A randomized phase II trial of interleukin 2 and interleukin 2-interferon alpha in advanced renal cancer

G. C. Jayson, M. Middleton, S. M. Lee, L. Ashcroft, N. Thatcher

    Research output: Contribution to journalArticlepeer-review

    Abstract

    A randomized phase II trial was performed to compare the efficacy and toxicity of interleukin 2 (IL-2) with an IL-2 and interferon alpha (IFN-α) regimen for the treatment of metastatic renal carcinoma. Sixty patients with recurrent renal cell carcinoma (RCC) who had previously undergone a nephrectomy were randomized to receive three cycles of IL-2 or IL-2 with IFN-α(2b). Eighteen MU of IL-2 were administered subcutaneously on Mondays-Fridays for 3 weeks out of 4. Those patients randomized to receive the combination received the same regimen of IL-2 with 9 MU of IFN-α(2b) subcutaneously on Mondays, Wednesdays and Fridays for 3 weeks out of 4. Thirty patients were randomized to receive each arm. Twenty-nine were evaluable in each arm. Twenty-two patients received three cycles of IL-2 but only 14 patients received three cycles of IL-2/IFN-α because of the greater toxicity of the combination. The principal toxicities included nausea, fatigue and fever. There were no complete responses in either arm and only two patients who were treated with IL-2 attained a partial response. Twelve patients in each arm had stable disease and 15 patients in the IL-2 arm and 16 patients in the IL-2/IFN-α arm progressed through treatment. There were no significant differences in survival. Ten patients who received IL-2 are alive with a median follow-up of 266 days, whereas six patients who received IL-2/IFN-α are alive after a median of 278 days. The median survival from the time of identification of metastatic disease is 444 days in the IL-2 arm and 381 days in the IL-2/IFN-α arm. The IL-2/IFN-α combination is more toxic than IL-2 alone and this resulted in a reduced number of cycles of treatment. However, the median survival of the two groups was the same, suggesting that further evaluation of the IL-2/IFN-α combination should be confined to large prospective randomized clinical trials.
    Original languageEnglish
    Pages (from-to)366-369
    Number of pages3
    JournalBritish Journal of Cancer
    Volume78
    Issue number3
    Publication statusPublished - 1998

    Keywords

    • Hypernephroma
    • Interferon alpha
    • Interleukin 2
    • Renal cancer

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