Journal of Clinical Oncology, Vol 12, 1572-1576, Copyright © 1994 by American Society of Clinical Oncology
Randomized comparison of high-dose and low-dose intravenous interleukin- 2 for the therapy of metastatic renal cell carcinoma: an interim report
JC Yang, SL Topalian, D Parkinson, DJ Schwartzentruber, JS Weber, SE Ettinghausen, DE White, SM Steinberg, DJ Cole and HI Kim
Surgery Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.
PURPOSE: A randomized prospective study was performed to compare the
efficacy and toxicity of high-dose intravenous bolus interleukin-2 (IL- 2)
and a lower-dose intravenous bolus regimen for the treatment of metastatic
renal cell carcinoma (RCC). PATIENTS AND METHODS: Between March 1991 and
April 1993, 125 patients with metastatic RCC were randomized to receive
IL-2 by intravenous bolus every 8 hours at either 720,000 IU/kg (high-dose)
or 72,000 IU/kg (low-dose) to the maximum- tolerated number of doses (or a
maximum of 15 doses). After approximately 7 to 10 days, both treatment
groups were re-treated with a second identical cycle of therapy. Those
patients who were stable or responding to treatment 5 to 6 weeks later went
on to receive re- treatment with another course (two cycles) of therapy.
Response rates and toxicity were determined for the two treatment arms.
RESULTS: One hundred twenty-five patients received a total of 208 courses
of therapy. Sixty patients were randomized to receive low-dose, and 65 to
receive high-dose IL-2. There were no treatment-related deaths in either
arm. There was a greater incidence of grade III or IV thrombocytopenia,
malaise, and hypotension in patients who received high-dose IL-2, while
patients who received low-dose IL-2 had significantly more infections.
Three percent of treatment courses with low-dose IL-2 required vasopressor
support, compared with 52% of courses with high-dose IL-2. Patients who
received low-dose IL-2 had a 7% complete response (CR) and an 8% partial
response (PR) rate, and patients who received high-dose IL-2 had a 3% CR
and a 17% PR rate. CONCLUSION: Low-dose intravenous bolus IL-2 represents
an effective regimen for the treatment of metastatic RCC, with preliminary
results comparable to those observed with high-dose IL-2. Low-dose IL-2 can
be administered with significantly fewer complications, reduced use of
vasopressor support, and fewer admissions to an intensive care unit (ICU).

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