Literature DB >> 28929820

High-dose interleukin-2 (IL-2) for the treatment of melanoma: safety considerations and future directions.

Stephen Marabondo1, Howard L Kaufman1.   

Abstract

INTRODUCTION: In 1998, high-dose interleukin-2 (IL-2) was the first immunotherapy approved for the treatment of metastatic melanoma based on durable objective responses documented in a subset of patients but widespread utilization was limited by significant toxicity. Advances in targeted therapy and the emergence of T cell checkpoint inhibitors, which can generally be given in the ambulatory setting, have further limited consideration of IL-2 for melanoma patients and the role of IL-2 in the current landscape of melanoma treatment is uncertain. Areas covered: In this review, we will describe advances in clinical diagnostic and management strategies that have improved the therapeutic window for IL-2 therapy in patients with melanoma. Further, we will describe the potential for using IL-2 in patients whose disease has progressed after other interventions or as part of combination immunotherapy approaches that are now in clinical development. We will also review the common toxicities of IL-2 therapy and their current management will be discussed. Expert opinion: High-dose IL-2 remains an important option for patients with melanoma and has an improved therapeutic window in the contemporary era. The reasons why IL-2 is not utilized more frequently and measures for enhancing its use will be detailed.

Entities:  

Keywords:  Immunotherapy; interleukin-2; melanoma; safety

Mesh:

Substances:

Year:  2017        PMID: 28929820     DOI: 10.1080/14740338.2017.1382472

Source DB:  PubMed          Journal:  Expert Opin Drug Saf        ISSN: 1474-0338            Impact factor:   4.250


  16 in total

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Journal:  BMC Cancer       Date:  2020-06-15       Impact factor: 4.430

Review 10.  Adoptive transfer of tumor-infiltrating lymphocytes in melanoma: a viable treatment option.

Authors:  Maartje W Rohaan; Joost H van den Berg; Pia Kvistborg; John B A G Haanen
Journal:  J Immunother Cancer       Date:  2018-10-03       Impact factor: 13.751

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