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Interleukin-2 Based Therapy for Kidney Cancer

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Part of the book series: Cancer Treatment and Research ((CTAR,volume 116))

Abstract

Interleukin-2 (IL-2) is a 15 kDa glycoprotein, originally characterized as T-cell growth factor,’ and is produced in response to T-cell activation. Interleukin-2 binds to cells through T-cell receptors which are up-regulated with activation, and through these receptors, signals clonal expansion of T-cells, with specific and non-specific immunity, and expansion of natural killer (NK) cells, all with cytotoxic activity.2In addition, secondary cytokines are released, such as interferon-gamma, tumor necrosis factor, and interleukin-1, among others.’ Recombinant DNA technology has allowed the production of IL-2 in large quantities, allowing for clinical investigation of this agent.’ The most generally used formulation is that produced by Chiron, Proleukin®. Subsequent to this, clinical trials have demonstrated efficacy in the treatment of metastatic renal cell cancer and melanoma, and IL-2 was approved for these indications. The initial approval was for therapy with high dose IL-2, to be described below, which remains the gold standard for IL-2 administration in renal cell causes and melanoma. This approval is based on the durability of the responses that are produced. However, due to the toxicity and the need for patient selectivity with high dose IL-2, a variety of regimens exploring lower doses and different schedules and combinations have been investigated. These will be summarized.

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Dutcher, J.P. (2003). Interleukin-2 Based Therapy for Kidney Cancer. In: Figlin, R.A. (eds) Kidney Cancer. Cancer Treatment and Research, vol 116. Springer, Boston, MA. https://doi.org/10.1007/978-1-4615-0451-1_9

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