Efficacy of everolimus in advanced renal cell carcinoma: a double-blind, randomised, placebo-controlled phase III trial Journal Article


Authors: Motzer, R. J.; Escudier, B.; Oudard, S.; Hutson, T. E.; Porta, C.; Bracarda, S.; Grünwald, V.; Thompson, J. A.; Figlin, R. A.; Hollaender, N.; Urbanowitz, G.; Berg, W. J.; Kay, A.; Lebwohl, D.; Ravaud, A.
Article Title: Efficacy of everolimus in advanced renal cell carcinoma: a double-blind, randomised, placebo-controlled phase III trial
Abstract: Background: Everolimus (RAD001) is an orally administered inhibitor of the mammalian target of rapamycin (mTOR), a therapeutic target for metastatic renal cell carcinoma. We did a phase III, randomised, double-blind, placebo-controlled trial of everolimus in patients with metastatic renal cell carcinoma whose disease had progressed on vascular endothelial growth factor-targeted therapy. Methods: Patients with metastatic renal cell carcinoma which had progressed on sunitinib, sorafenib, or both, were randomly assigned in a two to one ratio to receive everolimus 10 mg once daily (n=272) or placebo (n=138), in conjunction with best supportive care. Randomisation was done centrally via an interactive voice response system using a validated computer system, and was stratified by Memorial Sloan-Kettering Cancer Center prognostic score and previous anticancer therapy, with a permuted block size of six. The primary endpoint was progression-free survival, assessed via a blinded, independent central review. The study was designed to be terminated after 290 events of progression. Analysis was by intention to treat. This study is registered with ClinicalTrials.gov, number NCT00410124. Findings: All randomised patients were included in efficacy analyses. The results of the second interim analysis indicated a significant difference in efficacy between arms and the trial was thus halted early after 191 progression events had been observed (101 [37%] events in the everolimus group, 90 [65%] in the placebo group; hazard ratio 0·30, 95% CI 0·22-0·40, p<0·0001; median progression-free survival 4·0 [95% CI 3·7-5·5] vs 1·9 [1·8-1·9] months). Stomatitis (107 [40%] patients in the everolimus group vs 11 [8%] in the placebo group), rash (66 [25%] vs six [4%]), and fatigue (53 [20%] vs 22 [16%]) were the most commonly reported adverse events, but were mostly mild or moderate in severity. Pneumonitis (any grade) was detected in 22 (8%) patients in the everolimus group, of whom eight had pneumonitis of grade 3 severity. Interpretation: Treatment with everolimus prolongs progression-free survival relative to placebo in patients with metastatic renal cell carcinoma that had progressed on other targeted therapies. Funding: Novartis Oncology. © 2008 Elsevier Ltd. All rights reserved.
Keywords: vasculotropin; adult; cancer survival; controlled study; treatment outcome; aged; aged, 80 and over; disease-free survival; middle aged; major clinical study; clinical trial; fatigue; neutropenia; sorafenib; bevacizumab; interferon; placebo; sunitinib; advanced cancer; cancer growth; diarrhea; drug dose reduction; drug efficacy; drug safety; drug withdrawal; hypophosphatemia; side effect; treatment duration; alpha interferon; anorexia; cancer palliative therapy; interleukin 2; metastasis; quality of life; controlled clinical trial; infection; anemia; protein targeting; leukopenia; lung disease; mucosa inflammation; nausea; randomized controlled trial; stomatitis; thrombocytopenia; vomiting; kidney carcinoma; kidney neoplasms; temsirolimus; asthenia; coughing; dyspnea; hyperglycemia; lymphocytopenia; pneumonia; rash; karnofsky performance status; carcinoma, renal cell; multicenter study; scoring system; neoplasm metastasis; hazard ratio; phase 3 clinical trial; hypercholesterolemia; randomization; crossover procedure; double blind procedure; double-blind method; dry skin; everolimus; sirolimus; immunosuppressive agents; hypertriglyceridemia; hypocalcemia; computer system; interactive voice response system
Journal Title: Lancet
Volume: 372
Issue: 9637
ISSN: 0140-6736
Publisher: Elsevier Science, Inc.  
Date Published: 2008-08-09
Start Page: 449
End Page: 456
Language: English
DOI: 10.1016/s0140-6736(08)61039-9
PUBMED: 18653228
PROVIDER: scopus
DOI/URL:
Notes: --- - "Cited By (since 1996): 615" - "Export Date: 17 November 2011" - "CODEN: LANCA" - "Source: Scopus"
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  1. Robert Motzer
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