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Incidence, management, and outcomes of autoimmune nephropathies following alemtuzumab treatment in patients with multiple sclerosis

. 2019 Aug ; 25 (9) : 1273-1288. [epub] 20190415

Language English Country Great Britain, England Media print-electronic

Document type Journal Article, Research Support, Non-U.S. Gov't

Grant support
G1100114 Medical Research Council - United Kingdom

BACKGROUND: Autoimmune disorders including nephropathies have been reported more frequently in alemtuzumab-treated multiple sclerosis (MS) patients than in the general population. OBJECTIVE: Describe instances of autoimmune nephropathy in alemtuzumab-treated MS patients. METHODS: Cases were identified from safety monitoring within the alemtuzumab relapsing-remitting multiple sclerosis (RRMS) clinical development program (CDP) or post-marketing, or following off-label use. RESULTS: As of 16 June 2017, 16 autoimmune nephropathies have occurred following alemtuzumab treatment for MS. The incidence of autoimmune nephropathies was 0.34% within the CDP (5/1485 patients). The five CDP cases (one of anti-glomerular basement membrane (anti-GBM) disease, two of membranous glomerulonephropathy, and two of serum anti-GBM antibody without typical anti-GBM disease) were identified early, responded to conventional therapy (where needed), and had favorable outcomes. Three of 11 cases outside the CDP occurred following off-label alemtuzumab use prior to approval for RRMS and were all anti-GBM disease. Diagnosis was delayed in one of these three cases and another did not receive appropriate treatment; all three cases resulted in end-stage renal failure. All anti-GBM disease cases with documented urinalysis demonstrated prior microscopic hematuria. CONCLUSION: Close monitoring of alemtuzumab-treated MS patients facilitates diagnosis and treatment early in the nephropathy course when preservation of renal function is more likely.

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Coles AJ, Cox A, Le Page E, et al. The window of therapeutic opportunity in multiple sclerosis: Evidence from monoclonal antibody therapy. J Neurol 2006; 253(1): 98–108. PubMed

Coles AJ, Compston DA, Selmaj KW, et al. Alemtuzumab vs. interferon beta-1a in early multiple sclerosis. N Engl J Med 2008; 359(17): 1786–1801. PubMed

Cohen JA, Coles AJ, Arnold DL, et al. Alemtuzumab versus interferon beta 1a as first-line treatment for patients with relapsing-remitting multiple sclerosis: A randomised controlled phase 3 trial. Lancet 2012; 380(9856): 1819–1828. PubMed

Coles AJ, Twyman CL, Arnold DL, et al. Alemtuzumab for patients with relapsing multiple sclerosis after disease-modifying therapy: A randomised controlled phase 3 trial. Lancet 2012; 380(9856): 1829–1839. PubMed

Meyer D, Coles A, Oyuela P, et al. Case report of antiglomerular basement membrane disease following alemtuzumab treatment of relapsing-remitting multiple sclerosis. Mult Scler Rel Disord 2013; 2: 60–63. PubMed

Wynn DR, Arnold DL, Coles A, et al. Detection, incidence, and management of glomerulonephritis in the alemtuzumab clinical development program. Mult Scler 2013; 19: P597.

Perazella MA. Drug-induced nephropathy: An update. Expert Opin Drug Saf 2005; 4: 689–706. PubMed

Havrdova E, Arnold DL, Cohen JA, et al. Alemtuzumab CARE-MS I 5-year follow-up: Durable efficacy in the absence of continuous MS therapy. Neurology 2017; 89: 1107–1116. PubMed PMC

Coles AJ, Cohen JA, Fox EJ, et al. Alemtuzumab CARE-MS II 5-year follow-up: Efficacy and safety findings. Neurology 2017; 89: 1117–1126. PubMed PMC

Coles AJ, Fox E, Vladic A, et al. Alemtuzumab more effective than interferon beta-1a at 5-year follow-up of CAMMS223 clinical trial. Neurology 2012; 78: 1069–1078. PubMed

Osterborg A, Mellstedt H, Keating M. Clinical effects of alemtuzumab (Campath-1H) in B-cell chronic lymphocytic leukemia. Med Oncol 2002; 19(Suppl.): S21–S26. PubMed

Walsh M, Chaudhry A, Jayne D. Long-term follow-up of relapsing/refractory anti-neutrophil cytoplasm antibody associated vasculitis treated with the lymphocyte depleting antibody alemtuzumab (CAMPATH-1H). Ann Rheum Dis 2008; 67(9): 1322–1327. PubMed

Friend PJ. Alemtuzumab induction therapy in solid organ transplantation. Transplant Res 2013; 2(Suppl. 1): S5. PubMed PMC

Cull GM, Haynes AP, Byrne JL, et al. Preliminary experience of allogeneic stem cell transplantation for lymphoproliferative disorders using BEAM-CAMPATH conditioning: An effective regimen with low procedure-related toxicity. Br J Haematol 2000; 108(4): 754–760. PubMed

Genzyme Therapeutics Ltd. Lemtrada™ (alemtuzumab 12 mg concentrate for solution for infusion). EU summary of product characteristics, https://www.ema.europa.eu/en/documents/product-information/lemtrada-epar-product-information_en.pdf (2018, accessed 12 February 2018).

Sanofi Genzyme. Prescribing information. Lemtrada™ (alemtuzumab), for intravenous injection. Cambridge, MA: Sanofi Genzyme, 2017.

Hu Y, Turner MJ, Shields J, et al. Investigation of the mechanism of action of alemtuzumab in a human CD52 transgenic mouse model. Immunology 2009; 128(2): 260–270. PubMed PMC

Rao SP, Sancho J, Campos-Rivera J, et al. Human peripheral blood mononuclear cells exhibit heterogeneous CD52 expression levels and show differential sensitivity to alemtuzumab mediated cytolysis. PLoS ONE 2012; 7(6): e39416. PubMed PMC

Turner MJ, Lamorte MJ, Chretien N, et al. Immune status following alemtuzumab treatment in human CD52 transgenic mice. J Neuroimmunol 2013; 261(1–2): 29–36. PubMed

De Mercanti S, Rolla S, Cucci A, et al. Alemtuzumab long-term immunologic effect: Treg suppressor function increases up to 24 months. Neurol Neuroimmunol Neuroinflamm 2016; 3: e194. PubMed PMC

Fox EJ. Alemtuzumab in the treatment of relapsing-remitting multiple sclerosis. Expert Rev Neurother 2010; 10: 1789–1797. PubMed

Freedman MS, Kaplan JM, Markovic-Plese S. Insights into the mechanisms of the therapeutic efficacy of alemtuzumab in multiple sclerosis. J Clin Cell Immunol 2013; 4(4): 1000152. PubMed PMC

Coles AJ, Boyko AN, De Seze J, et al. Alemtuzumab durably improves clinical outcomes in patients with active RRMS in the absence of continuous treatment: 7-year follow-up of CARE-MS I patients (TOPAZ study). Mult Scler 2017; 23(Suppl. 3): P1188.

Arnold DL, Barnett M, Comi G, et al. Durable reduction in MRI disease activity and slowing of brain volume loss with alemtuzumab in patients with active RRMS: 7-year follow-up of CARE-MS I patients (TOPAZ study). Mult Scler 2017; 23(Suppl. 3): P1189.

Singer BA, Alroughani R, Brassat D, et al. Durable improvements in clinical outcomes with alemtuzumab in patients with active RRMS in the absence of continuous treatment: 7-year follow-up of CARE-MS II patients (TOPAZ study). Mult Scler 2017; 23(Suppl. 3): P736.

Pelletier D, Traboulsee A, Barnett M, et al. Patients with active RRMS experience durable reductions in MRI disease activity and slowing of brain volume loss with alemtuzumab: 7-year follow-up of CARE-MS II patients (TOPAZ study). Mult Scler 2017; 23(Suppl. 3): P741.

Ziemssen T, Thomas K. Alemtuzumab in the long-term treatment of relapsing-remitting multiple sclerosis: An update on the clinical trial evidence and data from the real world. Ther Adv Neurol Disord 2017; 10(10): 343–359. PubMed PMC

Sanofi Genzyme. Lemtrada™ REMS (Risk Evaluation and Mitigation Strategy) program. Cambridge, MA: Sanofi Genzyme, 2017.

Brinar V, Giovannoni G, Havrdova E, et al. A phase 3b/4 long-term study of alemtuzumab in patients with relapsing-remitting multiple sclerosis: TOPAZ study design. Neurology 2015; 84: P7219.

Clatworthy MR, Wallin EF, Jayne DR. Anti-glomerular basement membrane disease after alemtuzumab. N Engl J Med 2008; 359: 768–769. PubMed

Phelps RG, Rees AJ. The HLA complex in Goodpasture’s disease: A model for analyzing susceptibility to autoimmunity. Kidney Int 1999; 56(5): 1638–1653. PubMed

Hollenbach JA, Oksenberg JR. The immunogenetics of multiple sclerosis: A comprehensive review. J Autoimmun 2015; 64: 13–25. PubMed PMC

Selmaj KW, Habek M, Bass A, et al. Efficacy and safety of alemtuzumab in patients with RRMS is durable over 10 years: Follow-up from the CAMMS223 study. Neurology 2017; 88: P5338.

Turner N, Rees AJ. Antiglomerular basement disease. In: Davison AM, Cameron JS, Grunfeld JP, et al. (eds) Oxford textbook of clinical nephrology. 3rd ed. New York: Oxford University Press, 2005.

Henderson RD, Saltissi D, Pender MP. Goodpasture’s syndrome associated with multiple sclerosis. Acta Neurol Scand 1998; 98(2): 134–135. PubMed

Henderson RD, Bain CJ, Pender MP. The occurrence of autoimmune diseases in patients with multiple sclerosis and their families. J Clin Neurosci 2000; 7(5): 434–437. PubMed

Irizar H, Munoz-Culla M, Zuriarrain O, et al. HLA-DRB1*15:01 and multiple sclerosis: A female association? Mult Scler 2012; 18(5): 569–577. PubMed

Deegens JK, Wetzels JF. Diagnosis and treatment of primary glomerular diseases. Membranous nephropathy, focal segmental glomerulosclerosis and IgA nephropathy. Minerva Urol Nefrol 2005; 57: 211–236. PubMed

Hofstra JM, Wetzels JF. Management of patients with membranous nephropathy. Nephrol Dial Transplant 2012; 27(1): 6–9. PubMed

Campos A, Gieron MA, Gunasakeran S, et al. Membranous nephropathy associated with multiple sclerosis. Pediatr Neurol 1993; 9(1): 64–66. PubMed

Jones JL, Thompson SA, Loh P, et al. Human autoimmunity after lymphocyte depletion is caused by homeostatic T-cell proliferation. Proc Natl Acad Sci U S A 2013; 110(50): 20200–20205. PubMed PMC

Krupica T, Jr, Fry TJ, Mackall CL. Autoimmunity during lymphopenia: A two-hit model. Clin Immunol 2006; 120: 121–128. PubMed

Daniels GH, Vladic A, Brinar V, et al. Alemtuzumab-related thyroid dysfunction in a phase 2 trial of patients with relapsing-remitting multiple sclerosis. J Clin Endocrinol Metab 2014; 99(1): 80–89. PubMed

Phelps RG, Turner AN. Antiglomerular basement membrane disease and Goodpasture’s disease. In: Floege J, Johnson R, Feehally J. (eds.) Comprehensive clinical nephrology. 4th ed. St. Louis, MO: Saunders, 2010, pp. 282–291.

Zuvich RL, McCauley JL, Pericak-Vance MA, et al. Genetics and pathogenesis of multiple sclerosis. Semin Immunol 2009; 21: 328–333. PubMed PMC

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