TY - JOUR
T1 - Carfilzomib, lenalidomide, and dexamethasone for relapsed multiple myeloma
AU - ASPIRE Investigators
AU - Stewart, A. Keith
AU - Rajkumar, S. Vincent
AU - Dimopoulos, Meletios A.
AU - Masszi, Tamas
AU - Špicka, Ivan
AU - Oriol, Albert
AU - Hajek, Roman
AU - Rosinol, Laura
AU - Siegel, David S.
AU - Mihaylov, Georgi G.
AU - Goranova-Marinova, Vesselina
AU - Rajnics, Peter
AU - Suvorov, Aleksandr
AU - Niesvizky, Ruben
AU - Jakubowiak, Andrzej J.
AU - San-Miguel, Jesus F.
AU - Ludwig, Heinz
AU - Wang, Michael
AU - Maisnar, Vladimir
AU - Minarik, Jiri
AU - Bensinger, William I.
AU - Mateos, Maria Victoria
AU - Ben-Yehuda, Dina
AU - Kukreti, Vishal
AU - Zojwalla, Naseem
AU - Tonda, Margaret E.
AU - Yang, Xinqun
AU - Xing, Biao
AU - Moreau, Philippe
AU - Palumbo, Antonio
N1 - Publisher Copyright:
Copyright © 2015 Massachusetts Medical Society. All rights reserved.
PY - 2015/1/8
Y1 - 2015/1/8
N2 - 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.)
AB - 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.)
UR - http://www.scopus.com/inward/record.url?scp=84920599743&partnerID=8YFLogxK
U2 - 10.1056/NEJMoa1411321
DO - 10.1056/NEJMoa1411321
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C2 - 25482145
AN - SCOPUS:84920599743
SN - 0028-4793
VL - 372
SP - 142
EP - 152
JO - New England Journal of Medicine
JF - New England Journal of Medicine
IS - 2
ER -