Treatment of severe lupus nephritis: effect of prolonged and intermittent intravenous cyclophosphamide

Bibliographic Details
Main Author: V. Morales, José
Publication Date: 2022
Other Authors: Veronese, Francisco J., Weber, Raimar, L. Klamt, Charles, Berdichewisk, Roberto
Format: Article
Language: por
Source: Clinical and Biomedical Research
Download full: https://seer.ufrgs.br/index.php/hcpa/article/view/125381
Summary: OBJECTIVE: Intravenous cyclophosphamide is widely used in the treatment of lupus nephritis. In order to analyze long-term outcome in patients with severe lupus nephritis, we studied 54 patients treated with cyclophosphamide at our services between 1989 and 1999. MATERIALS AND METHODS: Our study included 42 patients. According to World Health Organization classification, the initial renal biopsy indicated lupus nephritis class III in 16.7% patients and class IV in 83.3%. The average serum creatinine and proteinuria at the beginning of treatment were, respectively 3.1 ± 2.5 mg/dl and 7.2 ± 5.4 g/24h/1.73m2. Eighty-eight percent of patients had nephrotic range proteinuria and 83.3% had serum creatinine levels higher than 1.2mg/dl. The mean duration of nephritis before treatment was 10 months; however, in 52% of patients it was less than 6 months. Average follow-up time from the beginning of treatment to outcome (end-stage renal disease or death) was 72.2 ± 36.3 months. Patients received immunosuppressive therapy according to the National Institutes of Health protocol and were classified, according to clinical and laboratory response into complete remission, partial remission, or treatment failure. RESULTS: Total or partial remission was achieved in 70% of patients by the end of the first year; 62.5 % of patients were kept in remission up to the third year. The 3, 5, and 10-year actuarial renal survival rates were of 90.2%, 90.2%, and 77.67%, respectively. One patient died and 5 had to start hemodialysis. The adverse effects of immunosuppression were respiratory infection (19.0%), Herpes Zoster (7.1%), temporary (9.5%) and permanent (2.3%) amenorrhea, avascular necrosis of the femoral head (4.7%), and sepsis (2.3%). Neither hemorrhagic cystitis nor neoplasia were observed during follow-up. CONCLUSIONS: We concluded that intravenous cyclophosphamide was effective in the control of acute lupus nephritis and in the maintenance of long-term renal function without serious adverse events. 
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spelling Treatment of severe lupus nephritis: effect of prolonged and intermittent intravenous cyclophosphamideTratamento da nefropatia lúpica severa: efeito da ciclofosfamida endovenosa prolongada e intermitenteNefropatia lúpicalúpus eritematoso sistêmicociclofosfamidaimunossupressoresLupus nephritissystemic lupus erythematosuscyclophosphamideimmunosuppressionOBJECTIVE: Intravenous cyclophosphamide is widely used in the treatment of lupus nephritis. In order to analyze long-term outcome in patients with severe lupus nephritis, we studied 54 patients treated with cyclophosphamide at our services between 1989 and 1999. MATERIALS AND METHODS: Our study included 42 patients. According to World Health Organization classification, the initial renal biopsy indicated lupus nephritis class III in 16.7% patients and class IV in 83.3%. The average serum creatinine and proteinuria at the beginning of treatment were, respectively 3.1 ± 2.5 mg/dl and 7.2 ± 5.4 g/24h/1.73m2. Eighty-eight percent of patients had nephrotic range proteinuria and 83.3% had serum creatinine levels higher than 1.2mg/dl. The mean duration of nephritis before treatment was 10 months; however, in 52% of patients it was less than 6 months. Average follow-up time from the beginning of treatment to outcome (end-stage renal disease or death) was 72.2 ± 36.3 months. Patients received immunosuppressive therapy according to the National Institutes of Health protocol and were classified, according to clinical and laboratory response into complete remission, partial remission, or treatment failure. RESULTS: Total or partial remission was achieved in 70% of patients by the end of the first year; 62.5 % of patients were kept in remission up to the third year. The 3, 5, and 10-year actuarial renal survival rates were of 90.2%, 90.2%, and 77.67%, respectively. One patient died and 5 had to start hemodialysis. The adverse effects of immunosuppression were respiratory infection (19.0%), Herpes Zoster (7.1%), temporary (9.5%) and permanent (2.3%) amenorrhea, avascular necrosis of the femoral head (4.7%), and sepsis (2.3%). Neither hemorrhagic cystitis nor neoplasia were observed during follow-up. CONCLUSIONS: We concluded that intravenous cyclophosphamide was effective in the control of acute lupus nephritis and in the maintenance of long-term renal function without serious adverse events. OBJETIVOS: A ciclofosfamida intravenosa é amplamente usada no tratamento da nefrite lúpica. Para analisar os desfechos a longo prazo, estudamos 54 pacientes tratados com ciclofosfamida no período compreendido entre 1989 e 1999. MATERIAIS E MÉTODOS: Quarenta e dois pacientes foram incluídos no estudo. As biópsias renais revelaram, de acordo com a classificação da Organização Mundial de Saúde, nefrite lúpica classe III em 16,7% dos pacientes e classe IV em 83,3%. No início do tratamento, médias de creatinina sérica e proteinúria foram, respectivamente de 3,1 ± 2,5 mg/dl e 7,2 ± 5,4g/24h/1.73m2. Oitenta e oito por cento dos pacientes tinham proteinúria nefrótica, e em 83,3% a creatinina sérica era maior que 1,2 mg/dl. A duração média da nefrite anterior ao tratamento era de 10 meses, porém em 52% dos pacientes a duração era inferior a 6 meses. O seguimento médio desde o início do tratamento até os desfechos avaliados (insuficiência renal crônica terminal ou morte) foi de 72,2 ± 36,3 meses. Os pacientes receberam tratamento imunossupressor de acordo com o protocolo do National Institutes of Health dos Estados Unidos. Os pacientes foram classificados de acordo com a resposta clínico-laboratorial em remissãocompleta, remissão parcial ou falha do tratamento. RESULTADOS: Remissão total ou parcial foi alcançada em 70% dos pacientes no final do primeiro ano, e 62,5 % se mantiveram em remissão no final do terceiro ano. A sobrevida renal atuarial no 3º, 5º e 10º anos foram de 90,2%, 90,2% e 77,67%, respectivamente. Um paciente evoluiu para óbito e cinco necessitaram iniciar hemodiálise. Efeitos adversos do tratamento imunossupressor foram infecção respiratória (19,0%), Herpes Zoster (7,1%), amenorréia transitória (9,5%) e permanente (2,3%), necrose avascular de fêmur (4,7%) e sepse (2,3%). No período de seguimento não foi observada a ocorrência de cistite hemorrágica ou neoplasia. CONCLUSÕES: Concluímos que ciclofosfamida endovenosa foi efetiva no controle da nefrite lúpica aguda e na manutenção da função renal a longo prazo, sem a ocorrência de efeitos adversos sérios.HCPA/FAMED/UFRGS2022-06-23info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionPeer-reviewed ArticleAvaliado por Paresapplication/pdfhttps://seer.ufrgs.br/index.php/hcpa/article/view/125381Clinical & Biomedical Research; Vol. 20 No. 3 (2000): Revista HCPAClinical and Biomedical Research; v. 20 n. 3 (2000): Revista HCPA2357-9730reponame:Clinical and Biomedical Researchinstname:Universidade Federal do Rio Grande do Sul (UFRGS)instacron:UFRGSporhttps://seer.ufrgs.br/index.php/hcpa/article/view/125381/85234http://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessV. Morales, José Veronese, Francisco J. Weber, Raimar L. Klamt, Charles Berdichewisk, Roberto 2022-09-16T16:33:15Zoai:seer.ufrgs.br:article/125381Revistahttps://www.seer.ufrgs.br/index.php/hcpaPUBhttps://seer.ufrgs.br/index.php/hcpa/oai||cbr@hcpa.edu.br2357-97302357-9730opendoar:2022-09-16T16:33:15Clinical and Biomedical Research - Universidade Federal do Rio Grande do Sul (UFRGS)false
dc.title.none.fl_str_mv Treatment of severe lupus nephritis: effect of prolonged and intermittent intravenous cyclophosphamide
Tratamento da nefropatia lúpica severa: efeito da ciclofosfamida endovenosa prolongada e intermitente
title Treatment of severe lupus nephritis: effect of prolonged and intermittent intravenous cyclophosphamide
spellingShingle Treatment of severe lupus nephritis: effect of prolonged and intermittent intravenous cyclophosphamide
V. Morales, José
Nefropatia lúpica
lúpus eritematoso sistêmico
ciclofosfamida
imunossupressores
Lupus nephritis
systemic lupus erythematosus
cyclophosphamide
immunosuppression
title_short Treatment of severe lupus nephritis: effect of prolonged and intermittent intravenous cyclophosphamide
title_full Treatment of severe lupus nephritis: effect of prolonged and intermittent intravenous cyclophosphamide
title_fullStr Treatment of severe lupus nephritis: effect of prolonged and intermittent intravenous cyclophosphamide
title_full_unstemmed Treatment of severe lupus nephritis: effect of prolonged and intermittent intravenous cyclophosphamide
title_sort Treatment of severe lupus nephritis: effect of prolonged and intermittent intravenous cyclophosphamide
author V. Morales, José
author_facet V. Morales, José
Veronese, Francisco J.
Weber, Raimar
L. Klamt, Charles
Berdichewisk, Roberto
author_role author
author2 Veronese, Francisco J.
Weber, Raimar
L. Klamt, Charles
Berdichewisk, Roberto
author2_role author
author
author
author
dc.contributor.author.fl_str_mv V. Morales, José
Veronese, Francisco J.
Weber, Raimar
L. Klamt, Charles
Berdichewisk, Roberto
dc.subject.por.fl_str_mv Nefropatia lúpica
lúpus eritematoso sistêmico
ciclofosfamida
imunossupressores
Lupus nephritis
systemic lupus erythematosus
cyclophosphamide
immunosuppression
topic Nefropatia lúpica
lúpus eritematoso sistêmico
ciclofosfamida
imunossupressores
Lupus nephritis
systemic lupus erythematosus
cyclophosphamide
immunosuppression
description OBJECTIVE: Intravenous cyclophosphamide is widely used in the treatment of lupus nephritis. In order to analyze long-term outcome in patients with severe lupus nephritis, we studied 54 patients treated with cyclophosphamide at our services between 1989 and 1999. MATERIALS AND METHODS: Our study included 42 patients. According to World Health Organization classification, the initial renal biopsy indicated lupus nephritis class III in 16.7% patients and class IV in 83.3%. The average serum creatinine and proteinuria at the beginning of treatment were, respectively 3.1 ± 2.5 mg/dl and 7.2 ± 5.4 g/24h/1.73m2. Eighty-eight percent of patients had nephrotic range proteinuria and 83.3% had serum creatinine levels higher than 1.2mg/dl. The mean duration of nephritis before treatment was 10 months; however, in 52% of patients it was less than 6 months. Average follow-up time from the beginning of treatment to outcome (end-stage renal disease or death) was 72.2 ± 36.3 months. Patients received immunosuppressive therapy according to the National Institutes of Health protocol and were classified, according to clinical and laboratory response into complete remission, partial remission, or treatment failure. RESULTS: Total or partial remission was achieved in 70% of patients by the end of the first year; 62.5 % of patients were kept in remission up to the third year. The 3, 5, and 10-year actuarial renal survival rates were of 90.2%, 90.2%, and 77.67%, respectively. One patient died and 5 had to start hemodialysis. The adverse effects of immunosuppression were respiratory infection (19.0%), Herpes Zoster (7.1%), temporary (9.5%) and permanent (2.3%) amenorrhea, avascular necrosis of the femoral head (4.7%), and sepsis (2.3%). Neither hemorrhagic cystitis nor neoplasia were observed during follow-up. CONCLUSIONS: We concluded that intravenous cyclophosphamide was effective in the control of acute lupus nephritis and in the maintenance of long-term renal function without serious adverse events. 
publishDate 2022
dc.date.none.fl_str_mv 2022-06-23
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
Peer-reviewed Article
Avaliado por Pares
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://seer.ufrgs.br/index.php/hcpa/article/view/125381
url https://seer.ufrgs.br/index.php/hcpa/article/view/125381
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv https://seer.ufrgs.br/index.php/hcpa/article/view/125381/85234
dc.rights.driver.fl_str_mv http://creativecommons.org/licenses/by/4.0
info:eu-repo/semantics/openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by/4.0
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv HCPA/FAMED/UFRGS
publisher.none.fl_str_mv HCPA/FAMED/UFRGS
dc.source.none.fl_str_mv Clinical & Biomedical Research; Vol. 20 No. 3 (2000): Revista HCPA
Clinical and Biomedical Research; v. 20 n. 3 (2000): Revista HCPA
2357-9730
reponame:Clinical and Biomedical Research
instname:Universidade Federal do Rio Grande do Sul (UFRGS)
instacron:UFRGS
instname_str Universidade Federal do Rio Grande do Sul (UFRGS)
instacron_str UFRGS
institution UFRGS
reponame_str Clinical and Biomedical Research
collection Clinical and Biomedical Research
repository.name.fl_str_mv Clinical and Biomedical Research - Universidade Federal do Rio Grande do Sul (UFRGS)
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