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Efficacy and safety of multitarget therapy with cyclophosphamide and tacrolimus for lupus nephritis: a prospective, single-arm, single-centre, open label pilot study in Japan.
Sakai, R; Kurasawa, T; Nishi, E; Kondo, T; Okada, Y; Shibata, A; Nishimura, K; Chino, K; Okuyama, A; Takei, H; Nagasawa, H; Amano, K.
Afiliação
  • Sakai R; 1 Department of Rheumatology and Clinical Immunology, Saitama Medical University, Saitama, Japan.
  • Kurasawa T; 2 Department of Microbiology and Immunology, Keio University, Tokyo, Japan.
  • Nishi E; 1 Department of Rheumatology and Clinical Immunology, Saitama Medical University, Saitama, Japan.
  • Kondo T; 3 Institute of Rheumatology, Zenjinkai Shimin-no-Mori Hospital, Miyazaki, Japan.
  • Okada Y; 1 Department of Rheumatology and Clinical Immunology, Saitama Medical University, Saitama, Japan.
  • Shibata A; 1 Department of Rheumatology and Clinical Immunology, Saitama Medical University, Saitama, Japan.
  • Nishimura K; 1 Department of Rheumatology and Clinical Immunology, Saitama Medical University, Saitama, Japan.
  • Chino K; 1 Department of Rheumatology and Clinical Immunology, Saitama Medical University, Saitama, Japan.
  • Okuyama A; 4 Division of Rheumatology, Japan Community Health Care Organization, Saitama, Japan.
  • Takei H; 1 Department of Rheumatology and Clinical Immunology, Saitama Medical University, Saitama, Japan.
  • Nagasawa H; 1 Department of Rheumatology and Clinical Immunology, Saitama Medical University, Saitama, Japan.
  • Amano K; 1 Department of Rheumatology and Clinical Immunology, Saitama Medical University, Saitama, Japan.
Lupus ; 27(2): 273-282, 2018 Feb.
Article em En | MEDLINE | ID: mdl-28683654
ABSTRACT
Background Pulsed cyclophosphamide or mycophenolate mofetil for lupus nephritis has limited efficacy. We previously reported a case of mixed-class IV + V lupus nephritis successfully treated with cyclophosphamide and tacrolimus. This study assessed the efficacy and safety of multitarget therapy with cyclophosphamide and tacrolimus for the treatment of lupus nephritis. Methods In a prospective, single-arm, open label pilot study, we recruited 15 patients aged 18-64 years with active lupus nephritis who met the American College of Rheumatology criteria for a diagnosis of systemic lupus erythematosus (1997). The treatment protocol was a starting dose of prednisolone of 0.6-1.0 mg/kg/day for 2 weeks and then tapered to a maintenance dose, intravenous cyclophosphamide (500 mg biweekly for 3 months) and tacrolimus (3.0 mg/day). Tacrolimus was continued as maintenance therapy. Complete remission was defined as a spot urine protein/creatinine ratio of < 0.5 g/gCr with no active urine casts and a serum creatinine level that was either normal or within 30% of a previously abnormal baseline level. We retrospectively compared results for the study patients with those of 18 historical controls conventionally treated with cyclophosphamide and prednisolone. Results At baseline, the mean patient age was 41.5 ± 14.6 years (malefemale ratio 213), urine protein/creatinine ratio 3.9 ± 2.3 g/gCr and serum creatinine 84.6 ± 34.6 µmol/L. Lupus nephritis classifications included classes IV ( n = 8), III + V ( n = 1), IV + V ( n = 5) and unclassified ( n = 1). Eleven patients completed the treatment protocol and four withdrew. At 6 months, 12 of 15 (80.0%) had achieved complete remission using intention-to-treat analysis, significantly more than historical controls (seven of 18 patients, 38.9%). A transient increase in serum creatinine and gastric symptoms occurred in three cases. One patient withdrew due to cytomegalovirus antigenemia and severe diabetes, and one patient died of thrombotic microangiopathy. Conclusions Multitarget therapy with cyclophosphamide and tacrolimus can be a therapeutic option for lupus nephritis. Clinical trials registration Combination therapy of tacrolimus and intravenous cyclophosphamide for remission induction of lupus nephritis, UMIN 000004893, URL https//upload.umin.ac.jp/cgi-open-bin/ctr/ctr.cgi?function=brows&action=brows&type=summary&recptno=R000005830&language=E . Date of registration 18 January 2011.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Nefrite Lúpica / Tacrolimo / Ciclofosfamida / Ácido Micofenólico Tipo de estudo: Diagnostic_studies / Guideline / Observational_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Revista: Lupus Assunto da revista: REUMATOLOGIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Nefrite Lúpica / Tacrolimo / Ciclofosfamida / Ácido Micofenólico Tipo de estudo: Diagnostic_studies / Guideline / Observational_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged País/Região como assunto: Asia Idioma: En Revista: Lupus Assunto da revista: REUMATOLOGIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Japão
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