Daratumumab plus Bortezomib, Melphalan, and Prednisone for Untreated Myeloma

María‐Victoria Mateos(Instituto de Investigación Biomédica de Salamanca), Meletios Α. Dimopoulos(National and Kapodistrian University of Athens), Michèle Cavo(University of Bologna), Kenshi Suzuki(Japanese Red Cross Medical Center), Andrzej Jakubowiak(University of Chicago Medical Center), Stefan Knop, Chantal Doyen(CHU Dinant Godinne UCL Namur), Paulo Lúcio(Champalimaud Foundation), Zsolt Nagy(Semmelweis University), Polina Kaplan(Regional Clinical Hospital named after II Mechnikov), Luděk Pour(University Hospital Brno), Mark Cook(University Hospitals Birmingham NHS Foundation Trust), Sebastian Grosicki(Medical University of Silesia), Andre H Crepaldi(Instituto Tropical de Medicina Reprodutiva), Anna Marina Liberati(Azienda Ospedaliera S.Maria), Philip Campbell, Tatiana Shelekhova(Saratov Research Institute of Traumatology and Orthopedics), Sung‐Soo Yoon(Seoul National University), Genadi Iosava(MED Institute), Tomoaki Fujisaki(Matsuyama Red Cross Hospital), Mamta Garg(Leicester Royal Infirmary), Christopher Chiu(Janssen (United States)), Jianping Wang(Janssen (United States)), Robin Carson(Janssen (United States)), Wendy Crist(Janssen (United States)), William Deraedt(Janssen (Belgium)), Huong Nguyen(Janssen (United States)), Ming Qi(Janssen (United States)), Jesús F. San Miguel(Centro de Investigación Biomédica en Red de Cáncer)
New England Journal of Medicine
December 12, 2017
Cited by 979Open Access
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Abstract

BACKGROUND: The combination of bortezomib, melphalan, and prednisone is a standard treatment for patients with newly diagnosed multiple myeloma who are ineligible for autologous stem-cell transplantation. Daratumumab has shown efficacy in combination with standard-of-care regimens in patients with relapsed or refractory multiple myeloma. METHODS: In this phase 3 trial, we randomly assigned 706 patients with newly diagnosed multiple myeloma who were ineligible for stem-cell transplantation to receive nine cycles of bortezomib, melphalan, and prednisone either alone (control group) or with daratumumab (daratumumab group) until disease progression. The primary end point was progression-free survival. RESULTS: white cells), as compared with 6.2% of those in the control group (P<0.001). The most common adverse events of grade 3 or 4 were hematologic: neutropenia (in 39.9% of the patients in the daratumumab group and in 38.7% of those in the control group), thrombocytopenia (in 34.4% and 37.6%, respectively), and anemia (in 15.9% and 19.8%, respectively). The rate of grade 3 or 4 infections was 23.1% in the daratumumab group and 14.7% in the control group; the rate of treatment discontinuation due to infections was 0.9% and 1.4%, respectively. Daratumumab-associated infusion-related reactions occurred in 27.7% of the patients. CONCLUSIONS: Among patients with newly diagnosed multiple myeloma who were ineligible for stem-cell transplantation, daratumumab combined with bortezomib, melphalan, and prednisone resulted in a lower risk of disease progression or death than the same regimen without daratumumab. The daratumumab-containing regimen was associated with more grade 3 or 4 infections. (Funded by Janssen Research and Development; ALCYONE ClinicalTrials.gov number, NCT02195479 .).


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