ASH Clinical News February 2017 New | Page 34

On Location ASH Annual Meeting Double Hematopoietic Cell Transplantation Extends Progression-Free Survival Over Single Transplant in Myeloma Patients Following bortezomib-based induction therapy, patients with newly diagnosed multiple PAGE 6 myeloma (MM) who received double autologous hematopoietic cell transplantation (AHCT) had longer progression-free survival (PFS) than patients who received a single AHCT, according to pre- liminary results from a phase III study by the European Myeloma Network. The benefit appeared to be greatest for patients who had disease-related factors asso- ciated with poor prognosis, the researchers added. “In the age of novel thera- pies for MM, the role of single versus double AHCT needs to be prospectively investigated,” lead KOVALTRY ® TAKING THE NEXT STEP—TOGETHER Recommended prophylaxis dose Regimen Children aged ≤ 12 years 1 25-50 IU/kg 2x/week, 3x/week, or EOD Adolescents and adults 1 20-40 IU/kg 2x/week or 3x/week Bayer Access Solutions If your patient’s insurance does not cover KOVALTRY ® , we may be able to provide KOVALTRY ® to your patient at no cost for up to one year while insurance issues are being resolved* Call 1-800-288-8374 from 8:00 AM -8:00 PM (ET) Monday-Friday to connect with a Case Specialist. Spanish-speaking Case Specialists are also available *Some restrictions apply. Please call 1-800-288-8374 to learn more. SELECTED IMPORTANT SAFETY INFORMATION KOVALTRY ® is contraindicated in patients who have a history of hypersensitivity reactions to the active substance, to any of the excipients, or to mouse or hamster proteins. Hypersensitivity reactions, including anaphylaxis, are possible with KOVALTRY ® . Early signs of hypersensitivity reactions, which can progress to anaphylaxis, may include chest or throat tightness, dizziness, mild hypotension and nausea. Discontinue KOVALTRY ® if symptoms occur and seek immediate emergency treatment. For additional important risk and use information, please see Brief Summary on following pages. You are encouraged to report negative side effects or quality complaints of prescription drugs to the FDA. Visit www.fda.gov/medwatch or call 1-800-FDA-1088. References: 1. KOVALTRY ® [prescribing information]. Whippany, NJ: Bayer HealthCare LLC; 2016. 2. Data on fi le. Bayer HealthCare Pharmaceuticals, Inc; 2016. 3. Ljung R, Kenet G, Mancuso ME, et al. BAY 81-8973 safety and effi cacy for prophylaxis and treatment of bleeds in previously treated children with severe hemophilia A: results of the LEOPOLD Kids Trial [published online December 9, 2015]. Haemophilia. doi:10.1111/hae.12866. Bayer, the Bayer Cross, and KOVALTRY are registered trademarks of Bayer. © 2016 Bayer. All rights reserved. Printed in USA 05/16 PP-675-US-0202 T:1 S: