| Literature DB >> 24833354 |
Jesús San-Miguel1, Joan Bladé2, Ofer Shpilberg3, Sebastian Grosicki4, Frédéric Maloisel5, Chang-Ki Min6, Marta Polo Zarzuela7, Tadeusz Robak8, Sripada V S S Prasad9, Yeow Tee Goh10, Jacob Laubach11, Andrew Spencer12, María-Victoria Mateos13, Antonio Palumbo14, Tom Puchalski15, Manjula Reddy15, Clarissa Uhlar15, Xiang Qin15, Helgi van de Velde16, Hong Xie15, Robert Z Orlowski17.
Abstract
Because interleukin-6 (IL-6) is considered important in the proliferation of early multiple myeloma (MM), we hypothesized that the addition of the anti-IL-6 monoclonal antibody siltuximab to the bortezomib-melphalan-prednisone (VMP) regimen would improve outcomes in transplant-ineligible patients with newly diagnosed MM. One hundred and six patients were randomized to receive 9 cycles of VMP or VMP plus siltuximab (11 mg/kg every 3 weeks) followed by siltuximab maintenance. Baseline characteristics were well balanced except for immunoglobulin A subtype and 17p deletions. With a complete response (CR) rate of 27% on siltuximab plus VMP (S+VMP) and 22% on VMP, the study did not confirm its hypothesis that the addition of siltuximab would increase the CR rate by at least 10%. Overall response rate was 88% on S+VMP and 80% on VMP, and at least very good partial response rates were 71% and 51% (P = .0382), respectively. Median progression-free survival (17 months) and 1-year overall survival (88%) were identical in the 2 arms. Grade ≥3 adverse-event incidence was 92% on S+VMP and 81% on VMP (P = .09), with trends toward more hematologic events and infections on S+VMP. Maintenance therapy with siltuximab was well tolerated. In conclusion, the addition of siltuximab to VMP did not improve the CR rate or long-term outcomes. This study was registered at http://clinicaltrials.gov as #NCT00911859.Entities:
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Year: 2014 PMID: 24833354 PMCID: PMC4123433 DOI: 10.1182/blood-2013-12-546374
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113