@article {7500,
	title = {Carfilzomib, lenalidomide, and dexamethasone for relapsed multiple myeloma},
	journal = {New England Journal of Medicine},
	volume = {372},
	year = {2015},
	note = {Cited By :175Export Date: 21 February 2017},
	month = {2015},
	pages = {142 - 152},
	abstract = {Background Lenalidomide plus dexamethasone is a reference treatment for relapsed multiple myeloma. The combination of the proteasome inhibitor carfilzomib with lenalidomide and dexamethasone has shown efficacy in a phase 1 and 2 study in relapsed multiple myeloma. Methods We randomly assigned 792 patients with relapsed multiple myeloma to carfilzomib with lenalidomide and dexamethasone (carfilzomib group) or lenalidomide and dexamethasone alone (control group). The primary end point was progression-free survival. Results Progression-free survival was significantly improved with carfilzomib (median, 26.3 months, vs. 17.6 months in the control group; hazard ratio for progression or death, 0.69; 95\% confidence interval [CI], 0.57 to 0.83; P = 0.0001). The median overall survival was not reached in either group at the interim analysis. The Kaplan-Meier 24-month overall survival rates were 73.3\% and 65.0\% in the carfilzomib and control groups, respectively (hazard ratio for death, 0.79; 95\% CI, 0.63 to 0.99; P = 0.04). The rates of overall response (partial response or better) were 87.1\% and 66.7\% in the carfilzomib and control groups, respectively (P<0.001; 31.8\% and 9.3\% of patients in the respective groups had a complete response or better; 14.1\% and 4.3\% had a stringent complete response). Adverse events of grade 3 or higher were reported in 83.7\% and 80.7\% of patients in the carfilzomib and control groups, respectively; 15.3\% and 17.7\% of patients discontinued treatment owing to adverse events. Patients in the carfilzomib group reported superior health-related quality of life. Conclusions In patients with relapsed multiple myeloma, the addition of carfilzomib to lenalidomide and dexamethasone resulted in significantly improved progression-free survival at the interim analysis and had a favorable risk-benefit profile. (Funded by Onyx Pharmaceuticals; ClinicalTrials.gov number, NCT01080391.) Copyright {\textcopyright} 2015 Massachusetts Medical Society. All rights reserved.},
	url = {https://www.scopus.com/inward/record.uri?eid=2-s2.0-84920599743\&doi=10.1056\%2fNEJMoa1411321\&partnerID=40\&md5=48928baffa77798bbe1ff41b1665a84f},
	author = {Stewart, A.K. and Rajkumar, S.V. and Dimopoulos, M.A. and Masszi, T. and {\v S}picka, I. and Oriol, A. and Hajek, R. and Rosinol, L. and Siegel, D.S. and Mihaylov, G.G. and Goranova-Marinova, V. and Rajnics, P. and Suvorov, A. and Niesvizky, R. and Jakubowiak, A.J. and San-Miguel, J.F. and Ludwig, H. and Wang, M. and Maisnar, V. and Minarik, J. and Bensinger, W.I. and Mateos, M.-V. and Ben-Yehuda, D. and Kukreti, V. and Zojwalla, N. and Tonda, M.E. and Yang, X. and Xing, B. and Moreau, P. and Palumbo, A.}
}
