Christopher B Allard1, Francisco Gelpi-Hammerschmidt2, Lauren C Harshman3, Toni K Choueiri3, Izak Faiena4, Parth Modi4, Benjamin I Chung5, Ilker Tinay6, Eric A Singer4, Steven L Chang7. 1. Division of Urology, Brigham and Women׳s Hospital, Harvard Medical School, Boston, MA; Department of Urology, Massachusetts General Hospital, Boston, MA. Electronic address: Callard@mgh.harvard.edu. 2. Division of Urology, Brigham and Women׳s Hospital, Harvard Medical School, Boston, MA; Department of Urology, Massachusetts General Hospital, Boston, MA. 3. Kidney Cancer Center, Dana-Farber Cancer Institute, Brigham and Women׳s Hospital, Harvard Medical School, Boston, MA. 4. Section of Urologic Oncology, Rutgers Institute of New Jersey and Robert Wood Johnson Medical School, New Brunswick, NJ. 5. Department of Urology, Stanford School of Medicine, Palo Alto, CA. 6. Division of Urology, Brigham and Women׳s Hospital, Harvard Medical School, Boston, MA; Department of Urology, Marmara University School of Medicine, Istanbul, Turkey. 7. Division of Urology, Brigham and Women׳s Hospital, Harvard Medical School, Boston, MA.
Abstract
BACKGROUND: 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 TT 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.
BACKGROUND: Targeted therapies (TTs) have revolutionized metastatic renal cell carcinoma (mRCC) treatment in the past decade, largely replacing immunotherapy including high-dose interleukin-2 (HDIL-2) therapy. We evaluated trends in HDIL-2 use for mRCC in the TT era. METHODS: Our cohort comprised a weighted estimate of all patients undergoing HDIL-2 treatment for mRCC from 2004 to 2012 using the Premier Hospital Database. We assessed temporal trends in HDIL-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 HDIL-2 therapy for mRCC in the United States from 2004 to 2012. The use decreased from 2004 to 2008. HDIL-2 therapy became increasingly centralized in teaching hospitals (24% of treatments in 2004 and 89.5% in 2012). Most patients who received HDIL-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:HDIL-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 HDIL-2 therapy use likely reflects recognition of the inability of TT to effect a complete response.
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