Aditya Bardia, MD, MPH, is joined by Adam Brufsky, MD, PhD, Sara Hurvitz, MD, and Hope Rugo, MD, for a discussion on recent FDA approvals, guidance on therapeutic sequencing, and the future of HER2+ breast cancer.
The panel reviews some of the newest players in the HER2+ breast cancer treatment landscape and discusses how to incorporate these agents into a patient’s treatment plan.
Dr. Bardia has disclosed that he has conculted for Biotheranostics; Daiichi Sankyo; AstraZeneca; Genentech; Immunomedics; Eli Lilly and Company; Novartis; Pfizer; Puma Biotechnology; Merck; Philips; Radius Health; Sanofi; Spectrum Pharmaceuticals; Foundation Medicine; Taiho Pharmaceutical
Dr. Hurvitz has previously received research grants from: Ambrx; Amgen Inc.; Bayer HealthCare Pharmaceuticals; Daiichi Sankyo, Inc.; Dignitana AB; Eli Lilly and Company; Genentech, Inc.; GlaxoSmithKline; Immunomedics; MacroGenics, Inc.; Novartis Pharmaceuticals Corporation; OBI Pharma, Inc.; Pfizer Inc; Pieris Pharmaceuticals Inc; Puma Biotechnology; Radius Health; Roche Pharma; sanofi-aventis; Seattle Genetics, Inc.
Dr. Brufsky has disclosed no relevant financial relationships
Dr. Rugo has been a consultant for Samsung and Puma; and has received research grants from: Pfizer; Merck; Novartis; Eli Lilly and Company; Genentech; OBI; Odonate; Daiichi Sankyo; Seattle Genetics; Eisai; MacroGenics; Sermonix; Immunomedics