R. Schiel et al., CYCLOSPORINE AND PLASMAPHERESIS IN TREATMENT OF PROGRESSIVE SYSTEMIC LUPUS-ERYTHEMATOSUS (PSLE), Transfusion science, 18(1), 1997, pp. 91-97
The prognosis of patients suffering from progressive systemic lupus er
ythematosus (pSLE) is poor, despite treatment with intensive drug regi
mens with combinations of corticosteroids, azathioprine and cyclophosp
ahmide. Side-effects such as infections and malignomas often occur. In
the present trial, 21 patients (four male, 17 female, aged 37.9 +/- 1
2.8), suffering from pSLE for 9.4 +/- 2.6 years, were treated for 2.3
+/- 1.8 years with drug regimens as mentioned above. Then, over a peri
od of 6.4 +/- 2.6 (range 1-8) years, in addition to conventional thera
pies, cyclosporin (2.5 +/- 0.6 mg/kg body wt/d) and, in active stages
of the disease with extremely high concentrations of anti-ds-DNA-, ant
i-nuclear antibodies and circulating immunocomplexes, plasmapheresis (
therapeutic plasma exchange (TPE)) have been applied. Compared with pr
evious treatment modalities, significantly (P < 0.05) more effective a
nd rapid reduction of antibodies was achieved. Clinical symptoms impro
ved within 2 to 4 weeks. Under the new therapeutic regimen all patient
s reported increased performance and a better quality of life. After 5
to 48 (17.5 +/- 13.8) months, cyclosporin was established as mono-the
rapy for 8/21 patients. In] the other cases, corticosteroids, azathiop
rine and cyclophosphamide were reduced by 40 to 100%. No severe side-e
ffects were seen. In acute stages of pSLE and in forms with persistent
ly high antibody levels, the addition of TPE to conventional therapy w
as very effective, with regard to improving both clinical and laborato
ry parameters. (C) 1997 Elsevier Science Ltd.