Publication:
Contemporary rends in high-dose interleukin-2 use for metastatic renal cell carcinoma in the United States

dc.contributor.authorTİNAY, İLKER
dc.contributor.authorsAllard, Christopher B.; Gelpi-Hammerschmidt, Francisco; Harshman, Lauren C.; Choueiri, Toni K.; Faiena, Izak; Modi, Parth; Chung, Benjamin I.; Tinay, Ilker; Singer, Eric A.; Chang, Steven L.
dc.date.accessioned2022-03-14T11:11:23Z
dc.date.accessioned2026-01-11T18:43:16Z
dc.date.available2022-03-14T11:11:23Z
dc.date.issued2015-11
dc.description.abstractBackground: Targeted therapies (TTs) have revolutionized metastatic renal cell carcinoma (mRCC) treatment in the past decade, largely replacing immunotherapy including high-dose interleukin-2 (HD IL-2) therapy. We evaluated trends in HD IL-2 use for mRCC in the IT era. Methods: Our cohort comprised a weighted estimate of all patients undergoing HD IL-2 treatment for mRCC from 2004 to 2012 using the Premier Hospital Database. We assessed temporal trends in HD IL-2 use including patient. disease, and hospital characteristics stratified by era (pre-TT uptake: 2004-2006, uptake: 2007-2009, and post-TT uptake: 2010-2012) and fitted multivariable regression models to identify predictors of treatment toxicity and tolerability. Results: An estimated 2,351 patients received HD IL-2 therapy for mRCC in the United States from 2004 to 2012. The use decreased from 2004 to 2008. HD IL-2 therapy became increasingly centralized in teaching hospitals (24% of treatments in 2004 and 89.5% in 2012). Most patients who received HD IL-2 therapy were men, white, younger than 60 years, had lung metastases, and were otherwise healthy. Vasopressors, intensive care unit admission, and hemodialysis were necessary in 53.4%, 33.0%, and 7.1%, respectively. Factors associated with toxicities in multivariable analyses included being unmarried, male sex, and multiple metastatic sites. African Americans and patients with single-site metastases were less likely to receive multiple treatment cycles. Conclusions: HD IL-2 therapy is used infrequently for mRCC in the United States, and its application has diminished with the uptake of TT. Patients are being increasingly treated in teaching hospitals, suggesting a centralization of care and possible barriers to access. A recent slight increase in HD IL-2 therapy use likely reflects recognition of the inability of TT to effect a complete response. (C) 2015 Elsevier Inc. All rights reserved.
dc.identifier.doi10.1016/j.urolonc.2015.06.014
dc.identifier.eissn1873-2496
dc.identifier.issn1078-1439
dc.identifier.pubmed26210683
dc.identifier.urihttps://hdl.handle.net/11424/246011
dc.identifier.wosWOS:000364404400013
dc.language.isoeng
dc.publisherELSEVIER SCIENCE INC
dc.relation.ispartofUROLOGIC ONCOLOGY-SEMINARS AND ORIGINAL INVESTIGATIONS
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectHigh-dose interleukin-2
dc.subjectImmunotherapy
dc.subjectRenal cell carcinoma
dc.subjectKidney cancer
dc.subjectTherapy trends
dc.subjectToxicity
dc.subjectINTERFERON-ALPHA
dc.subjectDOUBLE-BLIND
dc.subjectCANCER
dc.subjectSTATISTICS
dc.subjectSURVIVAL
dc.subjectANTIBODY
dc.subjectMELANOMA
dc.subjectSAFETY
dc.titleContemporary rends in high-dose interleukin-2 use for metastatic renal cell carcinoma in the United States
dc.typearticle
dspace.entity.typePublication
oaire.citation.issue11
oaire.citation.titleUROLOGIC ONCOLOGY-SEMINARS AND ORIGINAL INVESTIGATIONS
oaire.citation.volume33

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