High dose interleukin-2 (Aldesleukin) - expert consensus on best management practices-2014

dc.contributor.authorDutcher, Janice P.
dc.contributor.authorSchwartzentruber, Douglas J.
dc.contributor.authorKaufman, Howard L.
dc.contributor.authorAgarwala, Sanjiv S.
dc.contributor.authorTarhini, Ahmad A.
dc.contributor.authorLowder, James N.
dc.contributor.authorAtkins, Michael B.
dc.contributor.departmentSurgery, School of Medicineen_US
dc.date.accessioned2020-03-24T12:56:51Z
dc.date.available2020-03-24T12:56:51Z
dc.date.issued2014
dc.description.abstractInterleukin-2 (IL-2) was historically one of the few treatments for adults with stage IV solid tumors that could produce complete responses (CRs) that were often durable for decades without further therapy. The majority of complete responders with metastatic renal cell carcinoma (mRCC) and metastatic melanoma (mM) could probably be classified as "cures". Recent publications have suggested improved efficacy, perhaps due to improved patient selection based on a better understanding of clinical features predicting outcomes. Guidelines for clinical management were established from experience at the National Cancer Institute (NCI) and an affiliation of institutions known as the Cytokine Working Group (CWG), who were among the first to utilize HD IL-2 treatment outside of the NCI. As new centers have opened, further management variations have emerged based upon center-specific experience, to optimize administration of IL-2 and provide high quality care for patients at each individual site. Twenty years of evolution in differing environments has led to a plethora of clinical experience and effective management approaches. The goal of this review is to summarize the spectrum of HD IL-2 treatment approaches, describing various effective strategies that incorporate newer adjunctive treatments for managing the side effects of IL-2 in patients with mRCC and mM. The goal for IL-2 therapy is typically to administer the maximum number of doses of IL-2 without putting the patient at unacceptable risk for severe, irreversible toxicity. This review is based upon a consensus meeting and includes guidelines on pre-treatment screening, criteria for administration and withholding doses, and defines consensus criteria for safe administration and toxicity management. The somewhat heterogeneous best practices of 2014 will be compared and contrasted with the guidelines provided in 2001 and the package inserts from 1992 and 1998. Electronic supplementary material The online version of this article (doi:10.1186/s40425-014-0026-0) contains supplementary material, which is available to authorized users.en_US
dc.identifier.citationDutcher, J. P., Schwartzentruber, D. J., Kaufman, H. L., Agarwala, S. S., Tarhini, A. A., Lowder, J. N., & Atkins, M. B. (2014). High dose interleukin-2 (Aldesleukin)-expert consensus on best management practices-2014. Journal for ImmunoTherapy of Cancer, 2(1), 26.10.1186/s40425-014-0026-0en_US
dc.identifier.issn2051-1426en_US
dc.identifier.urihttps://hdl.handle.net/1805/22405
dc.language.isoen_USen_US
dc.publisherBMJen_US
dc.relation.isversionof10.1186/s40425-014-0026-0en_US
dc.relation.journalJournal for ImmunoTherapy of Canceren_US
dc.rightsAttribution 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.sourcePMCen_US
dc.subjectInterleukin-2en_US
dc.subjectClinical managementen_US
dc.subjectCytokinesen_US
dc.subjectRenal cell carcinomaen_US
dc.subjectMelanomaen_US
dc.subjectTreatment guidelinesen_US
dc.titleHigh dose interleukin-2 (Aldesleukin) - expert consensus on best management practices-2014en_US
dc.typeArticleen_US
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