The medical records of patients receiving cyclophosphamide for lupus n
ephritis between 1987 and 1993 at the New York University/Hospital for
Joint Diseases Lupus Study Group Institutions were retrospectively re
viewed. We identified 45 patients (38 female, seven male) who received
a mean of 9 +/- 1 (range 2-23) pulses of intravenous cyclophosphamide
for diffuse proliferative glomerulonephritis (n = 28), focal prolifer
ative glomerulonephritis (n = 7), membranous nephropathy (n = 5), mesa
ngial nephropathy with sclerosis (n = 1) or nephritis without biopsy (
n = 4). Forty-two of the 45 patients received cyclophosphamide after f
ailing steroid therapy. During a follow-up period of 52 +/- 3 months,
nine patients progressed to end-stage renal disease (ESRD) with three
additional patients experiencing a doubling of the creatinine and two
patients persistent nephrotic range proteinuria. There were no deaths
directly attributable to cyclophosphamide and no patients developed he
morrhagic cystitis or malignancy. Ten of 37 women had ceased menstruat
ing prior to cyclophosphamide therapy. Treatment-associated amenorrhea
occurred in only three patients all over 27 years of age. Intermitten
t intravenous cyclophosphamide therapy of lupus nephritis is well tole
rated and usually effective in maintaining renal function in patients
unresponsive to steroids although, in our experience, 20% of patients
developed ESRD and a total of 14 of 45 (30%) patients had unsatisfacto
ry outcomes.