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Immunotherapy for Renal Cell Carcinoma

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Disclaimer This Guideline a empts to define principles of prac ce that should produce high-quality pa ent care. It is applicable to specialists, primary care providers and ancillary healthcare providers. This Guideline should not be considered exclusive of other methods of care reasonably directed at obtaining the same results. The ul mate judgment concerning the propriety of any course of conduct must be made by the clinician a er considera on of each individual pa ent situa on. Neither IGC, SITC, nor the authors endorse any product or service associated with the distributor of this clinical reference tool. Abbrevia ons CNS, central nervous system; DFS, disease-free survival; ECOG, Eastern Coopera ve Oncology Group; HD, high dose; HQ, hydroxychloroquine; IFN, interferon; IL, interleukin; mRCC, metasta c RCC; OS, overall survival; PD, programmed death; PFS, progression-free survival; PS, performance status; RCC, renal cell carcinoma; RFS, recurrence-free survival; RT, radia on therapy; SD, stable disease; SBRT, stereotac c body radia on therapy; S/P, status post; TKI, tyrosine kinase inhibitor; VEGF, vascular endothelial growth factor Source Rini BI, McDermo DF, Hammers H, Bro W, Bukowski RM, Faba B, Faba J, Figlin RA, Hutson T, Jonasch E, Joseph RW, Leibovich BC, Olencki T, Pantuck AJ, Quinn DI, Seery V, Voss MH, Wood CG, Wood LS, Atkins MB. Society for Immunotherapy of Cancer consensus statement on immunotherapy for the treatment of renal cell carcinoma. J Immunother Cancer. 2016 Nov 15;4:81. jitc.biomedcentral.com. 106 Commerce Street, Suite 105 Lake Mary, FL 32746 TEL: 407.878.7606 • FAX: 407.878.7611 For additional copies, order at GuidelineCentral.com Copyright © 2017 All rights reserved SITCRCC17053e Defini on of Evidence Grades Level Defini on A Strong suppor ng evidence-based data from prospec ve, randomized, controlled trials, meta-analyses, long-term follow-up of prospec ve, uncontrolled trials (HD IL-2 only) B Moderate suppor ng data from uncontrolled, prospec ve clinical trials C Weak suppor ng data from retrospec ve reviews and case reports Percentages Propor on of Task Force members favoring recommenda on

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