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Article: Long-term outcomes with rituximab as add-on therapy in severe childhood-onset lupus nephritis
Title | Long-term outcomes with rituximab as add-on therapy in severe childhood-onset lupus nephritis |
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Authors | |
Keywords | Childhood-onset lupus nephritis Dialysis Refractory Rituximab Systemic lupus erythematosus |
Issue Date | 26-Jun-2023 |
Publisher | Springer |
Citation | Pediatric Nephrology, 2023 How to Cite? |
Abstract | Background Long-term data pertaining to rituximab as add-on therapy in childhood-onset lupus nephritis (cLN) is scarce. Methods A retrospective cohort study was conducted on all patients with proliferative cLN, diagnosed <= 18 years and between 2005 and 2021, who received rituximab for LN episodes that were life/organ threatening and/or treatment resistant to standard immunosuppression. Results Fourteen patients with cLN (female, n = 10) were included, with median follow-up period of 6.9 years. LN episodes (class III, n = 1; class IV, n = 11; class IV + V, n = 2) requiring rituximab occurred at 15.6 years (IQR 12.8-17.3), urine protein:creatinine ratio was 8.2 mg/mg (IQR 3.4-10.1) and eGFR was 28 mL/min/1.73 m(2) (IQR 24-69) prior to rituximab treatment. Ten and four patients received rituximab at 1500 mg/m(2) and 750 mg/m(2), which were given at 46.5 days (IQR 19-69) after commencement of standard therapies. Treatment with rituximab resulted in improvements in proteinuria (ps < 0.001), eGFR (ps < 0.01) and serological parameters, including haemoglobin levels, complement 3 levels and anti-dsDNA antibodies, compared with baseline. Rates of complete/partial remission at 6-, 12-and 24-month post-rituximab were 28.6/42.8%, 64.2/21.4% and 69.2/15.3%. All three patients who required acute kidney replacement therapy became dialysis-free after rituximab. Relapse rate following rituximab was 0.11 episodes/patient-year. There was no lethal complication or severe infusion reaction. Hypogammaglobulinaemia was the most frequent complication (45%) but was mostly asymptomatic. Neutropenia and infections were observed in 20% and 25% of treatments. Upon last follow-up, three (21%) and two (14%) patients developed chronic kidney disease (stage 2, n = 2; stage 4; n = 1) and kidney failure, respectively. Conclusion Add-on rituximab is an effective and safe rescue therapy for cLN patients with life-/organ-threatening manifestations or treatment-resistance. |
Persistent Identifier | http://hdl.handle.net/10722/331937 |
ISSN | 2023 Impact Factor: 2.6 2023 SCImago Journal Rankings: 0.785 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Chan, Eugene Yu-hin | - |
dc.contributor.author | Wong, Sze-wa | - |
dc.contributor.author | Lai, Fiona Fung-yee | - |
dc.contributor.author | Ho, Tsz-wai | - |
dc.contributor.author | Tong, Pak-chiu | - |
dc.contributor.author | Lai, Wai-ming | - |
dc.contributor.author | Ma, Alison Lap-tak | - |
dc.contributor.author | Yap, Desmond Yat-hin | - |
dc.date.accessioned | 2023-09-28T04:59:44Z | - |
dc.date.available | 2023-09-28T04:59:44Z | - |
dc.date.issued | 2023-06-26 | - |
dc.identifier.citation | Pediatric Nephrology, 2023 | - |
dc.identifier.issn | 0931-041X | - |
dc.identifier.uri | http://hdl.handle.net/10722/331937 | - |
dc.description.abstract | <p>Background Long-term data pertaining to rituximab as add-on therapy in childhood-onset lupus nephritis (cLN) is scarce.</p><p>Methods A retrospective cohort study was conducted on all patients with proliferative cLN, diagnosed <= 18 years and between 2005 and 2021, who received rituximab for LN episodes that were life/organ threatening and/or treatment resistant to standard immunosuppression.</p><p>Results Fourteen patients with cLN (female, n = 10) were included, with median follow-up period of 6.9 years. LN episodes (class III, n = 1; class IV, n = 11; class IV + V, n = 2) requiring rituximab occurred at 15.6 years (IQR 12.8-17.3), urine protein:creatinine ratio was 8.2 mg/mg (IQR 3.4-10.1) and eGFR was 28 mL/min/1.73 m(2) (IQR 24-69) prior to rituximab treatment. Ten and four patients received rituximab at 1500 mg/m(2) and 750 mg/m(2), which were given at 46.5 days (IQR 19-69) after commencement of standard therapies. Treatment with rituximab resulted in improvements in proteinuria (ps < 0.001), eGFR (ps < 0.01) and serological parameters, including haemoglobin levels, complement 3 levels and anti-dsDNA antibodies, compared with baseline. Rates of complete/partial remission at 6-, 12-and 24-month post-rituximab were 28.6/42.8%, 64.2/21.4% and 69.2/15.3%. All three patients who required acute kidney replacement therapy became dialysis-free after rituximab. Relapse rate following rituximab was 0.11 episodes/patient-year. There was no lethal complication or severe infusion reaction. Hypogammaglobulinaemia was the most frequent complication (45%) but was mostly asymptomatic. Neutropenia and infections were observed in 20% and 25% of treatments. Upon last follow-up, three (21%) and two (14%) patients developed chronic kidney disease (stage 2, n = 2; stage 4; n = 1) and kidney failure, respectively.</p><p>Conclusion Add-on rituximab is an effective and safe rescue therapy for cLN patients with life-/organ-threatening manifestations or treatment-resistance.</p> | - |
dc.language | eng | - |
dc.publisher | Springer | - |
dc.relation.ispartof | Pediatric Nephrology | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | Childhood-onset lupus nephritis | - |
dc.subject | Dialysis | - |
dc.subject | Refractory | - |
dc.subject | Rituximab | - |
dc.subject | Systemic lupus erythematosus | - |
dc.title | Long-term outcomes with rituximab as add-on therapy in severe childhood-onset lupus nephritis | - |
dc.type | Article | - |
dc.identifier.doi | 10.1007/s00467-023-06025-6 | - |
dc.identifier.scopus | eid_2-s2.0-85162935462 | - |
dc.identifier.eissn | 1432-198X | - |
dc.identifier.isi | WOS:001020338600003 | - |
dc.identifier.issnl | 0931-041X | - |