'Sustained remission' in a case of SLE following megadose cyclophosphamide

被引:7
作者
Mittal, G [1 ]
Balakrishna, C [1 ]
Mangat, G [1 ]
Joshi, VR [1 ]
机构
[1] Rheumatol PD Hinduja Natl Hosp & Res Ctr, Div Rheumatol, Mambai 400016, India
关键词
SLE; nephritis; cyclophosphamide; remission;
D O I
10.1191/096120399678847326
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cytotoxic therapy, especially with cyclophosphamide in the dose 8-20 mg/kg used as intermittent pulses, has been shown to improve both patient and renal survival in systematic lupus erythematosus (SLE), but to date there is no cure for the disease. Owing to the paucity of recognisable clones, the rationale and goal of cytotoxic immunosuppressive therapy in the treatment of immune-mediated diseases as against malignancies is to suppress the aberrant inflammation and immune-mediated reactions responsible for tissue damage, without dangerously suppressing the normal host defence mechanism(s). We report the case of a patient suffering from SLE with nephritis who has remained in sustained remission over the past 8 years without any maintenance therapy following an accidental administration of a single dose of 5000 mg of intravenous cyclophosphamide (44.2 mg/kg body weight). The patient recovered fully from pancytopenia following the injection. Presently, she is asymptomatic and working gainfully. Her laboratory parameters including blood counts, urine analysis, FANA and anti-dsDNA have reverted to normal. Cyclophosphamide in the dose of 30-160 mg/kg has been safely and effectively used in various neoplastic conditions with the aim of destroying every possible tumour cell. The experience of the present case suggests that such an approach may be applicable to SLE.
引用
收藏
页码:77 / 80
页数:4
相关论文
共 34 条
[1]   THERAPY OF LUPUS NEPHRITIS - CONTROLLED TRIAL OF PREDNISONE AND CYTOTOXIC DRUGS [J].
AUSTIN, HA ;
KLIPPEL, JH ;
BALOW, JE ;
LERICHE, NGH ;
STEINBERG, AD ;
PLOTZ, PH ;
DECKER, JL .
NEW ENGLAND JOURNAL OF MEDICINE, 1986, 314 (10) :614-619
[2]  
AVASH L, 1995, P AN M AM SOC CLIN, V14, P318
[3]  
BAKE AWLV, 1994, NETH J MED, V45, P280
[4]   LUPUS NEPHRITIS [J].
BALOW, JE ;
AUSTIN, HA ;
TSOKOS, GC ;
ANTONOVYCH, TT ;
STEINBERG, AD ;
KLIPPEL, JH .
ANNALS OF INTERNAL MEDICINE, 1987, 106 (01) :79-94
[5]  
BARLOW JE, 1984, NEW ENGL J MED, V311, P491
[6]   Lupus nephritis - Discussion [J].
Berden, JHM ;
Madias, NE ;
Broumand, B ;
Klinger, M ;
Sonkodi, S ;
Nayak, KS ;
Hruby, Z .
KIDNEY INTERNATIONAL, 1997, 52 (02) :538-558
[7]   CONTROLLED TRIAL OF PULSE METHYLPREDNISOLONE VERSUS 2 REGIMENS OF PULSE CYCLOPHOSPHAMIDE IN SEVERE LUPUS NEPHRITIS [J].
BOUMPAS, DT ;
AUSTIN, HA ;
VAUGHN, EM ;
KLIPPEL, JH ;
STEINBERG, AD ;
YARBORO, CH ;
BALOW, JE .
LANCET, 1992, 340 (8822) :741-745
[8]   SYSTEMIC LUPUS-ERYTHEMATOSUS - EMERGING CONCEPTS .1. RENAL, NEUROPSYCHIATRIC, CARDIOVASCULAR, PULMONARY, AND HEMATOLOGIC DISEASE [J].
BOUMPAS, DT ;
AUSTIN, HA ;
FESSLER, BJ ;
BALOW, JE ;
KLIPPEL, JH ;
LOCKSHIN, MD .
ANNALS OF INTERNAL MEDICINE, 1995, 122 (12) :940-950
[9]  
CAMERON JS, 1979, Q J MED, V48, P1
[10]  
CAMERON JS, 1993, J NEPHROL, V6, P172