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Carfilzomib, Lenalidomide, and Dexamethasone for Relapsed Multiple Myeloma

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15110%2F15%3A33151064" target="_blank" >RIV/61989592:15110/15:33151064 - isvavai.cz</a>

  • Alternative codes found

    RIV/61988987:17110/15:A1601FYC RIV/00216208:11150/15:10288628 RIV/00179906:_____/15:10288628 RIV/00064165:_____/15:10288628

  • Result on the web

    <a href="http://dx.doi.org/10.1056/NEJMoa1411321" target="_blank" >http://dx.doi.org/10.1056/NEJMoa1411321</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1056/NEJMoa1411321" target="_blank" >10.1056/NEJMoa1411321</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Carfilzomib, Lenalidomide, and Dexamethasone for Relapsed Multiple Myeloma

  • Original language description

    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-freesurvival. 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% C

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    FD - Oncology and haematology

  • OECD FORD branch

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2015

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    New England Journal of Medicine

  • ISSN

    0028-4793

  • e-ISSN

  • Volume of the periodical

    372

  • Issue of the periodical within the volume

    2

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    11

  • Pages from-to

    142-152

  • UT code for WoS article

  • EID of the result in the Scopus database