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Published in: Current Dermatology Reports 4/2022

06-10-2022 | ANCA-Associated Vasculitis | Hospital-Based Dermatology (L Guggina and C Nguyen, Section Editors)

Off-Label Uses of Rituximab in Dermatology

Authors: Connor Cole, Kyle T. Amber

Published in: Current Dermatology Reports | Issue 4/2022

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Abstract

Purpose of Review

Rituximab has transformed the treatment of B-cell malignancies and rheumatoid arthritis in the past 2 decades. More recently, this anti-CD20 monoclonal antibody has seen increasing usage in the field of dermatology. This review highlights the evidence supporting its use in several important dermatologic conditions.

Recent Findings

Key recent findings include the 2018 FDA approval of rituximab for the treatment of moderate-to-severe pemphigus.

Summary

Data from randomized controlled trials have demonstrated the efficacy of rituximab in pemphigus, ANCA-associated vasculitis, and cryoglobulinemic vasculitis. More limited data suggests its use in recalcitrant cases of diseases such as pemphigoid, epidermolysis bullosa acquisita, and dermatomyositis. There is scarce evidence and mixed results for rituximab when studied in cutaneous polyarteritis nodosa and cutaneous lupus erythematosus.
Literature
1.
go back to reference Bhandari PR, Pai VV. Novel applications of rituximab in dermatological disorders. Indian Dermatol Online J. 2014;5(3):250–9.CrossRef Bhandari PR, Pai VV. Novel applications of rituximab in dermatological disorders. Indian Dermatol Online J. 2014;5(3):250–9.CrossRef
2.
go back to reference Gleghorn K, Wilson J, Wilkerson M. Rituximab: uses in dermatology. Skin Therapy Lett. 2016;21(5):5–7. Gleghorn K, Wilson J, Wilkerson M. Rituximab: uses in dermatology. Skin Therapy Lett. 2016;21(5):5–7.
3.
go back to reference Espana A, Ornilla E, Panizo C. Rituximab in dermatology. Actas Dermosifiliogr. 2013;104(5):380–92.CrossRef Espana A, Ornilla E, Panizo C. Rituximab in dermatology. Actas Dermosifiliogr. 2013;104(5):380–92.CrossRef
4.
go back to reference Hertl M, et al. Recommendations for the use of rituximab (anti-CD20 antibody) in the treatment of autoimmune bullous skin diseases. J Dtsch Dermatol Ges. 2008;6(5):366–73.CrossRef Hertl M, et al. Recommendations for the use of rituximab (anti-CD20 antibody) in the treatment of autoimmune bullous skin diseases. J Dtsch Dermatol Ges. 2008;6(5):366–73.CrossRef
5.
go back to reference Scheinfeld N. A review of rituximab in cutaneous medicine. Dermatol Online J. 2006;12(1):3.CrossRef Scheinfeld N. A review of rituximab in cutaneous medicine. Dermatol Online J. 2006;12(1):3.CrossRef
6.
go back to reference Carr DR, Heffernan MP. Off-label uses of in dermatology. Dermatol Ther. 2007;20(4):277–87.CrossRef Carr DR, Heffernan MP. Off-label uses of in dermatology. Dermatol Ther. 2007;20(4):277–87.CrossRef
7.
go back to reference Arin MJ, et al. Anti-CD20 monoclonal antibody (rituximab) in the treatment of pemphigus. Br J Dermatol. 2005;153(3):620–5.CrossRef Arin MJ, et al. Anti-CD20 monoclonal antibody (rituximab) in the treatment of pemphigus. Br J Dermatol. 2005;153(3):620–5.CrossRef
8.
go back to reference Esposito M, et al. Long-lasting remission of pemphigus vulgaris treated with rituximab. Acta Derm Venereol. 2006;86(1):87–9. Esposito M, et al. Long-lasting remission of pemphigus vulgaris treated with rituximab. Acta Derm Venereol. 2006;86(1):87–9.
9.
go back to reference Schmidt E, et al. Rituximab in refractory autoimmune bullous diseases. Clin Exp Dermatol. 2006;31(4):503–8.CrossRef Schmidt E, et al. Rituximab in refractory autoimmune bullous diseases. Clin Exp Dermatol. 2006;31(4):503–8.CrossRef
10.
go back to reference Maloney DG, et al. Phase I clinical trial using escalating single-dose infusion of chimeric anti-CD20 monoclonal antibody (IDEC-C2B8) in patients with recurrent B-cell lymphoma. Blood. 1994;84(8):2457–66.CrossRef Maloney DG, et al. Phase I clinical trial using escalating single-dose infusion of chimeric anti-CD20 monoclonal antibody (IDEC-C2B8) in patients with recurrent B-cell lymphoma. Blood. 1994;84(8):2457–66.CrossRef
11.
go back to reference Emer JJ, Claire W. Rituximab: a review of dermatological applications. J Clin Aesthet Dermatol. 2009;2(5):29–37. Emer JJ, Claire W. Rituximab: a review of dermatological applications. J Clin Aesthet Dermatol. 2009;2(5):29–37.
12.
go back to reference Ahmed AR, Shetty S. The emerging role of rituximab in autoimmune blistering diseases. Am J Clin Dermatol. 2015;16(3):167–77.CrossRef Ahmed AR, Shetty S. The emerging role of rituximab in autoimmune blistering diseases. Am J Clin Dermatol. 2015;16(3):167–77.CrossRef
13.
go back to reference Pollmann R, et al. Identification of autoreactive B cell subpopulations in peripheral blood of autoimmune patients with pemphigus vulgaris. Front Immunol. 2019;10:1375.CrossRef Pollmann R, et al. Identification of autoreactive B cell subpopulations in peripheral blood of autoimmune patients with pemphigus vulgaris. Front Immunol. 2019;10:1375.CrossRef
14.
go back to reference Tokunaga M, et al. Down-regulation of CD40 and CD80 on B cells in patients with life-threatening systemic lupus erythematosus after successful treatment with rituximab. Rheumatology. 2005;44(2):176–82.CrossRef Tokunaga M, et al. Down-regulation of CD40 and CD80 on B cells in patients with life-threatening systemic lupus erythematosus after successful treatment with rituximab. Rheumatology. 2005;44(2):176–82.CrossRef
15.
go back to reference Tokunaga M, et al. Efficacy of rituximab (anti-CD20) for refractory systemic lupus erythematosus involving the central nervous system. Ann Rheum Dis. 2007;66(4):470–5.CrossRef Tokunaga M, et al. Efficacy of rituximab (anti-CD20) for refractory systemic lupus erythematosus involving the central nervous system. Ann Rheum Dis. 2007;66(4):470–5.CrossRef
16.
go back to reference Sfikakis PP, et al. Remission of proliferative lupus nephritis following B cell depletion therapy is preceded by down-regulation of the T cell costimulatory molecule CD40 ligand: an open-label trial. Arthritis Rheum. 2005;52(2):501–13.CrossRef Sfikakis PP, et al. Remission of proliferative lupus nephritis following B cell depletion therapy is preceded by down-regulation of the T cell costimulatory molecule CD40 ligand: an open-label trial. Arthritis Rheum. 2005;52(2):501–13.CrossRef
17.
go back to reference Sfikakis PP, Boletis JN, Tsokos GC. Rituximab anti-B-cell therapy in systemic lupus erythematosus: pointing to the future. Curr Opin Rheumatol. 2005;17(5):550–7.CrossRef Sfikakis PP, Boletis JN, Tsokos GC. Rituximab anti-B-cell therapy in systemic lupus erythematosus: pointing to the future. Curr Opin Rheumatol. 2005;17(5):550–7.CrossRef
18.
go back to reference Desai-Mehta A, et al. Hyperexpression of CD40 ligand by B and T cells in human lupus and its role in pathogenic autoantibody production. J Clin Invest. 1996;97(9):2063–73.CrossRef Desai-Mehta A, et al. Hyperexpression of CD40 ligand by B and T cells in human lupus and its role in pathogenic autoantibody production. J Clin Invest. 1996;97(9):2063–73.CrossRef
19.
go back to reference Toubi E, et al. Changes in macrophage function after rituximab treatment in patients with rheumatoid arthritis. Ann Rheum Dis. 2007;66(6):818–20.CrossRef Toubi E, et al. Changes in macrophage function after rituximab treatment in patients with rheumatoid arthritis. Ann Rheum Dis. 2007;66(6):818–20.CrossRef
20.
go back to reference Vigna-Perez M, et al. Clinical and immunological effects of Rituximab in patients with lupus nephritis refractory to conventional therapy: a pilot study. Arthritis Res Ther. 2006;8(3):R83.CrossRef Vigna-Perez M, et al. Clinical and immunological effects of Rituximab in patients with lupus nephritis refractory to conventional therapy: a pilot study. Arthritis Res Ther. 2006;8(3):R83.CrossRef
21.
go back to reference Sfikakis PP, et al. Increased expression of the FoxP3 functional marker of regulatory T cells following B cell depletion with rituximab in patients with lupus nephritis. Clin Immunol. 2007;123(1):66–73.CrossRef Sfikakis PP, et al. Increased expression of the FoxP3 functional marker of regulatory T cells following B cell depletion with rituximab in patients with lupus nephritis. Clin Immunol. 2007;123(1):66–73.CrossRef
22.
go back to reference Vallerskog T, et al. Treatment with rituximab affects both the cellular and the humoral arm of the immune system in patients with SLE. Clin Immunol. 2007;122(1):62–74.CrossRef Vallerskog T, et al. Treatment with rituximab affects both the cellular and the humoral arm of the immune system in patients with SLE. Clin Immunol. 2007;122(1):62–74.CrossRef
23.
go back to reference Nagel A, et al. Rituximab mediates a strong elevation of B-cell-activating factor associated with increased pathogen-specific IgG but not autoantibodies in pemphigus vulgaris. J Invest Dermatol. 2009;129(9):2202–10.CrossRef Nagel A, et al. Rituximab mediates a strong elevation of B-cell-activating factor associated with increased pathogen-specific IgG but not autoantibodies in pemphigus vulgaris. J Invest Dermatol. 2009;129(9):2202–10.CrossRef
24.
go back to reference Maloney DG, et al. IDEC-C2B8 (rituximab) anti-CD20 monoclonal antibody therapy in patients with relapsed low-grade non-Hodgki’s lymphoma. Blood. 1997;90(6):2188–95.CrossRef Maloney DG, et al. IDEC-C2B8 (rituximab) anti-CD20 monoclonal antibody therapy in patients with relapsed low-grade non-Hodgki’s lymphoma. Blood. 1997;90(6):2188–95.CrossRef
25.
go back to reference Davies A, et al. Pharmacokinetics and safety of subcutaneous rituximab in follicular lymphoma (SABRINA): stage 1 analysis of a randomised phase 3 study. Lancet Oncol. 2014;15(3):343–52.CrossRef Davies A, et al. Pharmacokinetics and safety of subcutaneous rituximab in follicular lymphoma (SABRINA): stage 1 analysis of a randomised phase 3 study. Lancet Oncol. 2014;15(3):343–52.CrossRef
26.
go back to reference Roll P, et al. Regeneration of B cell subsets after transient B cell depletion using anti-CD20 antibodies in rheumatoid arthritis. Arthritis Rheum. 2006;54(8):2377–86.CrossRef Roll P, et al. Regeneration of B cell subsets after transient B cell depletion using anti-CD20 antibodies in rheumatoid arthritis. Arthritis Rheum. 2006;54(8):2377–86.CrossRef
27.
go back to reference Ng KP, et al. B cell depletion therapy in systemic lupus erythematosus: long-term follow-up and predictors of response. Ann Rheum Dis. 2007;66(9):1259–62.CrossRef Ng KP, et al. B cell depletion therapy in systemic lupus erythematosus: long-term follow-up and predictors of response. Ann Rheum Dis. 2007;66(9):1259–62.CrossRef
28.
go back to reference Rider LG, et al. Novel assessment tools to evaluate clinical and laboratory responses in a subset of patients enrolled in the rituximab in Myositis trial. Clin Exp Rheumatol. 2014;32(5):689–96. Rider LG, et al. Novel assessment tools to evaluate clinical and laboratory responses in a subset of patients enrolled in the rituximab in Myositis trial. Clin Exp Rheumatol. 2014;32(5):689–96.
29.
go back to reference • Joly P, et al. First-line rituximab combined with short-term prednisone versus prednisone alone for the treatment of pemphigus (Ritux 3): a prospective, multicentre, parallel-group, open-label randomised trial. Lancet. 2017;389(10083):2031–40. This important study from Joly et al demonstrated the superiority of rituximab plus steroids compared to steroid monotherapy in the treatment of pemphigus. This work was fundamental in rituximab being approved by the FDA in 2018 for the treatment of moderate-to-severe pemphigus. • Joly P, et al. First-line rituximab combined with short-term prednisone versus prednisone alone for the treatment of pemphigus (Ritux 3): a prospective, multicentre, parallel-group, open-label randomised trial. Lancet. 2017;389(10083):2031–40. This important study from Joly et al demonstrated the superiority of rituximab plus steroids compared to steroid monotherapy in the treatment of pemphigus. This work was fundamental in rituximab being approved by the FDA in 2018 for the treatment of moderate-to-severe pemphigus.
30.
go back to reference Fink-Puches R, et al. Treatment of primary cutaneous B-cell lymphoma with rituximab. J Am Acad Dermatol. 2005;52(5):847–53.CrossRef Fink-Puches R, et al. Treatment of primary cutaneous B-cell lymphoma with rituximab. J Am Acad Dermatol. 2005;52(5):847–53.CrossRef
31.
go back to reference Kerl K, et al. Intralesional and intravenous treatment of cutaneous B-cell lymphomas with the monoclonal anti-CD20 antibody rituximab: report and follow-up of eight cases. Br J Dermatol. 2006;155(6):1197–200.CrossRef Kerl K, et al. Intralesional and intravenous treatment of cutaneous B-cell lymphomas with the monoclonal anti-CD20 antibody rituximab: report and follow-up of eight cases. Br J Dermatol. 2006;155(6):1197–200.CrossRef
32.
go back to reference Martin SJ, Duvic M. Treatment of cutaneous lymphoid hyperplasia with the monoclonal anti-CD20 antibody rituximab. Clin Lymphoma Myeloma Leuk. 2011;11(3):286–8.CrossRef Martin SJ, Duvic M. Treatment of cutaneous lymphoid hyperplasia with the monoclonal anti-CD20 antibody rituximab. Clin Lymphoma Myeloma Leuk. 2011;11(3):286–8.CrossRef
33.
go back to reference Ahmed AR, Kaveri S. Reversing autoimmunity combination of rituximab and intravenous immunoglobulin. Front Immunol. 2018;9:1189.CrossRef Ahmed AR, Kaveri S. Reversing autoimmunity combination of rituximab and intravenous immunoglobulin. Front Immunol. 2018;9:1189.CrossRef
34.
go back to reference Kushner CJ, et al. Factors associated with complete remission after rituximab therapy for pemphigus. JAMA Dermatol. 2019;155(12):1404–9.CrossRef Kushner CJ, et al. Factors associated with complete remission after rituximab therapy for pemphigus. JAMA Dermatol. 2019;155(12):1404–9.CrossRef
35.
go back to reference Rashid H, et al. The effectiveness of rituximab in pemphigus and the benefit of additional maintenance infusions: daily practice data from a retrospective study. J Am Acad Dermatol. 2020;83(5):1503–5.CrossRef Rashid H, et al. The effectiveness of rituximab in pemphigus and the benefit of additional maintenance infusions: daily practice data from a retrospective study. J Am Acad Dermatol. 2020;83(5):1503–5.CrossRef
36.
go back to reference Tovanabutra N, et al. Temporal outcomes after rituximab therapy for pemphigus vulgaris. J Invest Dermatol. 2022;142(4):1058–64.CrossRef Tovanabutra N, et al. Temporal outcomes after rituximab therapy for pemphigus vulgaris. J Invest Dermatol. 2022;142(4):1058–64.CrossRef
37.
go back to reference You C, et al. Rituximab in the treatment of ocular cicatricial pemphigoid: a retrospective cohort study. Graefes Arch Clin Exp Ophthalmol. 2017;255(6):1221–8.CrossRef You C, et al. Rituximab in the treatment of ocular cicatricial pemphigoid: a retrospective cohort study. Graefes Arch Clin Exp Ophthalmol. 2017;255(6):1221–8.CrossRef
38.
go back to reference Hainsworth JD. Safety of rituximab in the treatment of B cell malignancies: implications for rheumatoid arthritis. Arthritis Res Ther. 2003;5(Suppl 4):S12–6.CrossRef Hainsworth JD. Safety of rituximab in the treatment of B cell malignancies: implications for rheumatoid arthritis. Arthritis Res Ther. 2003;5(Suppl 4):S12–6.CrossRef
39.
go back to reference Cheungpasitporn W, et al. Non-ischemic cardiomyopathy after rituximab treatment for membranous nephropathy. J Renal Inj Prev. 2017;6(1):18–25.CrossRef Cheungpasitporn W, et al. Non-ischemic cardiomyopathy after rituximab treatment for membranous nephropathy. J Renal Inj Prev. 2017;6(1):18–25.CrossRef
40.
go back to reference Linschoten M, et al. Cardiovascular adverse events in patients with non-Hodgkin lymphoma treated with first-line cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) or CHOP with rituximab (R-CHOP): a systematic review and meta-analysis. Lancet Haematol. 2020;7(4):e295–308.CrossRef Linschoten M, et al. Cardiovascular adverse events in patients with non-Hodgkin lymphoma treated with first-line cyclophosphamide, doxorubicin, vincristine, and prednisone (CHOP) or CHOP with rituximab (R-CHOP): a systematic review and meta-analysis. Lancet Haematol. 2020;7(4):e295–308.CrossRef
41.
go back to reference Lazzerini PE, et al. Biologic drugs and arrhythmic risk in chronic inflammatory arthritis: the good and the bad. Immunol Res. 2017;65(1):262–75.CrossRef Lazzerini PE, et al. Biologic drugs and arrhythmic risk in chronic inflammatory arthritis: the good and the bad. Immunol Res. 2017;65(1):262–75.CrossRef
42.
go back to reference Kilickap S, et al. Addition of rituximab to chop does not increase the risk of cardiotoxicity in patients with non-Hodgkin’s lymphoma. Med Oncol. 2008;25(4):437–42.CrossRef Kilickap S, et al. Addition of rituximab to chop does not increase the risk of cardiotoxicity in patients with non-Hodgkin’s lymphoma. Med Oncol. 2008;25(4):437–42.CrossRef
43.
go back to reference Chen DM, et al. Rituximab is an effective treatment in patients with pemphigus vulgaris and demonstrates a steroid-sparing effect. Br J Dermatol. 2020;182(5):1111–9.CrossRef Chen DM, et al. Rituximab is an effective treatment in patients with pemphigus vulgaris and demonstrates a steroid-sparing effect. Br J Dermatol. 2020;182(5):1111–9.CrossRef
44.
go back to reference Werth VP, et al. Rituximab versus mycophenolate mofetil in patients with pemphigus vulgaris. N Engl J Med. 2021;384(24):2295–305.CrossRef Werth VP, et al. Rituximab versus mycophenolate mofetil in patients with pemphigus vulgaris. N Engl J Med. 2021;384(24):2295–305.CrossRef
45.
go back to reference Agarwal A, et al. Comparison of rituximab and conventional adjuvant therapy for pemphigus vulgaris: a retrospective analysis. PLoS ONE. 2018;13(9):e0198074.CrossRef Agarwal A, et al. Comparison of rituximab and conventional adjuvant therapy for pemphigus vulgaris: a retrospective analysis. PLoS ONE. 2018;13(9):e0198074.CrossRef
46.
go back to reference MacIsaac J, et al. Systematic review of rituximab for autoimmune diseases: a potential alternative to intravenous immune globulin. Transfusion. 2018;58(11):2729–35.CrossRef MacIsaac J, et al. Systematic review of rituximab for autoimmune diseases: a potential alternative to intravenous immune globulin. Transfusion. 2018;58(11):2729–35.CrossRef
47.
go back to reference Emery P, et al. The efficacy and safety of rituximab in patients with active rheumatoid arthritis despite methotrexate treatment: results of a phase IIB randomized, double-blind, placebo-controlled, dose-ranging trial. Arthritis Rheum. 2006;54(5):1390–400.CrossRef Emery P, et al. The efficacy and safety of rituximab in patients with active rheumatoid arthritis despite methotrexate treatment: results of a phase IIB randomized, double-blind, placebo-controlled, dose-ranging trial. Arthritis Rheum. 2006;54(5):1390–400.CrossRef
48.
go back to reference McLaughlin P, et al. Rituximab chimeric anti-CD20 monoclonal antibody therapy for relapsed indolent lymphoma: half of patients respond to a four-dose treatment program. J Clin Oncol. 1998;16(8):2825–33.CrossRef McLaughlin P, et al. Rituximab chimeric anti-CD20 monoclonal antibody therapy for relapsed indolent lymphoma: half of patients respond to a four-dose treatment program. J Clin Oncol. 1998;16(8):2825–33.CrossRef
49.
go back to reference Looney RJ, et al. B cell depletion as a novel treatment for systemic lupus erythematosus: a phase I/II dose-escalation trial of rituximab. Arthritis Rheum. 2004;50(8):2580–9.CrossRef Looney RJ, et al. B cell depletion as a novel treatment for systemic lupus erythematosus: a phase I/II dose-escalation trial of rituximab. Arthritis Rheum. 2004;50(8):2580–9.CrossRef
50.
go back to reference Carson KR, et al. Progressive multifocal leukoencephalopathy after rituximab therapy in HIV-negative patients: a report of 57 cases from the research on adverse drug events and reports project. Blood. 2009;113(20):4834–40.CrossRef Carson KR, et al. Progressive multifocal leukoencephalopathy after rituximab therapy in HIV-negative patients: a report of 57 cases from the research on adverse drug events and reports project. Blood. 2009;113(20):4834–40.CrossRef
51.
go back to reference Amber KT, et al. The controversy of hepatitis C and rituximab: a multidisciplinary dilemma with implications for patients with pemphigus. Indian J Dermatol Venereol Leprol. 2016;82(2):182–3.CrossRef Amber KT, et al. The controversy of hepatitis C and rituximab: a multidisciplinary dilemma with implications for patients with pemphigus. Indian J Dermatol Venereol Leprol. 2016;82(2):182–3.CrossRef
52.
go back to reference Quartuccio L, et al. Retreatment regimen of rituximab monotherapy given at the relapse of severe HCV-related cryoglobulinemic vasculitis: long-term follow up data of a randomized controlled multicentre study. J Autoimmun. 2015;63:88–93.CrossRef Quartuccio L, et al. Retreatment regimen of rituximab monotherapy given at the relapse of severe HCV-related cryoglobulinemic vasculitis: long-term follow up data of a randomized controlled multicentre study. J Autoimmun. 2015;63:88–93.CrossRef
53.
go back to reference Buch MH, et al. Updated consensus statement on the use of rituximab in patients with rheumatoid arthritis. Ann Rheum Dis. 2011;70(6):909–20.CrossRef Buch MH, et al. Updated consensus statement on the use of rituximab in patients with rheumatoid arthritis. Ann Rheum Dis. 2011;70(6):909–20.CrossRef
54.
go back to reference Colquhoun M, et al. Rituximab administration during the 2nd trimester of pregnancy for systemic lupus erythematosus: case report and review of the literature in rheumatic disease. Mod Rheumatol Case Rep. 2021;6(2):173–7.CrossRef Colquhoun M, et al. Rituximab administration during the 2nd trimester of pregnancy for systemic lupus erythematosus: case report and review of the literature in rheumatic disease. Mod Rheumatol Case Rep. 2021;6(2):173–7.CrossRef
55.
go back to reference Seyed Ahadi M, et al. Pregnancy outcome in patients with neuromyelitis optica spectrum disorder treated with rituximab: a case-series study. Caspian J Intern Med. 2021;12(Suppl 2):S491–4. Seyed Ahadi M, et al. Pregnancy outcome in patients with neuromyelitis optica spectrum disorder treated with rituximab: a case-series study. Caspian J Intern Med. 2021;12(Suppl 2):S491–4.
56.
go back to reference Evens AM, et al. Rituximab-associated hepatitis B virus (HBV) reactivation in lymphoproliferative diseases: meta-analysis and examination of FDA safety reports. Ann Oncol. 2011;22(5):1170–80.CrossRef Evens AM, et al. Rituximab-associated hepatitis B virus (HBV) reactivation in lymphoproliferative diseases: meta-analysis and examination of FDA safety reports. Ann Oncol. 2011;22(5):1170–80.CrossRef
57.
go back to reference Mozessohn L, et al. Hepatitis B reactivation in HBsAg-negative/HBcAb-positive patients receiving rituximab for lymphoma: a meta-analysis. J Viral Hepat. 2015;22(10):842–9.CrossRef Mozessohn L, et al. Hepatitis B reactivation in HBsAg-negative/HBcAb-positive patients receiving rituximab for lymphoma: a meta-analysis. J Viral Hepat. 2015;22(10):842–9.CrossRef
58.
go back to reference Pei SN, et al. Analysis of hepatitis B surface antibody titers in B cell lymphoma patients after rituximab therapy. Ann Hematol. 2012;91(7):1007–12.CrossRef Pei SN, et al. Analysis of hepatitis B surface antibody titers in B cell lymphoma patients after rituximab therapy. Ann Hematol. 2012;91(7):1007–12.CrossRef
59.
go back to reference Loomba R, Liang TJ. Hepatitis B reactivation associated with immune suppressive and biological modifier therapies: current concepts, management strategies, and future directions. Gastroenterology. 2017;152(6):1297–309.CrossRef Loomba R, Liang TJ. Hepatitis B reactivation associated with immune suppressive and biological modifier therapies: current concepts, management strategies, and future directions. Gastroenterology. 2017;152(6):1297–309.CrossRef
60.
go back to reference Ceccarelli L, et al. Late hepatitis B virus reactivation after lamivudine prophylaxis interruption in an anti-HBs-positive and anti-HBc-negative patient treated with rituximab-containing therapy. J Infect. 2012;65(2):180–3.CrossRef Ceccarelli L, et al. Late hepatitis B virus reactivation after lamivudine prophylaxis interruption in an anti-HBs-positive and anti-HBc-negative patient treated with rituximab-containing therapy. J Infect. 2012;65(2):180–3.CrossRef
61.
go back to reference Myers RP, et al. Reactivation of hepatitis B e antigen-negative chronic hepatitis B in a bone marrow transplant recipient following lamivudine withdrawal. Can J Gastroenterol. 2001;15(9):599–603.CrossRef Myers RP, et al. Reactivation of hepatitis B e antigen-negative chronic hepatitis B in a bone marrow transplant recipient following lamivudine withdrawal. Can J Gastroenterol. 2001;15(9):599–603.CrossRef
62.
go back to reference Sagnelli E, et al. Rituximab-based treatment, HCV replication, and hepatic flares. Clin Dev Immunol. 2012;2012:945950.CrossRef Sagnelli E, et al. Rituximab-based treatment, HCV replication, and hepatic flares. Clin Dev Immunol. 2012;2012:945950.CrossRef
63.
go back to reference Ennishi D, et al. Does rituximab really induce hepatitis C virus reactivation? J Clin Oncol. 2008;26(28):4695–6 author reply 4696.CrossRef Ennishi D, et al. Does rituximab really induce hepatitis C virus reactivation? J Clin Oncol. 2008;26(28):4695–6 author reply 4696.CrossRef
64.
go back to reference Saag KG, et al. American College of Rheumatology 2008 recommendations for the use of nonbiologic and biologic disease-modifying antirheumatic drugs in rheumatoid arthritis. Arthritis Rheum. 2008;59(6):762–84.CrossRef Saag KG, et al. American College of Rheumatology 2008 recommendations for the use of nonbiologic and biologic disease-modifying antirheumatic drugs in rheumatoid arthritis. Arthritis Rheum. 2008;59(6):762–84.CrossRef
65.
go back to reference Alkadi A, Alduaiji N, Alrehaily A. Risk of tuberculosis reactivation with rituximab therapy. Int J Health Sci. 2017;11(2):41–4. Alkadi A, Alduaiji N, Alrehaily A. Risk of tuberculosis reactivation with rituximab therapy. Int J Health Sci. 2017;11(2):41–4.
66.
go back to reference Ottaviani S, et al. Knee tuberculosis under rituximab therapy for rheumatoid arthritis. Joint Bone Spine. 2013;80(4):435–6.CrossRef Ottaviani S, et al. Knee tuberculosis under rituximab therapy for rheumatoid arthritis. Joint Bone Spine. 2013;80(4):435–6.CrossRef
67.
go back to reference Amber KT, et al. Targeted therapies for autoimmune bullous diseases: current status. Drugs. 2018;78(15):1527–48.CrossRef Amber KT, et al. Targeted therapies for autoimmune bullous diseases: current status. Drugs. 2018;78(15):1527–48.CrossRef
68.
go back to reference Gottenberg JE, et al. Risk factors for severe infections in patients with rheumatoid arthritis treated with rituximab in the autoimmunity and rituximab registry. Arthritis Rheum. 2010;62(9):2625–32.CrossRef Gottenberg JE, et al. Risk factors for severe infections in patients with rheumatoid arthritis treated with rituximab in the autoimmunity and rituximab registry. Arthritis Rheum. 2010;62(9):2625–32.CrossRef
69.
go back to reference Strangfeld A, et al. Factors associated with COVID-19-related death in people with rheumatic diseases: results from the COVID-19 global rheumatology alliance physician-reported registry. Ann Rheum Dis. 2021;80(7):930–42.CrossRef Strangfeld A, et al. Factors associated with COVID-19-related death in people with rheumatic diseases: results from the COVID-19 global rheumatology alliance physician-reported registry. Ann Rheum Dis. 2021;80(7):930–42.CrossRef
70.
go back to reference Mahmoudi H, et al. Characteristics and outcomes of COVID-19 in patients with autoimmune bullous diseases: a retrospective cohort study. J Am Acad Dermatol. 2021;84(4):1098–100.CrossRef Mahmoudi H, et al. Characteristics and outcomes of COVID-19 in patients with autoimmune bullous diseases: a retrospective cohort study. J Am Acad Dermatol. 2021;84(4):1098–100.CrossRef
71.
go back to reference Joly P, French study Group on auto immune bullous skin diseases, and the French network of rare diseases in Dermatology (FIMARAD). Incidence and severity of COVID-19 in patients with autoimmune blistering skin diseases: A nationwide study. J Am Acad Dermatol. 2022;86(2):494–7.CrossRef Joly P, French study Group on auto immune bullous skin diseases, and the French network of rare diseases in Dermatology (FIMARAD). Incidence and severity of COVID-19 in patients with autoimmune blistering skin diseases: A nationwide study. J Am Acad Dermatol. 2022;86(2):494–7.CrossRef
72.
go back to reference Levavi H, Lancman G, Gabrilove J. Impact of rituximab on COVID-19 outcomes. Ann Hematol. 2021;100(11):2805–12.CrossRef Levavi H, Lancman G, Gabrilove J. Impact of rituximab on COVID-19 outcomes. Ann Hematol. 2021;100(11):2805–12.CrossRef
73.
go back to reference Eming R, et al. Rituximab exerts a dual effect in pemphigus vulgaris. J Invest Dermatol. 2008;128(12):2850–8.CrossRef Eming R, et al. Rituximab exerts a dual effect in pemphigus vulgaris. J Invest Dermatol. 2008;128(12):2850–8.CrossRef
74.
go back to reference Herrmann G, Hunzelmann N, Engert A. Treatment of pemphigus vulgaris with anti-CD20 monoclonal antibody (rituximab). Br J Dermatol. 2003;148(3):602–3.CrossRef Herrmann G, Hunzelmann N, Engert A. Treatment of pemphigus vulgaris with anti-CD20 monoclonal antibody (rituximab). Br J Dermatol. 2003;148(3):602–3.CrossRef
75.
go back to reference Morrison LH. Therapy of refractory pemphigus vulgaris with monoclonal anti-CD20 antibody (rituximab). J Am Acad Dermatol. 2004;51(5):817–9.CrossRef Morrison LH. Therapy of refractory pemphigus vulgaris with monoclonal anti-CD20 antibody (rituximab). J Am Acad Dermatol. 2004;51(5):817–9.CrossRef
76.
go back to reference Murrell DF, Sprecher E. Rituximab and short-course prednisone as the new gold standard for new-onset pemphigus vulgaris and pemphigus foliaceus. Br J Dermatol. 2017;177(5):1143–4.CrossRef Murrell DF, Sprecher E. Rituximab and short-course prednisone as the new gold standard for new-onset pemphigus vulgaris and pemphigus foliaceus. Br J Dermatol. 2017;177(5):1143–4.CrossRef
77.
go back to reference Vinay K, et al. Rituximab as first-line adjuvant therapy for pemphigus: retrospective analysis of long-term outcomes at a single center. J Am Acad Dermatol. 2018;78(4):806–8.CrossRef Vinay K, et al. Rituximab as first-line adjuvant therapy for pemphigus: retrospective analysis of long-term outcomes at a single center. J Am Acad Dermatol. 2018;78(4):806–8.CrossRef
78.
go back to reference Fuertes I, et al. Rituximab in childhood pemphigus vulgaris: a long-term follow-up case and review of the literature. Dermatology. 2010;221(1):13–6.CrossRef Fuertes I, et al. Rituximab in childhood pemphigus vulgaris: a long-term follow-up case and review of the literature. Dermatology. 2010;221(1):13–6.CrossRef
79.
go back to reference Borradori L, et al. Anti-CD20 monoclonal antibody (rituximab) for refractory erosive stomatitis secondary to CD20(+) follicular lymphoma-associated paraneoplastic pemphigus. Arch Dermatol. 2001;137(3):269–72. Borradori L, et al. Anti-CD20 monoclonal antibody (rituximab) for refractory erosive stomatitis secondary to CD20(+) follicular lymphoma-associated paraneoplastic pemphigus. Arch Dermatol. 2001;137(3):269–72.
80.
go back to reference Heizmann M, et al. Successful treatment of paraneoplastic pemphigus in follicular NHL with rituximab: report of a case and review of treatment for paraneoplastic pemphigus in NHL and CLL. Am J Hematol. 2001;66(2):142–4.CrossRef Heizmann M, et al. Successful treatment of paraneoplastic pemphigus in follicular NHL with rituximab: report of a case and review of treatment for paraneoplastic pemphigus in NHL and CLL. Am J Hematol. 2001;66(2):142–4.CrossRef
81.
go back to reference Fatourechi MM, El-Azhary RA, Gibson LE. Rituximab: applications in dermatology. Int J Dermatol. 2006;45(10):1143–55.CrossRef Fatourechi MM, El-Azhary RA, Gibson LE. Rituximab: applications in dermatology. Int J Dermatol. 2006;45(10):1143–55.CrossRef
82.
go back to reference Goebeler M, et al. Rapid response of treatment-resistant pemphigus foliaceus to the anti-CD20 antibody rituximab. Br J Dermatol. 2003;149(4):899–901.CrossRef Goebeler M, et al. Rapid response of treatment-resistant pemphigus foliaceus to the anti-CD20 antibody rituximab. Br J Dermatol. 2003;149(4):899–901.CrossRef
83.
go back to reference Amber KT, Valdebran M, Grando SA. Paraneoplastic autoimmune multiorgan syndrome (PAMS): beyond the single phenotype of paraneoplastic pemphigus. Autoimmun Rev. 2018;17(10):1002–10.CrossRef Amber KT, Valdebran M, Grando SA. Paraneoplastic autoimmune multiorgan syndrome (PAMS): beyond the single phenotype of paraneoplastic pemphigus. Autoimmun Rev. 2018;17(10):1002–10.CrossRef
84.
go back to reference Feliciani C, et al. Management of bullous pemphigoid: the European Dermatology Forum consensus in collaboration with the European Academy of Dermatology and Venereology. Br J Dermatol. 2015;172(4):867–77.CrossRef Feliciani C, et al. Management of bullous pemphigoid: the European Dermatology Forum consensus in collaboration with the European Academy of Dermatology and Venereology. Br J Dermatol. 2015;172(4):867–77.CrossRef
85.
go back to reference Tovanabutra N, Payne AS. Clinical outcome and safety of rituximab therapy for pemphigoid diseases. J Am Acad Dermatol. 2020;82(5):1237–9.CrossRef Tovanabutra N, Payne AS. Clinical outcome and safety of rituximab therapy for pemphigoid diseases. J Am Acad Dermatol. 2020;82(5):1237–9.CrossRef
86.
go back to reference Ahmed AR, et al. Treatment of recalcitrant bullous pemphigoid (BP) with a novel protocol: a retrospective study with a 6-year follow-up. J Am Acad Dermatol. 2016;74(4):700–8.CrossRef Ahmed AR, et al. Treatment of recalcitrant bullous pemphigoid (BP) with a novel protocol: a retrospective study with a 6-year follow-up. J Am Acad Dermatol. 2016;74(4):700–8.CrossRef
87.
go back to reference Cho YT, Chu CY, Wang LF. First-line combination therapy with rituximab and corticosteroids provides a high complete remission rate in moderate-to-severe bullous pemphigoid. Br J Dermatol. 2015;173(1):302–4.CrossRef Cho YT, Chu CY, Wang LF. First-line combination therapy with rituximab and corticosteroids provides a high complete remission rate in moderate-to-severe bullous pemphigoid. Br J Dermatol. 2015;173(1):302–4.CrossRef
88.
go back to reference Polansky M, et al. Rituximab therapy in patients with bullous pemphigoid: a retrospective study of 20 patients. J Am Acad Dermatol. 2019;81(1):179–86.CrossRef Polansky M, et al. Rituximab therapy in patients with bullous pemphigoid: a retrospective study of 20 patients. J Am Acad Dermatol. 2019;81(1):179–86.CrossRef
89.
go back to reference Kolesnik M, et al. Treatment of severe autoimmune blistering skin diseases with combination of protein A immunoadsorption and rituximab: a protocol without initial high dose or pulse steroid medication. J Eur Acad Dermatol Venereol. 2014;28(6):771–80.CrossRef Kolesnik M, et al. Treatment of severe autoimmune blistering skin diseases with combination of protein A immunoadsorption and rituximab: a protocol without initial high dose or pulse steroid medication. J Eur Acad Dermatol Venereol. 2014;28(6):771–80.CrossRef
90.
go back to reference Lourari S, et al. Bullous and mucous membrane pemphigoid show a mixed response to rituximab: experience in seven patients. J Eur Acad Dermatol Venereol. 2011;25(10):1238–40.CrossRef Lourari S, et al. Bullous and mucous membrane pemphigoid show a mixed response to rituximab: experience in seven patients. J Eur Acad Dermatol Venereol. 2011;25(10):1238–40.CrossRef
91.
go back to reference Kasperkiewicz M, et al. Rituximab for treatment-refractory pemphigus and pemphigoid: a case series of 17 patients. J Am Acad Dermatol. 2011;65(3):552–8.CrossRef Kasperkiewicz M, et al. Rituximab for treatment-refractory pemphigus and pemphigoid: a case series of 17 patients. J Am Acad Dermatol. 2011;65(3):552–8.CrossRef
92.
go back to reference Bilgic Temel A, et al. Successful treatment of a bullous pemphigoid patient with rituximab who was refractory to corticosteroid and omalizumab treatments. Case Rep Dermatol. 2017;9(1):38–44.CrossRef Bilgic Temel A, et al. Successful treatment of a bullous pemphigoid patient with rituximab who was refractory to corticosteroid and omalizumab treatments. Case Rep Dermatol. 2017;9(1):38–44.CrossRef
93.
go back to reference Tomsitz D, Stefaniak R, Worm M. Rituximab in patients with recalcitrant autoimmune blistering diseases: experience in a cohort of 22 patients. Br J Dermatol. 2015;172(3):829–31.CrossRef Tomsitz D, Stefaniak R, Worm M. Rituximab in patients with recalcitrant autoimmune blistering diseases: experience in a cohort of 22 patients. Br J Dermatol. 2015;172(3):829–31.CrossRef
94.
go back to reference Batts AF, et al. Exacerbation of bullous pemphigoid after hand, foot, and mouth disease treated with rituximab. JAAD Case Rep. 2016;2(1):7–9.CrossRef Batts AF, et al. Exacerbation of bullous pemphigoid after hand, foot, and mouth disease treated with rituximab. JAAD Case Rep. 2016;2(1):7–9.CrossRef
95.
go back to reference Tourte M, et al. Pemphigoid gestationis: a successful preventive treatment by rituximab. J Eur Acad Dermatol Venereol. 2017;31(4):e206–7.CrossRef Tourte M, et al. Pemphigoid gestationis: a successful preventive treatment by rituximab. J Eur Acad Dermatol Venereol. 2017;31(4):e206–7.CrossRef
96.
go back to reference Cianchini G, et al. Severe persistent pemphigoid gestationis: long-term remission with rituximab. Br J Dermatol. 2007;157(2):388–9.CrossRef Cianchini G, et al. Severe persistent pemphigoid gestationis: long-term remission with rituximab. Br J Dermatol. 2007;157(2):388–9.CrossRef
97.
go back to reference Ridpath AV, et al. Novel use of combination therapeutic plasma exchange and rituximab in the treatment of nivolumab-induced bullous pemphigoid. Int J Dermatol. 2018;57(11):1372–4.CrossRef Ridpath AV, et al. Novel use of combination therapeutic plasma exchange and rituximab in the treatment of nivolumab-induced bullous pemphigoid. Int J Dermatol. 2018;57(11):1372–4.CrossRef
98.
go back to reference Sowerby L, et al. Rituximab treatment of nivolumab-induced bullous pemphigoid. JAMA Dermatol. 2017;153(6):603–5.CrossRef Sowerby L, et al. Rituximab treatment of nivolumab-induced bullous pemphigoid. JAMA Dermatol. 2017;153(6):603–5.CrossRef
99.
go back to reference Kremer N, et al. Rituximab and omalizumab for the treatment of bullous pemphigoid: a systematic review of the literature. Am J Clin Dermatol. 2019;20(2):209–16.CrossRef Kremer N, et al. Rituximab and omalizumab for the treatment of bullous pemphigoid: a systematic review of the literature. Am J Clin Dermatol. 2019;20(2):209–16.CrossRef
100.
go back to reference Lamberts A, et al. Effectiveness and safety of rituximab in recalcitrant pemphigoid diseases. Front Immunol. 2018;9:248.CrossRef Lamberts A, et al. Effectiveness and safety of rituximab in recalcitrant pemphigoid diseases. Front Immunol. 2018;9:248.CrossRef
101.
go back to reference Schmidt E, et al. Rituximab in autoimmune bullous diseases: mixed responses and adverse effects. Br J Dermatol. 2007;156(2):352–6.CrossRef Schmidt E, et al. Rituximab in autoimmune bullous diseases: mixed responses and adverse effects. Br J Dermatol. 2007;156(2):352–6.CrossRef
102.
go back to reference Thomas RM, Colon A, Motaparthi K. Rituximab in autoimmune pemphigoid diseases: indications, optimized regimens, and practice gaps. Clin Dermatol. 2020;38(3):384–96.CrossRef Thomas RM, Colon A, Motaparthi K. Rituximab in autoimmune pemphigoid diseases: indications, optimized regimens, and practice gaps. Clin Dermatol. 2020;38(3):384–96.CrossRef
103.
go back to reference Murrell DF, et al. Definitions and outcome measures for mucous membrane pemphigoid: recommendations of an international panel of experts. J Am Acad Dermatol. 2015;72(1):168–74.CrossRef Murrell DF, et al. Definitions and outcome measures for mucous membrane pemphigoid: recommendations of an international panel of experts. J Am Acad Dermatol. 2015;72(1):168–74.CrossRef
104.
go back to reference Li Y, Foshee JB, Sontheimer RD. Sustained clinical response to rituximab in a case of life-threatening overlap subepidermal autoimmune blistering disease. J Am Acad Dermatol. 2011;64(4):773–8.CrossRef Li Y, Foshee JB, Sontheimer RD. Sustained clinical response to rituximab in a case of life-threatening overlap subepidermal autoimmune blistering disease. J Am Acad Dermatol. 2011;64(4):773–8.CrossRef
105.
go back to reference Maley A, et al. Rituximab combined with conventional therapy versus conventional therapy alone for the treatment of mucous membrane pemphigoid (MMP). J Am Acad Dermatol. 2016;74(5):835–40.CrossRef Maley A, et al. Rituximab combined with conventional therapy versus conventional therapy alone for the treatment of mucous membrane pemphigoid (MMP). J Am Acad Dermatol. 2016;74(5):835–40.CrossRef
106.
go back to reference Nishimura R, et al. Refractory mucous membrane pemphigoid which developed after allogeneic stem cell transplantation and was successfully treated with rituximab. Eur J Dermatol. 2013;23(4):562–4.CrossRef Nishimura R, et al. Refractory mucous membrane pemphigoid which developed after allogeneic stem cell transplantation and was successfully treated with rituximab. Eur J Dermatol. 2013;23(4):562–4.CrossRef
107.
go back to reference Schumann T, et al. Successful treatment of mucous membrane pemphigoid with the anti-CD-20 antibody rituximab. Acta Derm Venereol. 2009;89(1):101–2.CrossRef Schumann T, et al. Successful treatment of mucous membrane pemphigoid with the anti-CD-20 antibody rituximab. Acta Derm Venereol. 2009;89(1):101–2.CrossRef
108.
go back to reference Taverna JA, et al. Successful adjuvant treatment of recalcitrant mucous membrane pemphigoid with anti-CD20 antibody rituximab. J Drugs Dermatol. 2007;6(7):731–2. Taverna JA, et al. Successful adjuvant treatment of recalcitrant mucous membrane pemphigoid with anti-CD20 antibody rituximab. J Drugs Dermatol. 2007;6(7):731–2.
109.
go back to reference Amir Dastmalchi D, et al. The efficacy of rituximab in patients with mucous membrane pemphigoid. J Dermatolog Treat. 2022;33(2):1084–90.CrossRef Amir Dastmalchi D, et al. The efficacy of rituximab in patients with mucous membrane pemphigoid. J Dermatolog Treat. 2022;33(2):1084–90.CrossRef
110.
go back to reference Le Roux-Villet C, et al. Rituximab for patients with refractory mucous membrane pemphigoid. Arch Dermatol. 2011;147(7):843–9.CrossRef Le Roux-Villet C, et al. Rituximab for patients with refractory mucous membrane pemphigoid. Arch Dermatol. 2011;147(7):843–9.CrossRef
111.
go back to reference Lytvyn Y, et al. Biologic treatment outcomes in mucous membrane pemphigoid: a systematic review. J Am Acad Dermatol. 2021;87(1):110–20.CrossRef Lytvyn Y, et al. Biologic treatment outcomes in mucous membrane pemphigoid: a systematic review. J Am Acad Dermatol. 2021;87(1):110–20.CrossRef
112.
go back to reference Haefliger S, et al. Rituximab for the treatment of isolated refractory desquamative gingivitis due to mucous membrane pemphigoid. JAMA Dermatol. 2016;152(12):1396–8.CrossRef Haefliger S, et al. Rituximab for the treatment of isolated refractory desquamative gingivitis due to mucous membrane pemphigoid. JAMA Dermatol. 2016;152(12):1396–8.CrossRef
113.
go back to reference Foster CS, Chang PY, Ahmed AR. Combination of rituximab and intravenous immunoglobulin for recalcitrant ocular cicatricial pemphigoid: a preliminary report. Ophthalmology. 2010;117(5):861–9.CrossRef Foster CS, Chang PY, Ahmed AR. Combination of rituximab and intravenous immunoglobulin for recalcitrant ocular cicatricial pemphigoid: a preliminary report. Ophthalmology. 2010;117(5):861–9.CrossRef
114.
go back to reference Rubsam A, et al. Rituximab preserves vision in ocular mucous membrane pemphigoid. Expert Opin Biol Ther. 2015;15(7):927–33.CrossRef Rubsam A, et al. Rituximab preserves vision in ocular mucous membrane pemphigoid. Expert Opin Biol Ther. 2015;15(7):927–33.CrossRef
115.
go back to reference Steger B, et al. Combined use of rituximab and intravenous immunoglobulin for severe autoimmune cicatricial conjunctivitis-an interventional case series. Cornea. 2016;35(12):1611–4.CrossRef Steger B, et al. Combined use of rituximab and intravenous immunoglobulin for severe autoimmune cicatricial conjunctivitis-an interventional case series. Cornea. 2016;35(12):1611–4.CrossRef
116.
go back to reference Tazudeen N, et al. IgM ocular cicatricial pemphigoid: a unique insight into the immune system. Dermatol Online J. 2015;21(10). Tazudeen N, et al. IgM ocular cicatricial pemphigoid: a unique insight into the immune system. Dermatol Online J. 2015;21(10).
117.
go back to reference Wollina U, et al. Monoclonal anti-CD20 antibody therapy in cicatrical pemphigoid with oral and hypopharyngeal involvement and related conditions. J Clin Aesthet Dermatol. 2013;6(5):45–8. Wollina U, et al. Monoclonal anti-CD20 antibody therapy in cicatrical pemphigoid with oral and hypopharyngeal involvement and related conditions. J Clin Aesthet Dermatol. 2013;6(5):45–8.
118.
go back to reference Lambiel S, et al. Paraneoplastic mucous membrane pemphigoid with ocular and laryngeal involvement. BMJ Case Rep. 2017. Lambiel S, et al. Paraneoplastic mucous membrane pemphigoid with ocular and laryngeal involvement. BMJ Case Rep. 2017.
119.
go back to reference Wilder E, Fernandez MP, Krejci-Manwaring J. Mucous membrane pemphigoid involving the trachea and bronchi: an extremely rare and life-threatening presentation. Cutis. 2016;98(3):E24–7. Wilder E, Fernandez MP, Krejci-Manwaring J. Mucous membrane pemphigoid involving the trachea and bronchi: an extremely rare and life-threatening presentation. Cutis. 2016;98(3):E24–7.
120.
go back to reference Kim JH, Lee SE, Kim SC. Successful treatment of epidermolysis bullosa acquisita with rituximab therapy. J Dermatol. 2012;39(5):477–9.CrossRef Kim JH, Lee SE, Kim SC. Successful treatment of epidermolysis bullosa acquisita with rituximab therapy. J Dermatol. 2012;39(5):477–9.CrossRef
121.
go back to reference Oktem A, et al. Long-term results of rituximab-intravenous immunoglobulin combination therapy in patients with epidermolysis bullosa acquisita resistant to conventional therapy. J Dermatolog Treat. 2017;28(1):50–4.CrossRef Oktem A, et al. Long-term results of rituximab-intravenous immunoglobulin combination therapy in patients with epidermolysis bullosa acquisita resistant to conventional therapy. J Dermatolog Treat. 2017;28(1):50–4.CrossRef
122.
go back to reference Crichlow SM, Mortimer NJ, Harman KE. A successful therapeutic trial of rituximab in the treatment of a patient with recalcitrant, high-titre epidermolysis bullosa acquisita. Br J Dermatol. 2007;156(1):194–6.CrossRef Crichlow SM, Mortimer NJ, Harman KE. A successful therapeutic trial of rituximab in the treatment of a patient with recalcitrant, high-titre epidermolysis bullosa acquisita. Br J Dermatol. 2007;156(1):194–6.CrossRef
123.
go back to reference McKinley SK, et al. A case of recalcitrant epidermolysis bullosa acquisita responsive to rituximab therapy. Pediatr Dermatol. 2014;31(2):241–4.CrossRef McKinley SK, et al. A case of recalcitrant epidermolysis bullosa acquisita responsive to rituximab therapy. Pediatr Dermatol. 2014;31(2):241–4.CrossRef
124.
go back to reference Niedermeier A, et al. Clinical response of severe mechanobullous epidermolysis bullosa acquisita to combined treatment with immunoadsorption and rituximab (anti-CD20 monoclonal antibodies). Arch Dermatol. 2007;143(2):192–8.CrossRef Niedermeier A, et al. Clinical response of severe mechanobullous epidermolysis bullosa acquisita to combined treatment with immunoadsorption and rituximab (anti-CD20 monoclonal antibodies). Arch Dermatol. 2007;143(2):192–8.CrossRef
125.
go back to reference Sadler E, et al. Treatment-resistant classical epidermolysis bullosa acquisita responding to rituximab. Br J Dermatol. 2007;157(2):417–9.CrossRef Sadler E, et al. Treatment-resistant classical epidermolysis bullosa acquisita responding to rituximab. Br J Dermatol. 2007;157(2):417–9.CrossRef
126.
go back to reference Saha M, et al. Refractory epidermolysis bullosa acquisita: successful treatment with rituximab. Clin Exp Dermatol. 2009;34(8):e979–80.CrossRef Saha M, et al. Refractory epidermolysis bullosa acquisita: successful treatment with rituximab. Clin Exp Dermatol. 2009;34(8):e979–80.CrossRef
127.
go back to reference Schmidt E, et al. Successful adjuvant treatment of recalcitrant epidermolysis bullosa acquisita with anti-CD20 antibody rituximab. Arch Dermatol. 2006;142(2):147–50.CrossRef Schmidt E, et al. Successful adjuvant treatment of recalcitrant epidermolysis bullosa acquisita with anti-CD20 antibody rituximab. Arch Dermatol. 2006;142(2):147–50.CrossRef
128.
go back to reference Bevans SL, Sami N. The use of rituximab in treatment of epidermolysis bullosa acquisita: Three new cases and a review of the literature. Dermatol Ther. 2018;31(6):e12726.CrossRef Bevans SL, Sami N. The use of rituximab in treatment of epidermolysis bullosa acquisita: Three new cases and a review of the literature. Dermatol Ther. 2018;31(6):e12726.CrossRef
129.
go back to reference Cavailhes A, et al. Successful use of combined corticosteroids and rituximab in the treatment of recalcitrant epidermolysis bullosa acquisita. Ann Dermatol Venereol. 2009;136(11):795–9.CrossRef Cavailhes A, et al. Successful use of combined corticosteroids and rituximab in the treatment of recalcitrant epidermolysis bullosa acquisita. Ann Dermatol Venereol. 2009;136(11):795–9.CrossRef
130.
go back to reference Mendes SR, Coutinho I, Cardoso JC. Epidermolysis bullosa acquisita treated with rituximab. BMJ Case Rep. 2021;14(7):e243432.CrossRef Mendes SR, Coutinho I, Cardoso JC. Epidermolysis bullosa acquisita treated with rituximab. BMJ Case Rep. 2021;14(7):e243432.CrossRef
131.
go back to reference Iwata H, et al. Meta-analysis of the clinical and immunopathological characteristics and treatment outcomes in epidermolysis bullosa acquisita patients. Orphanet J Rare Dis. 2018;13(1):153.CrossRef Iwata H, et al. Meta-analysis of the clinical and immunopathological characteristics and treatment outcomes in epidermolysis bullosa acquisita patients. Orphanet J Rare Dis. 2018;13(1):153.CrossRef
132.
go back to reference Kubisch I, et al. Premonitory epidermolysis bullosa acquisita mimicking eyelid dermatitis: successful treatment with rituximab and protein A immunoapheresis. Am J Clin Dermatol. 2010;11(4):289–93. Kubisch I, et al. Premonitory epidermolysis bullosa acquisita mimicking eyelid dermatitis: successful treatment with rituximab and protein A immunoapheresis. Am J Clin Dermatol. 2010;11(4):289–93.
133.
go back to reference Koga H, et al. Epidermolysis bullosa acquisita: the 2019 update. Front Med. 2018;5:362.CrossRef Koga H, et al. Epidermolysis bullosa acquisita: the 2019 update. Front Med. 2018;5:362.CrossRef
134.
go back to reference Allenbach Y, et al. Efficacy of rituximab in refractory inflammatory myopathies associated with anti- synthetase auto-antibodies: an open-label, phase II trial. PLoS ONE. 2015;10(11):e0133702.CrossRef Allenbach Y, et al. Efficacy of rituximab in refractory inflammatory myopathies associated with anti- synthetase auto-antibodies: an open-label, phase II trial. PLoS ONE. 2015;10(11):e0133702.CrossRef
135.
go back to reference Chung L, Genovese MC, Fiorentino DF. A pilot trial of rituximab in the treatment of patients with dermatomyositis. Arch Dermatol. 2007;143(6):763–7.CrossRef Chung L, Genovese MC, Fiorentino DF. A pilot trial of rituximab in the treatment of patients with dermatomyositis. Arch Dermatol. 2007;143(6):763–7.CrossRef
136.
go back to reference Bader-Meunier B, et al. Safety and efficacy of rituximab in severe juvenile dermatomyositis: results from 9 patients from the French Autoimmunity and Rituximab registry. J Rheumatol. 2011;38(7):1436–40.CrossRef Bader-Meunier B, et al. Safety and efficacy of rituximab in severe juvenile dermatomyositis: results from 9 patients from the French Autoimmunity and Rituximab registry. J Rheumatol. 2011;38(7):1436–40.CrossRef
137.
go back to reference Garcia Hernandez FJ, et al. Evaluation of the effectiveness of treatment with rituximab associated to cyclophosphamide in patients with resistant idiopathic inflammatory myopathy. Med Clin. 2010;135(6):256–9. Garcia Hernandez FJ, et al. Evaluation of the effectiveness of treatment with rituximab associated to cyclophosphamide in patients with resistant idiopathic inflammatory myopathy. Med Clin. 2010;135(6):256–9.
138.
go back to reference Mok CC, Ho LY, To CH. Rituximab for refractory polymyositis: an open-label prospective study. J Rheumatol. 2007;34(9):1864–8. Mok CC, Ho LY, To CH. Rituximab for refractory polymyositis: an open-label prospective study. J Rheumatol. 2007;34(9):1864–8.
139.
go back to reference Bauhammer J, et al. Rituximab in the treatment of Jo1 antibody-associated antisynthetase syndrome: anti-ro52 positivity as a marker for severity and treatment response. J Rheumatol. 2016;43(8):1566–74.CrossRef Bauhammer J, et al. Rituximab in the treatment of Jo1 antibody-associated antisynthetase syndrome: anti-ro52 positivity as a marker for severity and treatment response. J Rheumatol. 2016;43(8):1566–74.CrossRef
140.
go back to reference Andersson H, et al. Long-term experience with rituximab in anti-synthetase syndrome-related interstitial lung disease. Rheumatology. 2015;54(8):1420–8.CrossRef Andersson H, et al. Long-term experience with rituximab in anti-synthetase syndrome-related interstitial lung disease. Rheumatology. 2015;54(8):1420–8.CrossRef
141.
go back to reference Sem M, et al. Rituximab treatment of the anti-synthetase syndrome: a retrospective case series. Rheumatology. 2009;48(8):968–71.CrossRef Sem M, et al. Rituximab treatment of the anti-synthetase syndrome: a retrospective case series. Rheumatology. 2009;48(8):968–71.CrossRef
142.
go back to reference Sharp C, et al. Rituximab in autoimmune connective tissue disease-associated interstitial lung disease. Rheumatology. 2016;55(7):1318–24.CrossRef Sharp C, et al. Rituximab in autoimmune connective tissue disease-associated interstitial lung disease. Rheumatology. 2016;55(7):1318–24.CrossRef
143.
go back to reference Basnayake C, et al. Use of rituximab in histologically confirmed idiopathic inflammatory myositis: a case series. Clin Rheumatol. 2015;34(2):371–7.CrossRef Basnayake C, et al. Use of rituximab in histologically confirmed idiopathic inflammatory myositis: a case series. Clin Rheumatol. 2015;34(2):371–7.CrossRef
144.
go back to reference Majmudar S, Hall HA, Zimmermann B. Treatment of adult inflammatory myositis with rituximab: an emerging therapy for refractory patients. J Clin Rheumatol. 2009;15(7):338–40.CrossRef Majmudar S, Hall HA, Zimmermann B. Treatment of adult inflammatory myositis with rituximab: an emerging therapy for refractory patients. J Clin Rheumatol. 2009;15(7):338–40.CrossRef
145.
go back to reference Unger L, et al. Rituximab therapy in patients with refractory dermatomyositis or polymyositis: differential effects in a real-life population. Rheumatology. 2014;53(9):1630–8.CrossRef Unger L, et al. Rituximab therapy in patients with refractory dermatomyositis or polymyositis: differential effects in a real-life population. Rheumatology. 2014;53(9):1630–8.CrossRef
146.
go back to reference Kuye IO, Smith GP. The Use of Rituximab in the Management of Refractory Dermatomyositis. J Drugs Dermatol. 2017;16(2):162–6. Kuye IO, Smith GP. The Use of Rituximab in the Management of Refractory Dermatomyositis. J Drugs Dermatol. 2017;16(2):162–6.
147.
go back to reference Munoz-Beamud F, Isenberg DA. Rituximab as an effective alternative therapy in refractory idiopathic inflammatory myopathies. Clin Exp Rheumatol. 2013;31(6):896–903. Munoz-Beamud F, Isenberg DA. Rituximab as an effective alternative therapy in refractory idiopathic inflammatory myopathies. Clin Exp Rheumatol. 2013;31(6):896–903.
148.
go back to reference Valiyil R, et al. Rituximab therapy for myopathy associated with anti-signal recognition particle antibodies: a case series. Arthritis Care Res. 2010;62(9):1328–34.CrossRef Valiyil R, et al. Rituximab therapy for myopathy associated with anti-signal recognition particle antibodies: a case series. Arthritis Care Res. 2010;62(9):1328–34.CrossRef
149.
go back to reference Egeli BH, et al. Rituximab as a glucocorticoid-sparing agent in idiopathic inflammatory myopathies: a retrospective single-center cohort study. Clin Rheumatol. 2022;41(1):123–7.CrossRef Egeli BH, et al. Rituximab as a glucocorticoid-sparing agent in idiopathic inflammatory myopathies: a retrospective single-center cohort study. Clin Rheumatol. 2022;41(1):123–7.CrossRef
150.
go back to reference Doyle TJ, Dellaripa PF. Lung manifestations in the rheumatic diseases. Chest. 2017;152(6):1283–95.CrossRef Doyle TJ, Dellaripa PF. Lung manifestations in the rheumatic diseases. Chest. 2017;152(6):1283–95.CrossRef
151.
go back to reference Oddis CV, et al. Rituximab in the treatment of refractory adult and juvenile dermatomyositis and adult polymyositis: a randomized, placebo-phase trial. Arthritis Rheum. 2013;65(2):314–24.CrossRef Oddis CV, et al. Rituximab in the treatment of refractory adult and juvenile dermatomyositis and adult polymyositis: a randomized, placebo-phase trial. Arthritis Rheum. 2013;65(2):314–24.CrossRef
152.
go back to reference Tokunaga K, Hagino N. Dermatomyositis with rapidly progressive interstitial lung disease treated with rituximab: a report of 3 cases in Japan. Intern Med. 2017;56(11):1399–403.CrossRef Tokunaga K, Hagino N. Dermatomyositis with rapidly progressive interstitial lung disease treated with rituximab: a report of 3 cases in Japan. Intern Med. 2017;56(11):1399–403.CrossRef
153.
go back to reference Ogawa Y, et al. Effective administration of rituximab in anti-MDA5 antibody-positive dermatomyositis with rapidly progressive interstitial lung disease and refractory cutaneous involvement: a case report and literature review. Case Rep Rheumatol. 2017;2017:5386797. Ogawa Y, et al. Effective administration of rituximab in anti-MDA5 antibody-positive dermatomyositis with rapidly progressive interstitial lung disease and refractory cutaneous involvement: a case report and literature review. Case Rep Rheumatol. 2017;2017:5386797.
154.
go back to reference Levine TD. Rituximab in the treatment of dermatomyositis: an open-label pilot study. Arthritis Rheum. 2005;52(2):601–7.CrossRef Levine TD. Rituximab in the treatment of dermatomyositis: an open-label pilot study. Arthritis Rheum. 2005;52(2):601–7.CrossRef
155.
go back to reference Aggarwal R, et al. Cutaneous improvement in refractory adult and juvenile dermatomyositis after treatment with rituximab. Rheumatology. 2017;56(2):247–54.CrossRef Aggarwal R, et al. Cutaneous improvement in refractory adult and juvenile dermatomyositis after treatment with rituximab. Rheumatology. 2017;56(2):247–54.CrossRef
156.
go back to reference Dinh HV, et al. Rituximab for the treatment of the skin manifestations of dermatomyositis: a report of 3 cases. J Am Acad Dermatol. 2007;56(1):148–53.CrossRef Dinh HV, et al. Rituximab for the treatment of the skin manifestations of dermatomyositis: a report of 3 cases. J Am Acad Dermatol. 2007;56(1):148–53.CrossRef
157.
go back to reference Cobos GA, Femia A, Vleugels RA. Dermatomyositis: an update on diagnosis and treatment. Am J Clin Dermatol. 2020;21(3):339–53.CrossRef Cobos GA, Femia A, Vleugels RA. Dermatomyositis: an update on diagnosis and treatment. Am J Clin Dermatol. 2020;21(3):339–53.CrossRef
158.
go back to reference Aggarwal R, et al. Predictors of clinical improvement in rituximab-treated refractory adult and juvenile dermatomyositis and adult polymyositis. Arthritis Rheumatol. 2014;66(3):740–9.CrossRef Aggarwal R, et al. Predictors of clinical improvement in rituximab-treated refractory adult and juvenile dermatomyositis and adult polymyositis. Arthritis Rheumatol. 2014;66(3):740–9.CrossRef
159.
go back to reference Leclair V, et al. Efficacy and safety of rituximab in anti-synthetase antibody positive and negative subjects with idiopathic inflammatory myopathy: a registry-based study. Rheumatology. 2019;58(7):1214–20.CrossRef Leclair V, et al. Efficacy and safety of rituximab in anti-synthetase antibody positive and negative subjects with idiopathic inflammatory myopathy: a registry-based study. Rheumatology. 2019;58(7):1214–20.CrossRef
160.
go back to reference Barsotti S, et al. The use of rituximab in idiopathic inflammatory myopathies: description of a monocentric cohort and review of the literature. Reumatismo. 2018;70(2):78–84.CrossRef Barsotti S, et al. The use of rituximab in idiopathic inflammatory myopathies: description of a monocentric cohort and review of the literature. Reumatismo. 2018;70(2):78–84.CrossRef
161.
go back to reference Mahler EA, et al. Rituximab treatment in patients with refractory inflammatory myopathies. Rheumatology. 2011;50(12):2206–13.CrossRef Mahler EA, et al. Rituximab treatment in patients with refractory inflammatory myopathies. Rheumatology. 2011;50(12):2206–13.CrossRef
162.
go back to reference • Stone JH, et al. Rituximab versus cyclophosphamide for ANCA-associated vasculitis. N Engl J Med. 2010;363(3):221–32. This study was one of the key randomized controlled trials showing the non-inferiority of rituximab as compared to cyclophosphamide for induction of remission of ANCA-associated vasculitis. This, along with several other studies, helped lead to the FDA approval of rituximab for the treatment of GPA and MPA in 2011. • Stone JH, et al. Rituximab versus cyclophosphamide for ANCA-associated vasculitis. N Engl J Med. 2010;363(3):221–32. This study was one of the key randomized controlled trials showing the non-inferiority of rituximab as compared to cyclophosphamide for induction of remission of ANCA-associated vasculitis. This, along with several other studies, helped lead to the FDA approval of rituximab for the treatment of GPA and MPA in 2011.
163.
go back to reference Jones RB, et al. Rituximab versus cyclophosphamide in ANCA-associated renal vasculitis. N Engl J Med. 2010;363(3):211–20.CrossRef Jones RB, et al. Rituximab versus cyclophosphamide in ANCA-associated renal vasculitis. N Engl J Med. 2010;363(3):211–20.CrossRef
164.
go back to reference Jones RB, et al. Rituximab versus cyclophosphamide in ANCA-associated renal vasculitis: 2-year results of a randomised trial. Ann Rheum Dis. 2015;74(6):1178–82.CrossRef Jones RB, et al. Rituximab versus cyclophosphamide in ANCA-associated renal vasculitis: 2-year results of a randomised trial. Ann Rheum Dis. 2015;74(6):1178–82.CrossRef
165.
go back to reference Smith RM, et al. Rituximab as therapy to induce remission after relapse in ANCA-associated vasculitis. Ann Rheum Dis. 2020;79(9):1243–9.CrossRef Smith RM, et al. Rituximab as therapy to induce remission after relapse in ANCA-associated vasculitis. Ann Rheum Dis. 2020;79(9):1243–9.CrossRef
166.
go back to reference Menditto VG, et al. Rituximab for eosinophilic granulomatosis with polyangiitis: a systematic review of observational studies. Rheumatology. 2021;60(4):1640–50.CrossRef Menditto VG, et al. Rituximab for eosinophilic granulomatosis with polyangiitis: a systematic review of observational studies. Rheumatology. 2021;60(4):1640–50.CrossRef
167.
go back to reference Akiyama M, Kaneko Y, Takeuchi T. Rituximab for the treatment of eosinophilic granulomatosis with polyangiitis: a systematic literature review. Autoimmun Rev. 2021;20(2):102737.CrossRef Akiyama M, Kaneko Y, Takeuchi T. Rituximab for the treatment of eosinophilic granulomatosis with polyangiitis: a systematic literature review. Autoimmun Rev. 2021;20(2):102737.CrossRef
168.
go back to reference Guillevin L, et al. Rituximab versus azathioprine for maintenance in ANCA-associated vasculitis. N Engl J Med. 2014;371(19):1771–80.CrossRef Guillevin L, et al. Rituximab versus azathioprine for maintenance in ANCA-associated vasculitis. N Engl J Med. 2014;371(19):1771–80.CrossRef
169.
go back to reference Terrier B, et al. Long-term efficacy of remission-maintenance regimens for ANCA-associated vasculitides. Ann Rheum Dis. 2018;77(8):1150–6.CrossRef Terrier B, et al. Long-term efficacy of remission-maintenance regimens for ANCA-associated vasculitides. Ann Rheum Dis. 2018;77(8):1150–6.CrossRef
170.
go back to reference Charles P, et al. Comparison of individually tailored versus fixed-schedule rituximab regimen to maintain ANCA-associated vasculitis remission: results of a multicentre, randomised controlled, phase III trial (MAINRITSAN2). Ann Rheum Dis. 2018;77(8):1143–9.CrossRef Charles P, et al. Comparison of individually tailored versus fixed-schedule rituximab regimen to maintain ANCA-associated vasculitis remission: results of a multicentre, randomised controlled, phase III trial (MAINRITSAN2). Ann Rheum Dis. 2018;77(8):1143–9.CrossRef
171.
go back to reference Charles P, et al. Long-term rituximab use to maintain remission of antineutrophil cytoplasmic antibody-associated vasculitis: a randomized trial. Ann Intern Med. 2020;173(3):179–87.CrossRef Charles P, et al. Long-term rituximab use to maintain remission of antineutrophil cytoplasmic antibody-associated vasculitis: a randomized trial. Ann Intern Med. 2020;173(3):179–87.CrossRef
172.
go back to reference Gopaluni S, et al. Rituximab versus azathioprine as therapy for maintenance of remission for anti-neutrophil cytoplasm antibody-associated vasculitis (RITAZAREM): study protocol for a randomized controlled trial. Trials. 2017;18(1):112.CrossRef Gopaluni S, et al. Rituximab versus azathioprine as therapy for maintenance of remission for anti-neutrophil cytoplasm antibody-associated vasculitis (RITAZAREM): study protocol for a randomized controlled trial. Trials. 2017;18(1):112.CrossRef
173.
go back to reference Sonomoto K, et al. A case of polyarteritis nodosa successfully treated by rituximab. Nihon Rinsho Meneki Gakkai Kaishi. 2008;31(2):119–23.CrossRef Sonomoto K, et al. A case of polyarteritis nodosa successfully treated by rituximab. Nihon Rinsho Meneki Gakkai Kaishi. 2008;31(2):119–23.CrossRef
174.
go back to reference Eleftheriou D, et al. Biologic therapy in primary systemic vasculitis of the young. Rheumatology. 2009;48(8):978–86.CrossRef Eleftheriou D, et al. Biologic therapy in primary systemic vasculitis of the young. Rheumatology. 2009;48(8):978–86.CrossRef
175.
go back to reference Bansal NK, Houghton KM. Cutaneous polyarteritis nodosa in childhood: a case report and review of the literature. Arthritis. 2010;2010:687547.CrossRef Bansal NK, Houghton KM. Cutaneous polyarteritis nodosa in childhood: a case report and review of the literature. Arthritis. 2010;2010:687547.CrossRef
176.
go back to reference Neel A, et al. Life-threatening hepatitis C virus-associated polyarteritis nodosa successfully treated by rituximab. J Clin Rheumatol. 2011;17(8):439–41.CrossRef Neel A, et al. Life-threatening hepatitis C virus-associated polyarteritis nodosa successfully treated by rituximab. J Clin Rheumatol. 2011;17(8):439–41.CrossRef
177.
go back to reference da Silva LS, et al. Rituximab as an alternative for patients with severe systemic vasculitis refractory to conventional therapy: report of seven cases and literature review. Rev Bras Reumatol. 2015;55(6):531–5.CrossRef da Silva LS, et al. Rituximab as an alternative for patients with severe systemic vasculitis refractory to conventional therapy: report of seven cases and literature review. Rev Bras Reumatol. 2015;55(6):531–5.CrossRef
178.
go back to reference Ribeiro E, et al. Rituximab efficacy during a refractory polyarteritis nodosa flare. Case Rep Med. 2009;2009:738293.CrossRef Ribeiro E, et al. Rituximab efficacy during a refractory polyarteritis nodosa flare. Case Rep Med. 2009;2009:738293.CrossRef
179.
go back to reference Krishnan S, Bhakuni DS, Kartik S. Rituximab in refractory cutaneous polyarteritis. Int J Rheum Dis. 2012;15(5):e127.CrossRef Krishnan S, Bhakuni DS, Kartik S. Rituximab in refractory cutaneous polyarteritis. Int J Rheum Dis. 2012;15(5):e127.CrossRef
180.
go back to reference Rees F, Yazdani R, Lanyon P. Long-term follow-up of different refractory systemic vasculitides treated with rituximab. Clin Rheumatol. 2011;30(9):1241–5.CrossRef Rees F, Yazdani R, Lanyon P. Long-term follow-up of different refractory systemic vasculitides treated with rituximab. Clin Rheumatol. 2011;30(9):1241–5.CrossRef
181.
go back to reference Campanilho-Marques R, et al. Remission induced by infliximab in a childhood polyarteritis nodosa refractory to conventional immunosuppression and rituximab. Joint Bone Spine. 2014;81(3):277–8.CrossRef Campanilho-Marques R, et al. Remission induced by infliximab in a childhood polyarteritis nodosa refractory to conventional immunosuppression and rituximab. Joint Bone Spine. 2014;81(3):277–8.CrossRef
182.
go back to reference Matsuo S, et al. The successful treatment of refractory polyarteritis nodosa using infliximab. Intern Med. 2017;56(11):1435–8.CrossRef Matsuo S, et al. The successful treatment of refractory polyarteritis nodosa using infliximab. Intern Med. 2017;56(11):1435–8.CrossRef
183.
go back to reference Rimar D, et al. Tofacitinib for polyarteritis nodosa: a tailored therapy. Ann Rheum Dis. 2016;75(12):2214–6.CrossRef Rimar D, et al. Tofacitinib for polyarteritis nodosa: a tailored therapy. Ann Rheum Dis. 2016;75(12):2214–6.CrossRef
184.
go back to reference Krusche M, et al. Tocilizumab treatment for polyarteritis nodosa. Rheumatology. 2020;59(10):e63–5.CrossRef Krusche M, et al. Tocilizumab treatment for polyarteritis nodosa. Rheumatology. 2020;59(10):e63–5.CrossRef
185.
go back to reference Shirai T, et al. Four distinct clinical phenotypes of vasculitis affecting medium-sized arteries. Scand J Rheumatol. 2019;48(4):308–14.CrossRef Shirai T, et al. Four distinct clinical phenotypes of vasculitis affecting medium-sized arteries. Scand J Rheumatol. 2019;48(4):308–14.CrossRef
186.
go back to reference Papachristodoulou E, et al. Therapeutic options for cutaneous polyarteritis nodosa: a systematic review. Rheumatology. 2021;60(9):4039–47.CrossRef Papachristodoulou E, et al. Therapeutic options for cutaneous polyarteritis nodosa: a systematic review. Rheumatology. 2021;60(9):4039–47.CrossRef
187.
go back to reference Dammacco F, et al. Pegylated interferon-alpha, ribavirin, and rituximab combined therapy of hepatitis C virus-related mixed cryoglobulinemia: a long-term study. Blood. 2010;116(3):343–53.CrossRef Dammacco F, et al. Pegylated interferon-alpha, ribavirin, and rituximab combined therapy of hepatitis C virus-related mixed cryoglobulinemia: a long-term study. Blood. 2010;116(3):343–53.CrossRef
188.
go back to reference De Vita S, et al. A randomized controlled trial of rituximab for the treatment of severe cryoglobulinemic vasculitis. Arthritis Rheum. 2012;64(3):843–53.CrossRef De Vita S, et al. A randomized controlled trial of rituximab for the treatment of severe cryoglobulinemic vasculitis. Arthritis Rheum. 2012;64(3):843–53.CrossRef
189.
go back to reference Sneller MC, Hu Z, Langford CA. A randomized controlled trial of rituximab following failure of antiviral therapy for hepatitis C virus-associated cryoglobulinemic vasculitis. Arthritis Rheum. 2012;64(3):835–42.CrossRef Sneller MC, Hu Z, Langford CA. A randomized controlled trial of rituximab following failure of antiviral therapy for hepatitis C virus-associated cryoglobulinemic vasculitis. Arthritis Rheum. 2012;64(3):835–42.CrossRef
190.
go back to reference • Kaegi C, et al. Systematic review of safety and efficacy of rituximab in treating immune-mediated disorders. Front Immunol. 2019;10:1990. This systematic review includes analysis of 118 patients with cryoglobulinemia treated with rituximab and comprises the key data showing the utility of the drug in this disease. • Kaegi C, et al. Systematic review of safety and efficacy of rituximab in treating immune-mediated disorders. Front Immunol. 2019;10:1990. This systematic review includes analysis of 118 patients with cryoglobulinemia treated with rituximab and comprises the key data showing the utility of the drug in this disease.
191.
go back to reference Saadoun D, et al. Rituximab plus belimumab in non-infectious refractory cryoglobulinemia vasculitis: a pilot study. J Autoimmun. 2021;116:102577.CrossRef Saadoun D, et al. Rituximab plus belimumab in non-infectious refractory cryoglobulinemia vasculitis: a pilot study. J Autoimmun. 2021;116:102577.CrossRef
192.
go back to reference Wink F, Houtman PM, Jansen TL. Rituximab in cryoglobulinaemic vasculitis, evidence for its effectivity: a case report and review of literature. Clin Rheumatol. 2011;30(2):293–300.CrossRef Wink F, Houtman PM, Jansen TL. Rituximab in cryoglobulinaemic vasculitis, evidence for its effectivity: a case report and review of literature. Clin Rheumatol. 2011;30(2):293–300.CrossRef
193.
go back to reference Lesniak K, et al. Noninfectious, severe cryoglobulinemic vasculitis with renal involvement - safety and efficacy of long-term treatment with rituximab. Int J Nephrol Renovasc Dis. 2021;14:267–77.CrossRef Lesniak K, et al. Noninfectious, severe cryoglobulinemic vasculitis with renal involvement - safety and efficacy of long-term treatment with rituximab. Int J Nephrol Renovasc Dis. 2021;14:267–77.CrossRef
194.
go back to reference Ferri C, et al. Treatment with rituximab in patients with mixed cryoglobulinemia syndrome: results of multicenter cohort study and review of the literature. Autoimmun Rev. 2011;11(1):48–55.CrossRef Ferri C, et al. Treatment with rituximab in patients with mixed cryoglobulinemia syndrome: results of multicenter cohort study and review of the literature. Autoimmun Rev. 2011;11(1):48–55.CrossRef
195.
go back to reference Saadoun D, et al. Rituximab plus Peg-interferon-alpha/ribavirin compared with Peg-interferon-alpha/ribavirin in hepatitis C-related mixed cryoglobulinemia. Blood. 2010;116(3):326–34.CrossRef Saadoun D, et al. Rituximab plus Peg-interferon-alpha/ribavirin compared with Peg-interferon-alpha/ribavirin in hepatitis C-related mixed cryoglobulinemia. Blood. 2010;116(3):326–34.CrossRef
196.
go back to reference Sy-Go JPT, et al. Rituximab-associated flare of cryoglobulinemic vasculitis. Kidney Int Rep. 2021;6(11):2840–9.CrossRef Sy-Go JPT, et al. Rituximab-associated flare of cryoglobulinemic vasculitis. Kidney Int Rep. 2021;6(11):2840–9.CrossRef
197.
go back to reference Desbois AC, et al. Rituximab-associated vasculitis flare: incidence, predictors, and outcome. J Rheumatol. 2020;47(6):896–902.CrossRef Desbois AC, et al. Rituximab-associated vasculitis flare: incidence, predictors, and outcome. J Rheumatol. 2020;47(6):896–902.CrossRef
198.
go back to reference Sene D, et al. Rituximab may form a complex with IgMkappa mixed cryoglobulin and induce severe systemic reactions in patients with hepatitis C virus-induced vasculitis. Arthritis Rheum. 2009;60(12):3848–55.CrossRef Sene D, et al. Rituximab may form a complex with IgMkappa mixed cryoglobulin and induce severe systemic reactions in patients with hepatitis C virus-induced vasculitis. Arthritis Rheum. 2009;60(12):3848–55.CrossRef
199.
go back to reference Fairley JL, et al. Management of cutaneous manifestations of lupus erythematosus: a systematic review. Semin Arthritis Rheum. 2020;50(1):95–127.CrossRef Fairley JL, et al. Management of cutaneous manifestations of lupus erythematosus: a systematic review. Semin Arthritis Rheum. 2020;50(1):95–127.CrossRef
200.
go back to reference da Costa RQ, et al. Assessment of response to B-cell depletion using rituximab in cutaneous lupus erythematosus. JAMA Dermatol. 2018;154(12):1432–40.CrossRef da Costa RQ, et al. Assessment of response to B-cell depletion using rituximab in cutaneous lupus erythematosus. JAMA Dermatol. 2018;154(12):1432–40.CrossRef
201.
go back to reference Vital EM, et al. Brief report: responses to rituximab suggest B cell-independent inflammation in cutaneous systemic lupus erythematosus. Arthritis Rheumatol. 2015;67(6):1586–91.CrossRef Vital EM, et al. Brief report: responses to rituximab suggest B cell-independent inflammation in cutaneous systemic lupus erythematosus. Arthritis Rheumatol. 2015;67(6):1586–91.CrossRef
202.
go back to reference Hofmann SC, et al. Effects of rituximab-based B-cell depletion therapy on skin manifestations of lupus erythematosus–report of 17 cases and review of the literature. Lupus. 2013;22(9):932–9.CrossRef Hofmann SC, et al. Effects of rituximab-based B-cell depletion therapy on skin manifestations of lupus erythematosus–report of 17 cases and review of the literature. Lupus. 2013;22(9):932–9.CrossRef
203.
go back to reference Moreno-Suarez F, Pulpillo-Ruiz A. Rituximab for the treatment of lupus erythematosus panniculitis. Dermatol Ther. 2013;26(5):415–8. Moreno-Suarez F, Pulpillo-Ruiz A. Rituximab for the treatment of lupus erythematosus panniculitis. Dermatol Ther. 2013;26(5):415–8.
Metadata
Title
Off-Label Uses of Rituximab in Dermatology
Authors
Connor Cole
Kyle T. Amber
Publication date
06-10-2022

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