SHORT-TERM EFFECTS OF INTRAVENOUS PULSES OF CYCLOPHOSPHAMIDE IN THE TREATMENT OF CONNECTIVE-TISSUE DISEASE CRISIS

被引:46
作者
HAGA, HJ [1 ]
DCRUZ, D [1 ]
ASHERSON, R [1 ]
HUGHES, GRV [1 ]
机构
[1] ST THOMAS HOSP,RAYNE INST,LUPUS ARTHRIT RES UNIT,LONDON SE1 7EH,ENGLAND
关键词
D O I
10.1136/ard.51.7.885
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
A predominantly outpatient regimen of low dose intravenous cyclophosphamide was used to treat patients with serious progressive connective tissue diseases. Fifty five patients were treated with a total of 211 intravenous pulses of cyclophosphamide. Forty five patients had previously shown no response to a variety of other treatments. Low dose intravenous cyclophosphamide (500 mg) was given in 179 pulses and repeated pulses were given in most patients at weekly intervals for one to three weeks to induce disease remission. A good response was noted in 37 of 55 (67%) patients assessed four weeks after the pulses. Only 20 patients needed more than one such course of three pulses of intravenous cyclophosphamide during the observation period. The non-responders were characterised by longstanding disease and irreversible histological findings in renal and muscle biopsy samples. Patients with vasculitis, notably Wegener's granulomatosis, showed the most immediate response, and in most patients the amount of corticosteroids required was markedly reduced. In some patients steroids were completely stopped during the follow up period. The most striking observation of this effective but more conservative regimen was the low incidence of major side effects such as neutropenia and infections. It is concluded that low dose pulses of intravenous cyclophosphamide are well tolerated and are an effective treatment for patients with aggressive connective tissue diseases.
引用
收藏
页码:885 / 888
页数:4
相关论文
共 22 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]   LUPUS NEPHRITIS [J].
BALOW, JE ;
AUSTIN, HA ;
TSOKOS, GC ;
ANTONOVYCH, TT ;
STEINBERG, AD ;
KLIPPEL, JH .
ANNALS OF INTERNAL MEDICINE, 1987, 106 (01) :79-94
[3]  
BOMBARDIERI S, 1989, LANCET, V1, P1138
[4]   INFECTIOUS COMPLICATIONS OF CYCLOPHOSPHAMIDE TREATMENT FOR VASCULITIS [J].
BRADLEY, JD ;
BRANDT, KD ;
KATZ, BP .
ARTHRITIS AND RHEUMATISM, 1989, 32 (01) :45-53
[5]  
BRYANT BM, 1980, LANCET, V2, P657
[6]   CYTOTOXIC DRUGS - THEIR CLINICAL-APPLICATION TO THE RHEUMATIC DISEASES [J].
CLEMENTS, PJ ;
DAVIS, J .
SEMINARS IN ARTHRITIS AND RHEUMATISM, 1986, 15 (04) :231-254
[7]  
CUPPS TR, 1981, MAJOR PROBLEMS INTER, V21, P155
[8]   COMPARISON OF AZATHIOPRINE, CYCLOPHOSPHAMIDE, AND GOLD IN TREATMENT OF RHEUMATOID-ARTHRITIS [J].
CURREY, HLF ;
HARRIS, J ;
MASON, RM ;
WOODLAND, J ;
BEVERIDGE, T ;
ROBERTS, CJ ;
VERE, DW ;
DIXON, ASJ ;
DAVIES, J ;
OWENSMIT.B .
BMJ-BRITISH MEDICAL JOURNAL, 1974, 3 (5934) :763-766
[9]   ADRENAL GLUCOCORTICOIDS AFTER 20 YEARS . A REVIEW OF THEIR CLINICALLY RELEVANT CONSEQUENCES [J].
DAVID, DS ;
GRIECO, MH ;
CUSHMAN, P .
JOURNAL OF CHRONIC DISEASES, 1970, 22 (10) :637-+
[10]   SPECTRUM OF VASCULITIS - CLINICAL, PATHOLOGIC, IMMUNOLOGICAL, AND THERAPEUTIC CONSIDERATIONS [J].
FAUCI, AS ;
HAYNES, BF ;
KATZ, P .
ANNALS OF INTERNAL MEDICINE, 1978, 89 (05) :660-676