: 10.1038/s41375-022-01620-2.
  2. 2. Pérez-Galán P, Dreyling M, Wiestne A. Mantle cell lymphoma: biology, pathogenesis, and the molecular basis of treatment in the genomic era. Blood. 2011;117(1):26–38. doi: 10.1182/blood-2010-04-189977.
  3. 3. Bertoni F, Rinaldi A, Zucca E, et al. Update on the molecular biology of mantle cell lymphoma. Hematol Oncol. 2006;4(1):22–7. doi: 10.1002/hon.767.
  4. 4. Zucca E, Roggero E, Pinotti G, et al. Patterns of survival in mantle cell lymphoma. Ann Oncol. 1995;6(3):257–62. doi: 10.1093/oxfordjournals.annonc.a059155.
  5. 5. Ghielmini M, Zucca E. How I treat mantle cell lymphoma. Blood. 2009;114(8):1469–76. doi: 10.1182/blood-2009-02-179739.
  6. 6. Montserrat E, Bosch F, López-Guillermo A, et al. CNS involvement in mantle-cell lymphoma. J Clin Oncol. 1996;14(3):941–4. doi: 10.1200/JCO.1996.14.3.941.
  7. 7. Cheah CY, George A, Giné E, et al. Central nervous system involvement in mantle cell lymphoma: clinical features, prognostic factors and outcomes from the European Mantle Cell Lymphoma Network. Ann Oncol. 2013;24(8):2119–23. doi: 10.1093/annonc/mdt139.
  8. 8. Wang ML, Rule S, Martin P, et al. Targeting BTK with ibrutinib in relapsed or refractory mantle-cell lymphoma. N Engl J Med. 2013;369(6):507–16. doi: 10.1056/NEJMoa1306220.
  9. 9. Lewis KL, Chin CK, Manos K, et al. Ibrutinib for central nervous system lymphoma: the Australasian Lymphoma Alliance/MD Anderson Cancer Center experience. Br J Haematol. 2021;192(6):1049–53. doi: 10.1111/bjh.16946.
  10. 10. Клеина Е.В. Генетическая стратификация и особенности клинического течения мантийноклеточной лимфомы: Дис. … канд. мед. наук. СПб., 2023. 174 с. [Kleina E.V. Geneticheskaya stratifikatsiya i osobennosti klinicheskogo techeniya mantiinokletochnoi limfomy. (Genetic stratification and clinical features of mantle cell lymphoma.) [dissertation] Saint Petersburg; 2023. 174 p. (In Russ)]
  11. 11. Riley DS, Barber MS, Kienle GS, et al. CARE guidelines for case reports: explanation and elaboration document. J Clin Epidemiol. 2017;89:218–35. doi: 10.1016/j.jclinepi.2017.04.026.
  12. 12. Bedotto J, Spier CM, Paquin ML, et al. Mantle zone lymphoma with central nervous system involvement. Cancer. 1986;58(9):2125–9. doi: 10.1002/1097-0142(19861101)58:9<2125::aid-cncr2820580927>3.0.co;2-t.
  13. 13. Ellison DJ, Turner RR, Van AR, et al. High-grade mantle zone lymphoma. Cancer. 1987;60(7):2717–20. doi: 10.1002/1097-0142(19820401)49:7<1429::aid-cncr2820490720>3.0.co;2-5.
  14. 14. Segal GH, Masih AS, Fox AC, et al. CD5-expressing B-cell non-Hodgkin’s lymphomas with bcl-1 gene rearrangement have a relatively homogeneous immunophenotype and are associated with an overall poor prognosis. Blood. 1995;85(6):1570–9. doi: 10.1182/blood.V85.6.1570.bloodjournal8561570.
  15. 15. Gagneten D, Hijazi YM, Jaffe ES, et al. Mantle cell lymphoma: a cytopathological and immunocytochemical study. Diagnostic Cytopathol. 1996;14(1):32–7. doi: 10.1002/(SICI)1097-0339(199602)14:1<32::AID-DC7>3.0.CO;2-X.
  16. 16. Kaleem Z, Wakoff AR, Smith RP, Hess JL. Blastic transformation of mantle cell lymphoma. Arch Pathol Lab Med. 1996;120(6):577–80.
  17. 17. Finsterer J, Lubec D, Jellinger K, et al. Recovery from coma caused by primary CNS mantle cell lymphoma presenting as encephalitis. Neurology. 1996;46(3):824–6. doi: 10.1212/wnl.46.3.824.
  18. 18. Bosch F, López-Guillermo A, Campo E, et al. Mantle cell lymphoma: presenting features, response to therapy, and prognostic factors. Cancer. 1998;82(3):567–75. doi: 10.1002/(sici)1097-0142(19980201)82:3<567::aid-cncr20>3.0.co;2-z.
  19. 19. Oinonen R, Franssila K, Elonen E. Central nervous system involvement in patients with mantle cell lymphoma. Ann Hematol. 1999;78(3):145–9. doi: 10.1007/s002770050491.
  20. 20. Valdez R, Kroft SH, Ross CW, et al. Cerebrospinal fluid involvement in mantle cell lymphoma. Mod Pathol. 2002;15(10):1073–9. doi: 10.1097/01.MP.0000030088.28684.5B.
  21. 21. Trip SA, Wroe SJ, Davies G, et al. Primary CNS mantle cell lymphoma associated with an isolated CSF monoclonal IgG band. Eur Neurol. 2003;49(3):187–8. doi: 10.1159/000069080.
  22. 22. Ladetto M, Sametti S, Astolfi M, et al. Central nervous system relapse in a patient with mantle cell lymphoma in continuous clinical and molecular remission at six years since autografting. Leuk Lymphoma. 2001;40(5–6):679–82. doi: 10.3109/10428190109097668.
  23. 23. Pachmann S, Bruning R, Schaffer M, et al. Suboccipital lateral injection of intrathecal chemotherapy in a patient with mantle cell lymphoma. Onkologie. 2004;27(1):68–71. doi: 10.1159/000075609.
  24. 24. Ferrer A, Bosch F, Villamor N, et al. Central nervous system involvement in mantle cell lymphoma. Ann Oncol. 2008;19(1):135–41. doi: 10.1093/annonc/mdm447.
  25. 25. Dierickx D, Wlodarska I, Vanhentenrijk V, et al. Secondary central nervous system involvement in cyclin D1-negative mantle cell lymphoma. Leuk Lymphoma. 2008;49(12):2365–6. doi: 10.1080/10428190802464737.
  26. 26. Wlodarska I, Dierickx D, Vanhentenrijk V, et al. Translocations targeting CCND2, CCND3, and MYCN do occur in t(11;14)-negative mantle cell lymphomas. Blood. 2008;111(12):5683–90. doi: 10.1182/blood-2007-10-118794.
  27. 27. Gill S, Herbert KE, Prince HM, et al. Mantle cell lymphoma with central nervous system involvement: frequency and clinical features. Br J Haematol. 2009;14(1):83–8. doi: 10.1111/j.1365-2141.2009.07835.x.
  28. 28. Gurevitz SA, Goldfarb JM, Cooper B, et al. Biopsy-proven mantle cell lymphoma in brain parenchyma. Proc (Bayl Univ Med Cent). 2011;24(1):45–7. doi: 10.1080/08998280.2011.11928681.
  29. 29. Doolittle ND, Abrey LE, Shenkier TN, et al. Brain parenchyma involvement as isolated central nervous system relapse of systemic non-Hodgkin lymphoma: an International Primary CNS Lymphoma Collaborative Group report. Blood. 2008;111(3):1085–93. doi: 10.1182/blood-2007-07-101402.
  30. 30. Conconi A, Franceschetti S, Lobetti-Bodoni C, et al. Risk factors of central nervous system relapse in mantle cell lymphoma. Lymphoma. 2013;54(9):1908–14. doi: 10.3109/10428194.2013.767454.
  31. 31. Chihara D, Asano N, Ohmachi K, et al. Ki-67 is a strong predictor of central nervous system relapse in patients with mantle cell lymphoma (MCL). Ann Oncol. 2015;26(5):966–73. doi: 10.1093/annonc/mdv074.
  32. 32. Wang ML, Blum KA, Martin P, et al. Long-term follow-up of MCL patients treated with single-agent ibrutinib: updated safety and efficacy results. Blood. 2015;126(6):739–45. doi: 10.1182/blood-2015-03-635326.
  33. 33. Dreyling M, Jurczak W, Jerkeman M, et al. Ibrutinib versus temsirolimus in patients with relapsed or refractory mantle-cell lymphoma: an international, randomised, open-label, phase 3 study. Lancet. 2016;387(10020):770–8. doi: 10.1016/S0140-6736(15)00667-4.
  34. 34. Rule S, Jurczak W, Jerkeman M, et al. Ibrutinib versus temsirolimus: 3-year follow-up of patients with previously treated mantle cell lymphoma from the phase 3, international, randomized, open-label RAY study. Leukemia. 2018;32(8):1799–803. doi: 10.1038/s41375-018-0023-2.
  35. 35. Bernard S, Goldwirt L, Amorim S, et al. Activity of ibrutinib in mantle cell lymphoma patients with central nervous system relapse. Blood. 2015;126(14):1695–8. doi: 10.1182/blood-2015-05-647834.
  36. 36. Dunleavy K, Lai CE, Roschewski M, et al. Phase I Study of Dose-Adjusted-Teddi-R with ibrutinib in untreated and relapsed/refractory primary CNS lymphoma. Blood. 2015;126(23):472. doi: 10.1182/blood.V126.23.472.472.
  37. 37. FDA. Clinical Pharmacology Reviews Ibrutinib 205552Orig1s000. Available from: https://www.accessdata.fda.gov/drugsatfda_docs/nda/2013/205552orig1s000clinpharmr.pdf (accessed 30.09.2024).
  38. 38. Mason C, Savona S, Rini JN, et al. Ibrutinib penetrates the blood brain barrier and shows efficacy in the therapy of Bing Neel syndrome [letter]. Br J Haematol. 2016;179(2):339–41. doi: 10.1111/bjh.14218.
  39. 39. Tucker DL, Naylor G, Kruger A, et al. Ibrutinib is a safe and effective therapy for systemic mantle cell lymphoma with central nervous system involvement – a multi-centre case series from the United Kingdom. Br J Haematol. 2017;178(2):327–9. doi: 10.1111/bjh.14122.
  40. 40. Mannina D, Loteta B. Ibrutinib treatment of mantle cell lymphoma relapsing at central nervous system: A Case Report and Literature Review. Case Rep Hematol. 2017;2017:9583257. doi: 10.1155/2017/9583257.
  41. 41. González-Bonet LG, García-Boyero R, Gaona-Morales J. Mantle cell lymphoma with central nervous system involvement simulating bilateral subdural hematomas. World Neurosurg. 2017;99:808. doi: 10.1016/j.wneu.2016.12.122.
  42. 42. Shaikh H, Jani P, Shah R, et al. Mantle cell lymphoma relapsing as disease of skin, orbit and CNS: an extremely rare presentation and a review of literature. J Hematol. 2018;7(1):38–42. doi: 10.14740/jh363w.
  43. 43. Vitagliano O, Trastulli F, Cacace F, et al. Ibrutinib as salvage therapy in mantle cell lymphoma with central nervous system involvement in a pretreated unfit patient. Leuk Lymphoma. 2018;59(7):1734–7. doi: 10.1080/10428194.2017.1387910.
  44. 44. Alsuliman T, Belghoul M, Choufi B. Ibrutinib treatment through nasogastric tube in a comatose patient with central nervous system localization of mantle cell lymphoma. Case Rep Hematol. 2018;2018:5761627. doi: 10.1155/2018/5761627.
  45. 45. Okahashi N, Uchihara M, Hoshino E. Mantle cell lymphoma with central nervous system relapse successfully treated with nasogastric-tube administration of ibrutinib. Rinsho Ketsueki. 2020;61(10):1508–10. doi: 10.11406/rinketsu.61.1508.
  46. 46. Nakamura M, Iwasa H, Kojima K. Central nervous system involvement in mantle cell lymphoma presenting magnetic resonance imaging features of mild encephalitis/encephalopathy with a reversible splenial lesion. Intern Med. 2021;60(10):1597–600. doi: 10.2169/internalmedicine.6386-20.
  47. 47. Ağargün BF, Özbalak M, Gülseren UA, et al. Central nervous system involvement of mantle cell lymphoma: Case report and review of the literature. Hematol Transfus Cell Ther. 2024;46(Suppl 6):S367–S372. doi: 10.1016/j.htct.2022.10.002.
  48. 48. Myers AL, Kawedia JD, Nader A, et al. A rare case of methotrexate and primaquine co-administration in a mantle cell lymphoma patient. J Clin Pharm Ther. 2019;44(5):800–4. doi: 10.1111/jcpt.12849.
  49. 49. Rich JD, Clark SM, Fedoriw Y, et al. Complete remission with ibrutinib after allogeneic stem cell transplant for central nervous system relapse of mantle cell lymphoma: A case report and literature review. Clin Case Rep. 2019;7(10):1957–61. doi: 10.1002/ccr3.2257.
  50. 50. Fukushima N, Mino T, Arihiro K, Ichinohe T. Cooccurrence of CD10-Positive and CD10-Negative Mantle Cell Lymphoma Complicated With Central Nervous System Involvement Solely by CD10-Positive Population. Cureus. 2022;14(1):e21341. doi: 10.7759/cureus.21341.
  51. 51. Rusconi C, Cheah CY, Tucker D, et al. Ibrutinib Compared to Immune-Chemotherapy for Central Nervous System Relapse of Mantle Cell Lymphoma: A Report from Fondazione Italiana Linfomi (FIL) and European Mantle Cell Lymphoma Network (EMCLN). HemaSphere. 2020;4(1):73–7. doi: 10.1182/blood.2022015560.
  52. 52. Hansen MH, Juul-Jensen K, Cédile O, et al. Distal chromosome 1q aberrations and initial response to ibrutinib in central nervous system relapsed mantle cell lymphoma. Leuk Res Rep. 2021;15:100255. doi: 10.1016/j.lrr.2021.100255.
  53. 53. Oh TS, Burkart M, Behdad A, et al. Ibrutinib plus R-ICE induces remission in blastoid variant mantle cell lymphoma with CNS relapse. Case Rep Hematol. 2022;2022:1930546. doi: 10.1155/2022/1930546.
  54. 54. Rusconi C, Cheah CY, Eyre TA, et al. Ibrutinib improves survival compared to chemotherapy in mantle cell lymphoma with central nervous system relapse. Blood. 2022;140(17):1907–16. doi: 10.1182/blood.2022015560.
  55. 55. McLaughlin N, Wang Y, Inwards DJ, et al. Outcomes in mantle cell lymphoma with central nervous system involvement. J Clin Oncol. 2021;39(15): Abstract e19527.
  56. 56. McLaughlin N, Wang Y, Witzig T, et al. Central nervous system involvement by mantle cell lymphoma. Leuk Lymphoma. 2023;64(2):371–7. doi: 10.1080/10428194.2022.2148211.
  57. 57. McLaughlin N, Joseph A, Wang Y, et al. Outcomes in Mantle Cell Lymphoma with Central Nervous System Involvement–a Dual Center Study. Blood. 2023;142(1):1670. doi: 10.1182/blood-2023-174701.
  58. 58. Vu K, Frank MJ. CAR T-cell therapy for mantle cell lymphoma with central nervous system relapse. Blood Adv. 2023;7(3):375–8. doi: 10.1182/bloodadvances.2022008031.
  59. 59. Rai M, Maziarz R, Ratterree B, et al. Relapsed mantle cell lymphoma with parenchymal central nervous system involvement successfully treated with chimeric antigen receptor T-cell therapy—a case report. Ann Lymphoma. 2024;8:1–6. doi: 10.21037/aol-23-22.
  60. 60. Chappelow AV, Singh AD, Perez VL, et al. Bilateral panocular involvement with mantle-cell lymphoma. J Clin Oncol. 2008;26(7):1167. doi: 10.1200/JCO.2007.14.2620.
  61. 61. Aldrees, S, Jeeva-Patel T, Margolin E. Bilateral infiltrative optic neuropathy of systemic mantle cell lymphoma. Can J Neurol Sci. 2020;47(3):428–30. doi: 10.1017/cjn.2020.28.
  62. 62. Small L, Ma C, Shah M et al. Bilateral vision loss as the initial presentation for central nervous system involvement of mantle cell lymphoma: A case series. Am J Ophthalmol Case Rep. 2021;23:101131. doi: 10.1016/j.ajoc.2021.101131.
  63. 63. Singer JR, Nigalye AK, Champion MT, Welch MJ. Intravitreal methotrexate for mantle cell lymphoma infiltration of the optic nerves: a case report. Retin Cases Brief Rep. 2018;12(1):5–9. doi: 10.1097/ICB.0000000000000385.
  64. 64. Jain P, Zhang S, Kanagal-Shamanna R, et al. Genomic profiles and clinical outcomes of de novo blastoid/pleomorphic MCL are distinct from those of transformed MCL. Blood Adv. 2020;4(6):1038–50. doi: 10.1182/bloodadvances.2019001396.
  65. 65. Fischer L, Korfel A, Pfeiffer S, et al CXCL13 and CXCL12 in central nervous system lymphoma patients. Clin Cancer Res. 2009;15(19):5968–73. doi: 10.1158/1078-0432.CCR-09-0108.
  66. 66. Smith JR, Falkenhagen KM, Coupland SE, et al. Malignant B cells from patients with primary central nervous system lymphoma express stromal cell-derived factor-1. Am J Clin Pathol. 2007;127(4):633–41. doi: 10.1309/NUQHJ79BHWYD9TAF.
  67. 67. Rubenstein JL, Wong VS, Kadoch C, et al. CXCL13 plus interleukin 10 is highly specific for the diagnosis of CNS lymphoma. Blood. 2013;121(23):4740–8. doi: 10.1182/blood-2013-01-476333.
  68. 68. Bashir, R. Coakham H, Hochberg F. Expression of LFA-1/ICAM-1 in CNS lymphomas: possible mechanism for lymphoma homing into the brain. J Neurooncol. 1992;12(2):103–10. doi: 10.1007/BF00172658.
  69. 69. Moller P, Eichelmann A, Koretz K, Mechtersheimer G. Adhesion molecules VLA-1 to VLA-6 define discrete stages of peripheral B lymphocyte development and characterize different types of B cell neoplasia. Leukemia. 1992;6(4):256–64.
  70. 70. Terol MJ, Lopez-Guillermo A, Bosch F, et al. Expression of beta-integrin adhesion molecules in non-Hodgkin’s lymphoma: correlation with clinical and evolutive features. J Clin Oncol. 1999;17(6):1869–75. doi: 10.1200/JCO.1999.17.6.1869.
  71. 71. Angelopoulou MK, Kontopidou GA, Pangalis FN. Adhesion molecules in B-chronic lymphoproliferative disorders. Semin Hematol. 1999;36(2):178–97.
  72. 72. Rubenstein JL, Fridlyand J, Shen A, et al. Gene expression and angiotropism in primary CNS lymphoma. Blood. 2006;107(9):3716–23. doi: 10.1182/blood-2005-03-0897.
  73. 73. Kim M, Kizilbash SH, Laramy JK, et al. Barriers to effective drug treatment for brain metastases: a multifactorial problem in the delivery of precision medicine. Pharm Res. 2018;35(9):177. doi: 10.1007/s11095-018-2455-9.
  74. 74. Bechmann I, Galea I, Perry VH. What is the blood-brain barrier (not)? Trends Immunol. 2007;28(1):5–11. doi: 10.1016/j.it.2006.11.007.
  75. 75. Pardridge WM. Delivery of biologics across the blood-brain barrier with molecular Trojan horse technology. BioDrugs. 2017;31(6):503–19. doi: 10.1007/s40259-017-0248-z.
  76. 76. Gampa G, Vaidhyanathan S, Sarkaria JN, Elmquist WF. Drug delivery to melanoma brain metastases: can current challenges lead to new opportunities? Pharmacol Res. 2017;123:10–25. doi: 10.1016/j.phrs.2017.06.008.
  77. 77. Medesan C, Radu C, Kim JK, et al. Localization of the site of the IgG molecule that regulates maternofetal transmission in mice. Eur J Immunol. 1996;26(10):2533–6. doi: 10.1002/eji.1830261038.
  78. 78. Wang W, Wang EQ, Balthasar JP. Monoclonal antibody pharmacokinetics and pharmacodynamics. Clin Pharmacol Ther. 2008;84(5):548–58. doi: 10.1038/clpt.2008.170.
  79. 79. Scott-Taylor TH, Axinia SC, Amin S, et al. Immunoglobulin G; structure and functional implications of different subclass modifications in initiation and resolution of allergy. Immunity Inflamm Dis. 2018;6(1):13–33. doi: 10.1002/iid3.192.
  80. 80. Pluim D, Ros W, Van Bussel MTJ, et al. Enzyme linked immunosorbent assay for the quantification of nivolumab and pembrolizumab in human serum and cerebrospinal fluid. J Pharm Biomed Anal. 2018;164:128–34. doi: 10.1016/j.jpba.2018.10.025.
  81. 81. Muscal JA, Sun Y, Nuchtern JG, et al. Plasma and cerebrospinal fluid pharmacokinetics of thalidomide and lenalidomide in nonhuman primates. Cancer Chemother Pharmacol. 2012;69(4):943–7. doi: 10.1007/s00280-011-1781-y.
  82. 82. Warren KE, Goldman S, Pollack IF, et al. Phase I trial of lenalidomide in pediatric patients with recurrent, refractory, or progressive primary CNS tumors: Pediatric Brain Tumor Consortium study PBTC-018. J Clin Oncol. 2011;29(3):324–9. doi: 10.1200/JCO.2010.31.3601.
  83. 83. Rubenstein JL, Treseler PA, Stewart PJ. Regression of refractory intraocular large B-cell lymphoma with lenalidomide monotherapy. J Clin Oncol. 2011;29(20):595–7. doi: 10.1200/JCO.2011.34.7252.
  84. 84. Rubenstein JL, Rosenberg J, Damon L. High-dose methotrexate plus rituximab (Anti-CD20) monoclonal antibody in the treatment of primary CNS lymphoma. Society for Neuro-Oncology 4th annual meeting, Scottsdale, AZ; 1999. Abstract.
  85. 85. Harjunpää A, Wiklund T, Collan J, et al. Complement activation in circulation and central nervous system after rituximab (anti-CD20) treatment of B-cell lymphoma. Leuk Lymphoma. 2001;42(4):731–8. doi: 10.3109/10428190109099335.
  86. 86. Yip V, Lee MV, Saad OM, et al. Preclinical characterization of the distribution, catabolism, and elimination of a Polatuzumab Vedotin-Piiq (POLIVY®) antibody–drug conjugate in sprague dawley rats. J Clin Med. 2021;10(6):1323. doi: 10.3390/jcm10061323.
  87. 87. Yu H, Kong H, Li C, et al. Bruton’s tyrosine kinase inhibitors in primary central nervous system lymphoma-evaluation of anti-tumor efficacy and brain distribution. Transl Cancer Res. 2021;10(5):1975–83. doi: 10.21037/tcr-21-50.
  88. 88. Australia T.G.A. Australian Public Assessment Report for Acalabrutinib. Health Do. 2024. Available from: https://www.tga.gov.au/auspar/auspar-acalabrutinib (accessed 28.05.2024).
  89. 89. Barrett A, Eyre TA, Bhuva S, et al. Complete response of mantle cell lymphoma with central nervous system involvement at diagnosis with acalabrutinib – Case report. EJHaem. 2023;5(1):238–41. doi: 10.1002/jha2.830.
  90. 90. Rios A, Rekoff G, Dinh B, et al. MCL-247: durable response of a patient with a mantle cell lymphoma central nervous system (CNS) relapse to treatment with a Bruton tyrosine kinase inhibitor (BTKi) monotherapy. Clin Lymphoma Myeloma Leuk. 2020;20(1):259–60. doi: 10.1016/S2152-2650(20)30862-4.
  91. 91. Yohannan B, Sridhar A, Nguyen N, et al. Durable remission with Bruton’s tyrosine kinase inhibitor therapy in a patient with leptomeningeal disease secondary to relapsed mantle cell lymphoma. BMJ Case Rep. 2022;15(6):e249631. doi: 10.1136/bcr-2022-249631.
  92. 92. Reda G, Cassin R, Dovrtelova G, et al. Venetoclax penetrates in cerebrospinal fluid and may be effective in chronic lymphocytic leukemia with central nervous system involvement. Haematologica. 2019;104(5):222–3. doi: 10.3324/haematol.2018.213157.
  93. 93. Ahmed G, Alsouqi A, Szabo A, et al. CAR T-cell therapy in mantle cell lymphoma with secondary CNS involvement: a multicenter experience. Blood Adv. 2024;8(13):3528–31. doi: 10.1182/bloodadvances.2023012255.
  94. 94. Zhang Y, Li Y, Zhuang Z, et al. Preliminary evaluation of zanubrutinib-containing regimens in DLBCL and the cerebrospinal fluid distribution of zanubrutinib: a 13-case series. Front Oncol. 2021;11:760405. doi: 10.3389/fonc.2021.760405.
  95. 95. FDA Approved Drug Products: JAYPIRCA (pirtobrutinib) tablets for oral use. Available from: https://pi.lilly.com/us/jaypirca-uspi.pdf?s=pi (accessed 30.09.2024).
  96. 96. Zhang Y, Wang W, Zhao D, et al. Preliminary results of a phase II study of orelabrutinib in combination with anti-PD-1 monoclonal antibody in refractory or relapsed primary CNS lymphoma. HemaSphere. 2022;6(S3):256–7.
  97. 97. Liston DR, Davis M. Clinically relevant concentrations of anticancer drugs: a guide for nonclinical studies. Clin Cancer Res. 2017;23(14):3489–98. doi: 10.1158/1078-0432.CCR-16-3083.
  98. 98. Rubenstein JL, Combs D, Rosenberg J, et al. Rituximab therapy for CNS lymphomas: Targeting the leptomeningeal compartment. Blood. 2003;101(2):466–8. doi: 10.1182/blood-2002-06-1636.
  99. 99. Kizhedath A, Wilkinson S, Glassey J. Applicability of traditional in vitro toxicity tests for assessing adverse effects of monoclonal antibodies: A case study of rituximab and trastuzumab. Antibodies. 2018;7(3):30. doi: 10.3390/antib7030030.
  100. 100. Zhai J, Qin Y, Zhu J, et al. Pharmacokinetics of obinutuzumab in Chinese patients with B-cell lymphomas. Br J Clin Pharmacol. 2017;83(7):1446–56. doi: 10.1111/bcp.13232.
  101. 101. US Food and Drug Administration (FDA). FDA drug safety communication: FDA approval of Polivy (polatuzumab vedotin-piiq) for previously untreated diffuse large B-cell lymphoma, not otherwise specified, and high-grade B-cell lymphoma. Available from: https://www.fda.gov/drugs/resources-information-approved-drugs/fda-disco-burst-edition-fda-approval-polivy-polatuzumab-vedotin-piiq-previously-untreated-diffuse (accessed 30.09.2024).
  102. 102. Yip V, Lee MV, Saad OM, et al. Preclinical characterization of the distribution, catabolism, and elimination of a polatuzumab vedotin-piiq (Polivy®) antibody–drug conjugate in sprague dawley rats. J Clin Med. 2021;10(6):1323. doi: 10.3390/jcm10061323.
  103. 103. Shemesh CS, et al. Pharmacokinetics of polatuzumab vedotin in combination with R/G-CHP in patients with B-cell non-Hodgkin lymphoma. Cancer Chemother Pharmacol. 2020;85(5):831–42. doi: 10.1007/s00280-020-04054-8.
  104. 104. Salem AH, Badawi MA, Place AE, et al. Venetoclax crosses the blood brain barrier: a pharmacokinetic analysis of the cerebrospinal fluid in pediatric leukemia patients. Blood. 2020;136(Suppl 1):30–1. doi: 10.1182/blood-2020-137197.
  105. 105. Badawi M, Menon R, Place AE, et al. Venetoclax Penetrates the Blood Brain Barrier: A Pharmacokinetic Analysis in Pediatric Leukemia Patients. J Cancer. 2023;14(7):1151–6. doi: 10.7150/jca.81795.
  106. 106. Portnow J, Wang D, Blanchard MS, et al. Systemic Anti-PD-1 immunotherapy results in PD-1 blockade on T cells in the cerebrospinal fluid. JAMA Oncol. 2020;6(12):1947–51. doi: 10.1001/jamaoncol.2020.4508.
  107. 107. Shirley M. Glofitamab: first approval. Drugs. 2023;83(10):935–91. doi: 10.1007/s40265-023-01894-5.
  108. 108. Godfrey JK, Gao L, Shouse G, et al. Glofitamab stimulates immune cell infiltration of CNS tumors and induces clinical responses in secondary CNS lymphoma. Blood. 2024;144(4):457–61. doi: 10.1182/blood.2024024168.
  109. 109. Tecartus (brexucabtagene autoleucel) [package insert]. Santa Monica: Kite Pharma Inc; April 2024. Available from: https://www.gilead.com/-/media/files/pdfs/medicines/oncology/tecartus/tecartus-pi.pdf (accessed 30.09.2024).
  110. 110. Siddiqi T, Wang X, Blanchard MS, et al. CD19-directed CAR T-cell therapy for treatment of primary CNS lymphoma. Blood Adv. 2021;5(20):4059–63. doi: 10.1182/bloodadvances.2020004106.
  111. 111. Ogasawara K, Lymp J, Mack T, et al. In vivo cellular expansion of lisocabtagene maraleucel and association with efficacy and safety in relapsed/refractory large B-cell lymphoma. Clin Pharmacol Ther. 2022;112(1):81–9. doi: 10.1002/cpt.2561.
Лицензия Creative Commons

Это произведение доступно по лицензии Creative Commons «Attribution-NonCommercial-ShareAlike» («Атрибуция — Некоммерческое использование — На тех же условиях») 4.0 Всемирная.

Copyright (c) 2025 Клиническая онкогематология