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Clinical ResearchGlomerulonephritis and Interstitial Nephritis
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Long-Term Efficacy and Safety of Repeated Rituximab to Maintain Remission in Idiopathic Childhood Nephrotic Syndrome: An International Study

Eugene Yu-hin Chan, Ellen L.M. Yu, Andrea Angeletti, Zainab Arslan, Biswanath Basu, Olivia Boyer, Chang-Yien Chan, Manuela Colucci, Guillaume Dorval, Claire Dossier, Stefania Drovandi, Gian Marco Ghiggeri, Debbie S. Gipson, Riku Hamada, Julien Hogan, Kenji Ishikura, Koichi Kamei, Markus J. Kemper, Alison Lap-tak Ma, Rulan S. Parekh, Seetha Radhakrishnan, Priya Saini, Qian Shen, Rajiv Sinha, Chantida Subun, Sharon Teo, Marina Vivarelli, Hazel Webb, Hong Xu, Hui Kim Yap and Kjell Tullus
JASN June 2022, 33 (6) 1193-1207; DOI: https://doi.org/10.1681/ASN.2021111472
Eugene Yu-hin Chan
1Paediatric Nephrology Centre, Hong Kong Children’s Hospital, Hong Kong SAR
2Department of Paediatrics and Adolescent Medicine, University of Hong Kong, Hong Kong SAR
3Department of Paediatric Nephrology, Great Ormond Street Hospital for Children, National Health Service Trust, London, United Kingdom
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Ellen L.M. Yu
4Clinical Research Center, Princess Margaret Hospital, Hong Kong SAR
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Andrea Angeletti
5Nephrology, Dialysis and Transplantation, IRCCS Istituto Giannina Gaslini, Genoa, Italy
6Laboratory of Molecular Nephrology, IRCCS Istituto Giannina Gaslini, Genova, Italy
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Zainab Arslan
3Department of Paediatric Nephrology, Great Ormond Street Hospital for Children, National Health Service Trust, London, United Kingdom
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Biswanath Basu
7Division of Pediatric Nephrology, Nilratan Sircar Medical College and Hospital, Kolkata, India
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Olivia Boyer
8Pediatric Nephrology, Reference Center for Nephrotic Syndrome in Children and Adults, Necker-Enfants Malades Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), Institut Imagine, Institut National de la Santé et de la Recherche Médicale (INSERM) U1163, Université Paris Cité, Paris, France
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Chang-Yien Chan
9Department of Paediatrics, Yong Loo Lin School of Medicine, National University of Singapore, Singapore
10Khoo Teck Puat – National University Children’s Medical Institute, National University Health System, Singapore
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Manuela Colucci
11Renal Diseases Research Unit, Genetics and Rare Diseases Research Division, Bambino Gesù Children’s Hospital, IRCCS, Rome, Italy
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Guillaume Dorval
8Pediatric Nephrology, Reference Center for Nephrotic Syndrome in Children and Adults, Necker-Enfants Malades Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), Institut Imagine, Institut National de la Santé et de la Recherche Médicale (INSERM) U1163, Université Paris Cité, Paris, France
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Claire Dossier
12Pediatric Nephrology Department, Robert Debré Hospital, APHP, Paris, France
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Stefania Drovandi
5Nephrology, Dialysis and Transplantation, IRCCS Istituto Giannina Gaslini, Genoa, Italy
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Gian Marco Ghiggeri
5Nephrology, Dialysis and Transplantation, IRCCS Istituto Giannina Gaslini, Genoa, Italy
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Debbie S. Gipson
13Division of Nephrology, Department of Pediatrics, University of Michigan, CS Mott Children’s Hospital, Ann Arbor, Michigan
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Riku Hamada
14Department of Nephrology and Rheumatology, Tokyo Metropolitan Children’s Medical Center, Tokyo, Japan
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Julien Hogan
15Department of Pediatric Nephrology, Robert-Debré Hospital, Reference Center for Nephrotic Syndrome in Children and Adults, Centre de Référence Syndrome Néphrotique de l’Enfant et de l’Adulte (CMR SNI), AP-HP, Université Paris Cité, Paris, France
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Kenji Ishikura
16Department of Pediatrics, Kitasato University School of Medicine, Tokyo, Japan
17Department of Pediatrics, Kitasato University Hospital, Tokyo, Japan
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Koichi Kamei
18Division of Nephrology and Rheumatology, National Center for Child Health and Development, Tokyo, Japan
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Markus J. Kemper
19Department of Pediatrics, Asklepios Medical School, Hamburg, Germany
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Alison Lap-tak Ma
1Paediatric Nephrology Centre, Hong Kong Children’s Hospital, Hong Kong SAR
2Department of Paediatrics and Adolescent Medicine, University of Hong Kong, Hong Kong SAR
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Rulan S. Parekh
20Division of Pediatric Nephrology, Hospital for Sick Children, Toronto, Ontario, Canada
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Seetha Radhakrishnan
20Division of Pediatric Nephrology, Hospital for Sick Children, Toronto, Ontario, Canada
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Priya Saini
20Division of Pediatric Nephrology, Hospital for Sick Children, Toronto, Ontario, Canada
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Qian Shen
21Children’s Hospital of Fudan University, National Children’s Medical Center, Shanghai, China
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Rajiv Sinha
22Pediatric Nephrology Unit, Institute of Child Health, Kolkata, India
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Chantida Subun
3Department of Paediatric Nephrology, Great Ormond Street Hospital for Children, National Health Service Trust, London, United Kingdom
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Sharon Teo
10Khoo Teck Puat – National University Children’s Medical Institute, National University Health System, Singapore
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Marina Vivarelli
23Division of Nephrology, Department of Pediatric Subspecialties, Bambino Gesù Children’s Hospital, IRCCS, Rome, Italy
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Hazel Webb
3Department of Paediatric Nephrology, Great Ormond Street Hospital for Children, National Health Service Trust, London, United Kingdom
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Hong Xu
21Children’s Hospital of Fudan University, National Children’s Medical Center, Shanghai, China
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Hui Kim Yap
9Department of Paediatrics, Yong Loo Lin School of Medicine, National University of Singapore, Singapore
10Khoo Teck Puat – National University Children’s Medical Institute, National University Health System, Singapore
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Kjell Tullus
3Department of Paediatric Nephrology, Great Ormond Street Hospital for Children, National Health Service Trust, London, United Kingdom
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Significance Statement

Children with frequently relapsing, steroid-dependent nephrotic syndrome (FRSDNS) often require multiple courses of rituximab. However, long-term effects from repeated treatments remain unknown. In this international, multicenter study of 346 children receiving 1149 courses of rituximab, the risk of relapse decreased and relapse-free survival significantly improved with repeated treatments. Important side effects, including hypogammaglobulinemia, neutropenia, and infections, were mostly mild, but significant adverse events could occur. The incidence of side effects did not increase with more treatment courses nor a higher cumulative dose of rituximab. These findings suggest that repeating rituximab therapy is an effective and reasonably safe approach for most children with FRSDNS.

Abstract

Background Long-term outcomes after multiple courses of rituximab among children with frequently relapsing, steroid-dependent nephrotic syndrome (FRSDNS) are unknown.

Methods A retrospective cohort study at 16 pediatric nephrology centers from ten countries in Asia, Europe, and North America included children with FRSDNS who received two or more courses of rituximab. Primary outcomes were relapse-free survival and adverse events.

Results A total of 346 children (age, 9.8 years; IQR, 6.6–13.5 years; 73% boys) received 1149 courses of rituximab. A total of 145, 83, 50, 28, 22, and 18 children received two, three, four, five, six, and seven or more courses, respectively. Median (IQR) follow-up was 5.9 (4.3–7.7) years. Relapse-free survival differed by treatment courses (clustered log-rank test P<0.001). Compared with the first course (10.0 months; 95% CI, 9.0 to 10.7 months), relapse-free period and relapse risk progressively improved after subsequent courses (12.0–16.0 months; HRadj, 0.03–0.13; 95% CI, 0.01 to 0.18; P<0.001). The duration of B-cell depletion remained similar with repeated treatments (6.1 months; 95% CI, 6.0 to 6.3 months). Adverse events were mostly mild; the most common adverse events were hypogammaglobulinemia (50.9%), infection (4.5%), and neutropenia (3.7%). Side effects did not increase with more treatment courses nor a higher cumulative dose. Only 78 of the 353 episodes of hypogammaglobulinemia were clinically significant. Younger age at presentation (2.8 versus 3.3 years; P=0.05), age at first rituximab treatment (8.0 versus 10.0 years; P=0.01), and history of steroid resistance (28% versus 18%; P=0.01) were associated with significant hypogammaglobulinemia. All 53 infective episodes resolved, except for one patient with hepatitis B infection and another with EBV infection. There were 42 episodes of neutropenia, associated with history of steroid resistance (30% versus 20%; P=0.04). Upon last follow-up, 332 children (96%) had normal kidney function.

Conclusions Children receiving repeated courses of rituximab for FRSDNS experience an improving clinical response. Side effects appear acceptable, but significant complications can occur. These findings support repeated rituximab use in FRSDNS.

  • rituximab
  • nephrotic syndrome
  • hypogammaglobulinemia
  • neutropenia
  • children
  • biologics
  • Copyright © 2022 by the American Society of Nephrology
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Journal of the American Society of Nephrology: 33 (6)
Journal of the American Society of Nephrology
Vol. 33, Issue 6
June 2022
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Long-Term Efficacy and Safety of Repeated Rituximab to Maintain Remission in Idiopathic Childhood Nephrotic Syndrome: An International Study
Eugene Yu-hin Chan, Ellen L.M. Yu, Andrea Angeletti, Zainab Arslan, Biswanath Basu, Olivia Boyer, Chang-Yien Chan, Manuela Colucci, Guillaume Dorval, Claire Dossier, Stefania Drovandi, Gian Marco Ghiggeri, Debbie S. Gipson, Riku Hamada, Julien Hogan, Kenji Ishikura, Koichi Kamei, Markus J. Kemper, Alison Lap-tak Ma, Rulan S. Parekh, Seetha Radhakrishnan, Priya Saini, Qian Shen, Rajiv Sinha, Chantida Subun, Sharon Teo, Marina Vivarelli, Hazel Webb, Hong Xu, Hui Kim Yap, Kjell Tullus
JASN Jun 2022, 33 (6) 1193-1207; DOI: 10.1681/ASN.2021111472

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Long-Term Efficacy and Safety of Repeated Rituximab to Maintain Remission in Idiopathic Childhood Nephrotic Syndrome: An International Study
Eugene Yu-hin Chan, Ellen L.M. Yu, Andrea Angeletti, Zainab Arslan, Biswanath Basu, Olivia Boyer, Chang-Yien Chan, Manuela Colucci, Guillaume Dorval, Claire Dossier, Stefania Drovandi, Gian Marco Ghiggeri, Debbie S. Gipson, Riku Hamada, Julien Hogan, Kenji Ishikura, Koichi Kamei, Markus J. Kemper, Alison Lap-tak Ma, Rulan S. Parekh, Seetha Radhakrishnan, Priya Saini, Qian Shen, Rajiv Sinha, Chantida Subun, Sharon Teo, Marina Vivarelli, Hazel Webb, Hong Xu, Hui Kim Yap, Kjell Tullus
JASN Jun 2022, 33 (6) 1193-1207; DOI: 10.1681/ASN.2021111472
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  • rituximab
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  • neutropenia
  • children
  • biologics

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