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Adcetris - Acontecimiento adverso

▼ Adcetris®

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Neuropatía periférica

La neuropatía inducida por quimioterapia (NIQ) es la complicación neurológica más frecuente en el paciente onco-hematológico1-5.

  • Numerosos agentes antineoplásicos empleados en población adulta pueden inducir neuropatía periférica durante el tratamiento1-5

El diagnóstico de la neuropatía inducida por quimioterapia es principalmente clínico apoyado por exploraciones complementarias1,6,7.

Tres tipos de neuropatía periférica

Brentuximab vedotina provoca tres tipos de neuropatía periférica por afectación de los diferentes tipos de fibras nerviosas8-18.

  • NP Sensitiva8-10
  • NP Motora8-13
  • NP Autonomica8,14,15,18

La neuropatía periférica puede aparecer durante el tratamiento con brentuximab vedotina, habitualmente como consecuencia de la exposición acumulada14,16,19-22.

La neuropatía periférica inducida por brentuximab vedotina es manejable mediante modificación de dosis23.

En estudios de vida real se ha podido observar que la mayoría de los casos de neuropatía provocada por brentuximab vedotina en monoterapia fueron de intensidad leve y reversible con un manejo adecuado de la misma24,25.

Referencias

  1. Velasco R, Bruna J. Chemotherapy-induced peripheral neuropathy: An unresolved issue. Neurol (Engl Ed). 2010;25(2):116–31. Disponible en: http://dx.doi.org/10.1016/s2173-5808(10)70022-5
  2. Velasco R, Alemany M, Villagrán M, Argyriou AA. Predictive biomarkers of oxaliplatin-induced peripheral neurotoxicity. J Pers Med. 2021;11(7):669. Disponible en: http://dx.doi.org/10.3390/jpm11070669
  3. Smith EML, Kuisell C, Cho Y, Kanzawa-Lee GA, Gilchrist LS, Park SB, et al. Characteristics and patterns of pediatric chemotherapy-induced peripheral neuropathy: A systematic review. Cancer Treat Res Commun. 2021;28(100420):100420. Disponible en: http://dx.doi.org/10.1016/j.ctarc.2021.100420
  4. Velasco R, Alberti P, Bruna J, Psimaras D, Argyriou AA. Bortezomib and other proteosome inhibitors-induced peripheral neurotoxicity: From pathogenesis to treatment. J Peripher Nerv Syst. 2019;24 (supl 2):S52–62. Disponible en: http://dx.doi.org/10.1111/jns.12338
  5. Argyriou AA, Bruna J, Mantovani E, Tamburin S. Neuromuscular complications of cancer therapy. Curr Opin Neurol. 2021;34(5):658–68. Disponible en: http://dx.doi.org/10.1097/WCO.0000000000000969
  6. Li T, Timmins HC, Lazarus HM, Park SB. Peripheral neuropathy in hematologic malignancies - Past, present and future. Blood Rev. 2020;43(100653):100653. Disponible en: http://dx.doi.org/10.1016/j.blre.2020.100653
  7. Argyriou AA, Park SB, Islam B, Tamburin S, Velasco R, Alberti P, et al. Neurophysiological, nerve imaging and other techniques to assess chemotherapy-induced peripheral neurotoxicity in the clinical and research settings. J Neurol Neurosurg Psychiatry. 2019;90(12):1361–9. Disponible en: http://dx.doi.org/10.1136/jnnp-2019-320969
  8. Mariotto S, Tecchio C, Sorio M, Bertolasi L, Turatti M, Tozzi MC, et al. Clinical and neurophysiological serial assessments of brentuximab vedotin-associated peripheral neuropathy. Leuk Lymphoma. 2019;60(11):2806–9. Disponible en: http://dx.doi.org/10.1080/10428194.2019.1605068
  9. Fargeot G, Dupel-Pottier C, Stephant M, Lazarovici J, Thomas L, Mouthon-Reignier C, et al. Brentuximab vedotin treatment associated with acute and chronic inflammatory demyelinating polyradiculoneuropathies. J Neurol Neurosurg Psychiatry. 2020;91(7):786–8. Disponible en: http://dx.doi.org/10.1136/jnnp-2020-323124
  10. Velasco R, Domingo-Domenech E, Sureda A. Brentuximab-induced peripheral neurotoxicity: A multidisciplinary approach to manage an emerging challenge in Hodgkin lymphoma therapy. Cancers (Basel). 2021;13(23):6125. Disponible en: http://dx.doi.org/10.3390/cancers13236125
  11. Mariotto S, Ferrari S, Sorio M, Benedetti F, Tridente G, Cavallaro T, et al. Brentuximab vedotin: axonal microtubule’s Apollyon. Blood Cancer J. 2015;5(8):e343. Disponible en: http://dx.doi.org/10.1038/bcj.2015.72
  12. Stone JB, DeAngelis LM. Cancer-treatment-induced neurotoxicity--focus on newer treatments. Nat Rev Clin Oncol. 2016;13(2):92–105. Disponible en: http://dx.doi.org/10.1038/nrclinonc.2015.152
  13. Pastorelli F, Derenzini E, Plasmati R, Pellegrini C, Broccoli A, Casadei B, et al. Severe peripheral motor neuropathy in a patient with Hodgkin lymphoma treated with brentuximab vedotin. Leuk Lymphoma. 2013;54(10):2318–21. Disponible en: http://dx.doi.org/10.3109/10428194.2013.773997
  14. Younes A, Gopal AK, Smith SE, Ansell SM, Rosenblatt JD, Savage KJ, et al. Results of a pivotal phase II study of brentuximab vedotin for patients with relapsed or refractory Hodgkin’s lymphoma. J Clin Oncol. 2012;30(18):2183–9. Disponible en: http://dx.doi.org/10.1200/JCO.2011.38.0410
  15. Clarivet B, Vincent L, Vergely L, Bres V, Foglia K, Cartron G, et al. Adverse reactions related to brentuximab vedotin use: A real-life retrospective study. Therapie. 2019;74(3):343–6. Disponible en: http://dx.doi.org/10.1016/j.therap.2018.07.004
  16. Moskowitz CH, Nademanee A, Masszi T, Agura E, Holowiecki J, Abidi MH, et al. Brentuximab vedotin as consolidation therapy after autologous stem-cell transplantation in patients with Hodgkin’s lymphoma at risk of relapse or progression (AETHERA): a randomised, double-blind, placebo-controlled, phase 3 trial. Lancet. 2015;385(9980):1853–62. Disponible en: http://dx.doi.org/10.1016/S0140-6736(15)60165-9
  17. Bartlett NL, Chen R, Fanale MA, Brice P, Gopal A, Smith SE, et al. Retreatment with brentuximab vedotin in patients with CD30-positive hematologic malignancies. J Hematol Oncol. 2014;7(1):24. Disponible en: http://dx.doi.org/10.1186/1756-8722-7-24
  18. Forero-Torres A, Holkova B, Goldschmidt J, Chen R, Olsen G, Boccia RV, et al. Phase 2 study of frontline brentuximab vedotin monotherapy in Hodgkin lymphoma patients aged 60 years and older. Blood. 2015;126(26):2798–804. Disponible en: http://dx.doi.org/10.1182/blood-2015-06-644336
  19. Corbin ZA, Nguyen-Lin A, Li S, Rahbar Z, Tavallaee M, Vogel H, et al. Characterization of the peripheral neuropathy associated with brentuximab vedotin treatment of Mycosis Fungoides and Sézary Syndrome. J Neurooncol. 2017;132(3):439–46. Disponible en: http://dx.doi.org/10.1007/s11060-017-2389-9
  20. Pro B, Advani R, Brice P, Bartlett NL, Rosenblatt JD, Illidge T, et al. Brentuximab vedotin (SGN-35) in patients with relapsed or refractory systemic anaplastic large-cell lymphoma: results of a phase II study. J Clin Oncol. 2012;30(18):2190–6. Disponible en: http://dx.doi.org/10.1200/JCO.2011.38.0402
  21. Fukuhara N, Yamamoto G, Tsujimura H, Chou T, Shibayama H, Yanai T, et al. Retreatment with brentuximab vedotin in patients with relapsed/refractory classical Hodgkin lymphoma or systemic anaplastic large-cell lymphoma: a multicenter retrospective study. Leuk Lymphoma. 2020;61(1):176–80. Disponible en: http://dx.doi.org/10.1080/10428194.2019.1654100
  22. Dummer R, Prince HM, Whittaker S, Horwitz SM, Kim YH, Scarisbrick J, et al. Patient-reported quality of life in patients with relapsed/refractory cutaneous T-cell lymphoma: Results from the randomised phase III ALCANZA study. Eur J Cancer. 2020;133:120–30. Disponible en: http://dx.doi.org/10.1016/j.ejca.2020.04.010
  23. Ficha técnica de Adcetris®. Junio 2022 [consultado marzo 2023]. Disponible en https://www.ema.europa.eu/en/documents/product-information/Adcetris-epar-product-information_es.pdf  
  24. Plattel WJ, Bergamasco A, Trinchese F, Gavini F, Bent-Ennakhil N, Zomas A, et al. Effectiveness of brentuximab vedotin monotherapy in relapsed or refractory Hodgkin lymphoma: a systematic review and meta-analysis. Leuk Lymphoma. 2021;62(14):3320–32. Disponible en: http://dx.doi.org/10.1080/10428194.2021.1957865
  25. Pellegrini C, Broccoli A, Pulsoni A, Rigacci L, Patti C, Gini G, et al. Italian real life experience with brentuximab vedotin: results of a large observational study on 234 relapsed/refractory Hodgkin’s lymphoma. Oncotarget. 2017;8(53):91703–10. Disponible en: http://dx.doi.org/10.18632/oncotarget.18114