Extended reports
Immunosuppressive treatment in severe connective tissue diseases:
effects of low dose intravenous cyclophosphamide
a Lupus Arthritis Research Unit, The Rayne
Institute, St Thomas's Hospital, London , b Royal Hospitals Trust, London
Correspondence to: Dr M A Khamashta, Lupus Arthritis Research Unit, The Rayne Institute, St Thomas's Hospital, London SE1 7EH.
Accepted for publication 6 June 1997
OBJECTIVE
To review our experience with low dose
intravenous pulse cyclophosphamide in the treatment of patients with
severe connective tissue diseases.
PATIENTS
Ninety patients (68F:22M) with severe
connective tissue diseases received a total of 883 cyclophosphamide
pulses with 78 of 90 patients initially having weekly 500 mg pulses for
a median of three (2-10) weeks. Diagnoses included: systemic lupus
erythematosus (SLE) (n=43); systemic vasculitides (n=42); idiopathic
inflammatory myopathies (n=4); mixed essential cryoglobulinaemic
vasculitis (n=1). The median age was 48 (range 22-76) years with a
median disease duration of 94 (18-250) months.
RESULTS
Complete or partial remission was
noted in 68 of 90 patients (75.5%) after a median follow up of 56 (5-213) months. At follow up significant median changes were noted in
SLE patients: erythrocyte sedimentation rate (ESR) from 44 to 22 mm 1st
hour; anti-dsDNA antibody concentrations from 81 to 48 IU/ml;
proteinuria from 2.5 to 1.5 g/day; serum albumin from 36 to 40 g/l;
complement C3 from 0.88 to 0.90 g/l, and C4 from 0.18 to 0.22 g/l. In
the vasculitis patients significant median changes were seen in: ESR from 44 to 15 mm 1st hour; C reactive protein (CRP) from 16 to 5 g/dl;
neutrophils from 8.55 to 4.3 × 109/l; platelets from 340 to 261 × 103/l, and haemoglobin from 12.6 to 13.2 g/dl.
Patients with Churg-Strauss syndrome, Wegener's granulomatosis, and
neuropsychiatric lupus showed the best initial response but 58% of
Wegener's patients relapsed. Median corticosteroid doses were
significantly reduced from 15 (5-60) mg to 10 (3-35) mg daily.
Adverse events: infections (7 patients), neutropenia (5), lymphopenia
(18), and haemorrhagic cystitis (1 intravenous and 2 oral
cyclophosphamide), allergies to mesna (2). None of the women at risk
had prolonged amenorrhoea. Five patients doubled their serum creatinine
and five died from sepsis (2) or severe disease (3).
CONCLUSION
Treatment of severe connective tissue
diseases with `low dose' intravenous cyclophosphamide pulses compares
in efficacy with the higher monthly doses previously advocated.
Treatment was well tolerated with fewer adverse effects and most
significantly, there were no cases of premature ovarian failure.
© 1997 by Annals of the Rheumatic Diseases
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