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Efficacy and safety of obinutuzumab in systemic lupus erythematosus patients with secondary non-response to rituximab.
Arnold, Jack; Dass, Shouvik; Twigg, Sarah; Jones, Colin H; Rhodes, Ben; Hewins, Peter; Chakravorty, Mithun; Courtney, Phil; Ehrenstein, Michael; Md Yusof, Md Yuzaiful; Vital, Edward M.
Afiliação
  • Arnold J; Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds.
  • Dass S; NIHR Leeds Biomedical Research Centre, Leeds Teaching Hospitals NHS Trust, Leeds.
  • Twigg S; Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds.
  • Jones CH; NIHR Leeds Biomedical Research Centre, Leeds Teaching Hospitals NHS Trust, Leeds.
  • Rhodes B; Bradford Teaching Hospitals NHS Foundation Trust, Bradford.
  • Hewins P; York Teaching Hospitals NHS Foundation Trust, York.
  • Chakravorty M; University Hospitals Birmingham NHS Foundation Trust, Birmingham.
  • Courtney P; University Hospitals Birmingham NHS Foundation Trust, Birmingham.
  • Ehrenstein M; Nottingham University Hospitals NHS Trust, Nottingham.
  • Md Yusof MY; Nottingham University Hospitals NHS Trust, Nottingham.
  • Vital EM; University College London, London, UK.
Rheumatology (Oxford) ; 61(12): 4905-4909, 2022 11 28.
Article em En | MEDLINE | ID: mdl-35266512
OBJECTIVES: Secondary inefficacy with infusion reactions and anti-drug antibodies (secondary non-depletion nonresponse, 2NDNR) occurs in 14% of SLE patients receiving repeated rituximab courses. We evaluated baseline clinical characteristics, efficacy and safety of obinutuzumab, a next-generation humanized type-2 anti-CD20 antibody licensed for haematological malignancies in SLE patients with 2NDNR to rituximab. METHODS: We collated data from SLE patients receiving obinutuzumab for secondary non-response to rituximab in BILAG centres. Disease activity was assessed using BILAG-2004, SLEDAI-2K and serology before, and 6 months after, obinutuzumab 2× 1000 mg infusions alongside methylprednisolone 100 mg. RESULTS: All nine patients included in the study received obinutuzumab with concomitant oral immunosuppression. At 6 months post-obinutuzumab, there were significant reductions in median SLEDAI-2K from 12 to 6 (P = 0.014) and total BILAG-2004 score from 21 to 2 (P = 0.009). Complement C3 and dsDNA titres improved significantly (both P = 0.04). Numerical, but not statistically significant improvements were seen in C4 levels. Of 8/9 patients receiving concomitant oral prednisolone at baseline (all >10 mg/day), 5/8 had their dose reduced at 6 months. Four of nine patients were on 5 mg/day and were in Lupus Low Disease Activity State following obinutuzumab. After obinutuzumab, 6/9 patients with peripheral B cell data achieved complete depletion, including 4/4 assessed with highly sensitive assays. Of the nine patients, one obinutuzumab non-responder required CYC therapy. One unvaccinated patient died from COVID-19. CONCLUSIONS: Obinutuzumab appears to be effective and steroid-sparing in renal and non-renal SLE patients with secondary non-response to rituximab. These patients have severe disease with few treatment options but given responsiveness to B cell depletion, switching to humanized type-2 anti-CD20 therapy is a logical approach.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: COVID-19 / Lúpus Eritematoso Sistêmico Limite: Humans Idioma: En Revista: Rheumatology (Oxford) Assunto da revista: REUMATOLOGIA Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: COVID-19 / Lúpus Eritematoso Sistêmico Limite: Humans Idioma: En Revista: Rheumatology (Oxford) Assunto da revista: REUMATOLOGIA Ano de publicação: 2022 Tipo de documento: Article