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Review
. 2019 Feb 21;21(2):19.
doi: 10.1007/s11912-019-0760-z.

Pegylated Interleukin-10: Clinical Development of an Immunoregulatory Cytokine for Use in Cancer Therapeutics

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Review

Pegylated Interleukin-10: Clinical Development of an Immunoregulatory Cytokine for Use in Cancer Therapeutics

Karen Autio et al. Curr Oncol Rep. .

Abstract

Purpose of review: Interleukin-10 (IL-10) is a cytokine with anti-inflammatory properties, which induces activation and proliferation of antigen-activated intratumoral CD8+ T cells. This review discusses the evolution of pegylated IL-10 (pegilodecakin) from preclinical investigation through first-in-human studies in oncology.

Recent findings: Pegilodecakin was evaluated across multiple advanced solid tumors in a large phase 1/1b trial alone and in combination with chemotherapy or anti-PD-1 antibodies. Pegilodecakin monotherapy had immunologic and clinical activity in renal cell carcinoma (RCC) and uveal melanoma. In combination with anti-PD-1 inhibitors, pegilodecakin increased the responses in RCC and lung cancer with efficacy agnostic to PD-L1 status and tumor mutational burden. Pegilodecakin with FOLFOX had activity in pretreated pancreatic cancer, instructing the ongoing randomized phase III trial of the combination versus FOLFOX. The increased half-life of pegilodecakin enabled compelling preclinical data for IL-10 which has now been confirmed by clinical activity in a variety of cancers. The ability of pegilodecakin to both exert anti-tumor immunity and inhibit tumor-associated inflammation characterizes the uniqueness of this cytokine therapy.

Keywords: AM0010; Cytokine; IL-10; Immunotherapy; Pegilodecakin.

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References

    1. J Immunol. 2000 Sep 1;165(5):2783-9 - PubMed
    1. Oncology. 2017;93(6):367-376 - PubMed
    1. Arch Dermatol. 1999 Feb;135(2):187-92 - PubMed
    1. Gastroenterology. 1997 Aug;113(2):383-9 - PubMed
    1. J Immunol. 1991 Jul 15;147(2):528-34 - PubMed

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