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dc.contributor.author Stewart AK
dc.contributor.author Rajkumar SV
dc.contributor.author Dimopoulos MA
dc.contributor.author Masszi, Tamás
dc.contributor.author Spicka I
dc.contributor.author Oriol A
dc.contributor.author Hajek R
dc.contributor.author Rosinol L
dc.contributor.author Siegel DS
dc.contributor.author Mihaylov GG
dc.contributor.author Goranova-Marinova V
dc.contributor.author Rajnics P
dc.contributor.author Suvorov A
dc.contributor.author Niesvizky R
dc.contributor.author Jakubowiak AJ
dc.contributor.author San-Miguel JF
dc.contributor.author Ludwig H
dc.contributor.author Wang M
dc.contributor.author Maisnar V
dc.contributor.author Minarik J
dc.contributor.author Bensinger WI
dc.contributor.author Mateos MV
dc.contributor.author Ben-Yehuda D
dc.contributor.author Kukreti V
dc.contributor.author Zojwalla N
dc.contributor.author Tonda ME
dc.contributor.author Yang X
dc.contributor.author Xing B
dc.contributor.author Moreau P
dc.contributor.author Palumbo A
dc.contributor.author the ASPIRE Investigators
dc.date.accessioned 2015-09-09T07:13:55Z
dc.date.available 2015-09-09T07:13:55Z
dc.date.issued 2014
dc.identifier 84920599743
dc.identifier.citation pagination=142-152; journalVolume=372; journalIssueNumber=2; journalTitle=NEW ENGLAND JOURNAL OF MEDICINE;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/2060
dc.identifier.uri doi:10.1056/NEJMoa1411321
dc.description.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 .).
dc.relation.ispartof urn:issn:0028-4793
dc.title Carfilzomib, Lenalidomide, and Dexamethasone for Relapsed Multiple Myeloma.
dc.type Journal Article
dc.date.updated 2015-07-28T11:10:06Z
dc.language.rfc3066 en
dc.identifier.mtmt 2794257
dc.identifier.wos 000347443300009
dc.identifier.pubmed 25482145
dc.contributor.department SE/AOK/K/III. Sz. Belgyógyászati Klinika
dc.contributor.institution Semmelweis Egyetem
dc.mtmt.swordnote ASPIRE Investigators.


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