Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/38898
Conference/Presentation Title: Induction and maintenance treatment of proliferative lupus nephritis: An updated Cochrane review. [Lupus Science and Medicine]
Authors: Strippoli G.F.M.;Palmer S.C.;Craig J.C.;Webster A.C.;Henderson L.K.;Masson P.;Tunnicliffe D.J.;Tong A.;Singh-Grewal D.;Flanc R.;Roberts M.A.
Monash Health Department(s): Nephrology
Institution: (Tunnicliffe, Craig, Webster, Masson, Tong, Strippoli) University of Sydney, Sydney School of Public Health, Sydney, Australia (Tunnicliffe, Craig, Webster, Masson, Tong, Strippoli) Children's Hospital at Westmead, Centre for Kidney Research, Sydney, Australia (Palmer) University of Otago, Department of Medicine, Christchurch, New Zealand (Webster) Westmead Institute, Centre for Transplant and Renal Research, Sydney, Australia (Henderson) Royal Infirmary of Edinburgh, Department of Renal Medicine, Edinburgh, United Kingdom (Masson) University of Edinburgh, Department of Medicine, University of Edinburgh, United Kingdom (Singh-Grewal) University of Sydney, Sydney Medical School, Sydney, Australia (Singh-Grewal) University of New South Wales, Faculty of Medicine, Sydney, Australia (Singh-Grewal) Sydney Children's Hospital Network, Department of Rheumatology, Sydney, Australia (Flanc) Monash Medical Centre, Department of Nephrology, Melbourne, Australia (Roberts) Eastern Health Clinical School- Monash University, Department of Nephrology, Box Hill- Australia, Australia (Strippoli) University of Bari, Department of Emergency and Organ Transplantation, Bari, Italy (Strippoli) Diaverum, Medical Scientific Office, Lund, Sweden
Presentation/Conference Date: 28-Sep-2018
Copyright year: 2017
Publisher: BMJ Publishing Group
Publication information: Lupus Science and Medicine. Conference: 12th International Congress on Systemic Lupus Erythematosus, LUPUS 2017 and the 7th Asian Congress on Autoimmunity, ACA 2017. Melbourne, VIC Australia. 4 (Supplement 1) (pp A117-A118), 2017. Date of Publication: March 2017.
Abstract: Background and aims Pharmacological treatments have improved survival in lupus nephritis. However, intravenous cyclophosphamide as first-line therapy has considerable toxicity and lacks evidence of efficacy to prevent end-stage kidney disease. The comparative efficacy of newer strategies compared with intravenous cyclophosphamide remains unclear. Methods We updated a random-effects meta-analysis of randomised controlled trials on induction and maintenance therapy for proliferative lupus nephritis. Evidence quality was assessed using GRADE. Results 59 trials (4465 participants) were eligible, including nine new trials. Compared with intravenous cyclophosphamide, mycophenolate mofetil (MMF) incurred similar risks of complete remission, mortality, or major infection, while risks of alopecia and ovarian failure were lower (Table 1) (evidence quality=moderate). There was no evidence combined MMF and tacrolimus had different effects on complete remission or major infection than intravenous cyclophosphamide (Table 1) (evidence quality=low-very low). In maintenance therapy (Table 2), MMF decreased risks of disease relapse compared to azathioprine (evidence quality=moderate), although there was no evidence of different effects between maintenance therapies on mortality, end-stage kidney disease, or major infection (evidence quality = very low -low). Conclusions MMF is as effective as intravenous cyclophosphamide in inducing remission in patients with proliferative lupus nephritis, with lower risks of alopecia and ovarian failure, although comparative effects of treatment on end-stage kidney disease and mortality remain uncertain. MMF is the most effective maintenance treatment to prevent relapse. (Table Presented) .
Conference Start Date: 2017-03-26
Conference End Date: 2017-03-29
DOI: http://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1136/lupus-2017-000215.254
ISSN: 2053-8790
URI: https://repository.monashhealth.org/monashhealthjspui/handle/1/38898
Type: Conference Abstract
Type of Clinical Study or Trial: Systematic review and/or meta-analysis
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