Your browser doesn't support javascript.
loading
Rituximab in maintaining remission in adults with podocytopathy.
Ramachandran, Raja; Bharati, Joyita; Nada, Ritambhra; Minz, Ranjana; Kohli, Harbir S.
Afiliação
  • Ramachandran R; Department of Nephrology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Bharati J; Department of Nephrology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Nada R; Department of Histopathology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Minz R; Department of Immunopathology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
  • Kohli HS; Department of Nephrology, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Nephrology (Carlton) ; 25(8): 616-624, 2020 Aug.
Article em En | MEDLINE | ID: mdl-32297386
ABSTRACT
Rituximab is currently used after the conventional agents have failed in the management of steroid-dependent (SD)/ steroid-resistant (SR) podocytopathies and have a safer toxicity profile. We report 53 adults with podocytopathies who were managed effectively with CD19-targeted rituximab therapy.

METHODS:

This was a prospective study carried out at a tertiary care centre in India between January 2014 and June 2019. Adults between 16 and 60 years with SD, frequently relapsing (FR), and SR nephrotic syndrome (NS) due to podocytopathy received rituximab in a CD19-targeted approach. PRIMARY

OUTCOME:

Percentage of patients who were in remission at 6 and 12 months. Secondary

outcome:

Percentage of patients in remission at the last follow-up, rituximab dose and adverse events of rituximab therapy.

RESULTS:

Fifty-three adults with SD/FR/SR NS received CD19-targeted rituximab. The median age at the time of first rituximab injection was 30.09 ± 13.21 (16.53) years. At the time of first rituximab infusion, all patients were in remission with steroids and/or calcineurin inhibitors (CNIs). Fifty (94.33%) patients were in remission at the end of 6 and 12 months and the last follow-up (median 36 months). The mean total dose of rituximab at 1 year was 788.7 ± 128.1 (6 001 100) mg. At last follow-up (median 36 months), 42 (79%) patients did not require any additional CNI or steroids therapy. No serious adverse events to rituximab were noted.

CONCLUSION:

CD19-targeted rituximab therapy is safe and efficacious in the management of SD/SR adult podocytopathy. Also, rituximab is effective in maintaining remission in treatment naïve adult SD or FR podocytopathy.
Assuntos
Palavras-chave

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Indução de Remissão / Glomerulosclerose Segmentar e Focal / Rituximab / Nefrose Lipoide / Síndrome Nefrótica Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male País/Região como assunto: Asia Idioma: En Revista: Nephrology (Carlton) Assunto da revista: NEFROLOGIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Índia

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Indução de Remissão / Glomerulosclerose Segmentar e Focal / Rituximab / Nefrose Lipoide / Síndrome Nefrótica Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male País/Região como assunto: Asia Idioma: En Revista: Nephrology (Carlton) Assunto da revista: NEFROLOGIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Índia