Elotuzumab plus lenalidomide/dexamethasone for relapsed or refractory multiple myeloma: ELOQUENT-2 follow-up and post-hoc analyses on progression-free survival and tumour growth

. 2017 Sep ; 178 (6) : 896-905. [epub] 20170705

Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic

Typ dokumentu klinické zkoušky, fáze III, časopisecké články, randomizované kontrolované studie

Perzistentní odkaz   https://www.medvik.cz/link/pmid28677826

The randomized phase III ELOQUENT-2 study (NCT01239797) evaluated the efficacy and safety of elotuzumab + lenalidomide/dexamethasone (ELd) versus lenalidomide/dexamethasone (Ld) in relapsed/refractory multiple myeloma. ELd reduced the risk of disease progression/death by 30% versus Ld (hazard ratio [HR] 0·70). Median time from diagnosis was 3·5 years. We present extended 3-year follow-up data. Endpoints included progression-free survival (PFS), overall response rate (ORR) and interim overall survival (OS). Exploratory post-hoc analyses included impact of time from diagnosis and prior lines of therapy on PFS, and serum M-protein dynamic modelling. ORR was 79% (ELd) and 66% (Ld) (P = 0·0002). ELd reduced the risk of disease progression/death by 27% versus Ld (HR 0·73; P = 0·0014). Interim OS demonstrated a trend in favour of ELd (P = 0·0257); 1-, 2- and 3-year rates with ELd versus Ld were: 91% versus 83%, 73% versus 69% and 60% versus 53%. In patients with ≥ median time from diagnosis and one prior therapy, ELd resulted in a 53% reduction in the risk of progression/death versus Ld (HR 0·47). Serum M-protein dynamic modelling showed slower tumour regrowth with ELd. Adverse events were comparable between arms. ELd provided a durable and clinically relevant improvement in efficacy, with minimal incremental toxicity.

1st Department of Medicine Department of Haematology 1st Faculty of Medicine Charles University and General Teaching Hospital Prague Prague Czech Republic

AbbVie Biotherapeutics Inc Redwood City CA USA

Clinica Universidad de Navarra Investigación Médica Aplicada IDISNA CIBERONC Pamplona Spain

Clinical Pharmacology and Pharmacometrics Bristol Myers Squibb Lawrenceville NJ USA

Davidoff Cancer Center Rabin Medical Center Petah Tikva Israel

Department of Cancer Prevention Medical University of Silesia Katowice Poland

Department of Clinical Therapeutics National and Kapodistrian University of Athens School of Medicine Athens Greece

Department of Haemato oncology and Bone Marrow Transplantation Medical University of Lublin Lublin Poland

Department of Haematology Ankara University Ankara Turkey

Department of Haematology University Hospital Nantes France

Department of Hematology and Medical Oncology Winship Cancer Institute Emory University School of Medicine Atlanta GA USA

Department of Medical Oncology and Haematology Princess Margaret Cancer Centre Toronto ON Canada

Department of Medical Oncology Dana Farber Cancer Institute Boston MA USA

Department of Oncology Cross Cancer Institute and University of Alberta Edmonton AB Canada

Division of Hematologic Oncology Dana Farber Cancer Institute Boston MA USA

Division of Hematology Queen Elizabeth 2 Health Sciences Centre and Dalhousie University Halifax NS Canada

Global Biometric Sciences Bristol Myers Squibb Lawrenceville NJ USA

Global Biostatistics Bristol Myers Squibb Lawrenceville NJ USA

Global Clinical Research Bristol Myers Squibb Lawrenceville NJ USA

Haematology Department University Hospital of Salamanca Instituto de Investigación Biomédica de Salamanca Salamanca Spain

Institute of Haematology Assuta Medical Centers Tel Aviv Israel

Myeloma Unit Division of Haematology University of Torino Azienda Ospedaliero Universitaria Città della Salute e della Scienza di Torino Torino Italy

Oncology Clinical Development Bristol Myers Squibb Lawrenceville NJ USA

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