To Earn CE for this Session: Watch the on-demand recording in its entirety, thenclick here to complete the CE quiz for this session.
Oncology
G. Sylvester Price, DVM, DACVIM (SAIM & Oncology)
Head of Non-Infectious Disease Research
Boehringer Ingelheim
Duluth, Georgia, United States
Christopher Loss, DVM (he/him/his)
Veterinary Medical Officer
FDA / Center for Veterinary Medicine
Alexandria, Virginia, United States
Douglas H. Thamm, VMD, DACVIM (Oncology)
Barbara Cox Anthony Professor of Oncology
Colorado State University
Fort Collins, Colorado, United States
Recent advances in molecular diagnostic tests that provide insight into genetic mutations of a patient's tumor have the potential to improve clinical outcomes. However, there are multiple pharmacologic, pharmaceutical, and clinical pathology factors that may hinder the successful clinical application of this precision medicine approach. This panel is a Part II follow-up to Part I presentation on this topic; the panelist and audience will exchange ideas the importance of these when selecting a therapeutic based upon molecular diagnostic test.