Journal of Clinical Oncology, Vol 7, 1875-1884, Copyright © 1989 by American Society of Clinical Oncology
Successful treatment of metastatic renal cell carcinoma with a biologically active dose of recombinant interferon-gamma
W Aulitzky, G Gastl, WE Aulitzky, M Herold, J Kemmler, B Mull, J Frick and C Huber
Department of Urology, General Hospital, Salzburg, Austria.
We tested the clinical efficacy of a biologically active dose (BAD) of
interferon (IFN)-gamma for treatment of progressive renal cell carcinoma
(RCC). Twenty-two RCC patients with disease progression subsequent to
nephrectomy were entered on a phase II clinical trial. During an initial
dose-finding phase, biochemical responses to repeated once-weekly
subcutaneous injections of 10, 100, or 500 micrograms of recombinant
IFN-gamma were tested in 16 patients. Results indicated that 100 micrograms
IFN-gamma applied once weekly was biologically active with induction of
serum beta 2-microglobulin and neopterin. Such a dose induced a nearly
maximum response of both markers lasting more than 4 days. This dose was
also associated with minimal side effects. A dose of 100 micrograms
IFN-gamma given once weekly was, therefore, subsequently given weekly for
long-term treatment. During a median time of therapy of 10 months (range, 2
to 32 months) two complete (CR; 20+, 20+ months) and four partial tumor
responses (PR; 6+, 7+, 8+, 24+ months) were seen (30% CR plus PR; 95%
confidence limits, 12% to 54%) among 20 patients evaluable for response.
Patients with refractory disease had significantly lower IFN-gamma-induced
increments of serum beta 2-microglobulin than those who achieved clinical
remission or stable disease.