Risk of clinical deterioration in patients with lupus nephritis receiving rituximab
Autor: | S Manou-Stathopoulou, M G Robson |
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Rok vydání: | 2016 |
Předmět: |
Adult
Male 0301 basic medicine medicine.medical_specialty Adolescent Cyclophosphamide Exacerbation Lupus nephritis Kidney Function Tests Young Adult 03 medical and health sciences 0302 clinical medicine Rheumatology immune system diseases hemic and lymphatic diseases Internal medicine medicine Humans Retrospective Studies 030203 arthritis & rheumatology Systemic lupus erythematosus medicine.diagnostic_test business.industry medicine.disease Lupus Nephritis Treatment Outcome 030104 developmental biology Immunology Female Steroids Rituximab Renal biopsy business Nephritis Nephrotic syndrome Immunosuppressive Agents medicine.drug |
Zdroj: | Lupus. 25:1299-1306 |
ISSN: | 1477-0962 0961-2033 |
Popis: | Rituximab is a chimeric anti-CD20 monoclonal antibody that is used as an immunosuppressive agent in cyclophosphamide refractory lupus nephritis to induce remission. Although uncontrolled case series suggest efficacy, this is not yet supported by evidence from prospective randomized controlled trials. The objective of this retrospective case series is to report the clinical outcome of seven patients who received rituximab for lupus nephritis in a single centre between 2011 and 2014. One patient had clinical evidence of an uncomplicated response to therapy. A second patient responded well with the first rituximab course, but had transient worsening of renal function and nephrotic syndrome with a second course. The other five patients all had evidence of a clinical deterioration following rituximab. Two had transient worsening of both renal function and nephrotic syndrome, with subsequent evidence of response in one of these. A fifth patient showed evidence of worsening nephrotic syndrome and renal function which then improved but with renal function remaining below the level present before rituximab. A sixth developed rapidly progressive renal failure following rituximab with active nephritis on renal biopsy and required rescue therapy with high dose steroids and cyclophosphamide. A seventh developed a transient worsening of her nephrotic syndrome and an exacerbation of extrarenal symptoms following rituximab. The two patients showing a good response had complete B cell depletion and incomplete depletion may be a factor in the deterioration seen in the other patients. Our experience suggests that rituximab therapy in lupus nephritis is not without risk and patients should be informed of this beforehand. This is particularly important in view of the uncertainty that rituximab will offer a therapeutic benefit. |
Databáze: | OpenAIRE |
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