Aamj. Hollander et Fj. Vanderwoude, EFFICACY AND TOLERABILITY OF CONVERSION FROM CYCLOSPORINE TO AZATHIOPRINE AFTER KIDNEY-TRANSPLANTATION - A REVIEW OF THE EVIDENCE, Biodrugs, 9(3), 1998, pp. 197-210
After the introduction of cyclosporin as an immunosuppressive drug for
organ transplantation at the beginning of the 1980s, concern arose ab
out adverse effects of this new drug. Nephrotoxicity, fear of progress
ive loss of renal function with long term use of cyclosporin, a higher
incidence of lymphomas in the first studies with cyclosporin and the
high costs of the new drug led to the modification of immunosuppressiv
e regimens so that cyclosporin was replaced by azathioprine several mo
nths after renal transplantation. Short and long term follow-up of ele
ctive conversion studies demonstrated equal patient and graft survival
in the azathioprine (conversion) and cyclosporin (control) groups. Sh
ortly after conversion. renal function improved considerably and a dec
rease was found in the number of patients with hypertension and gout.
Conversion also resulted in a substantial reduction in the costs of im
munosuppressive drugs. In most studies a higher incidence of acute rej
ection was found after conversion. These rejection episodes were gener
ally reversible and at long term followup did not result in a higher i
ncidence of chronic rejection or graft loss. Elective conversion from
cyclosporin to azathioprine after kidney transplantation can be done s
afely and has beneficial effects on renal function and cardiovascular
risk factors. Conversion should also be considered fur patients with p
rolonged non-function of the graft, in cyclosporin-treated patients wi
th substantial renal or neurological toxicity persisting after cyclosp
orin dosage reduction, and in patients who cannot afford the high cost
s of cyclosporin therapy.