Head, Oncology Deparment Bon Animal Medical Center Suwon, Kyonggi-do, Republic of Korea
Presentation Description / Summary: Targeted therapies have reshaped veterinary oncology since the introduction of toceranib; however, their clinical application has often remained empiric rather than truly individualized. This session explores the transition from traditional, generalized use of tyrosine kinase inhibitors (TKIs) toward a precision oncology framework, emphasizing how molecular and protein-level biomarkers can support more rational, patient-specific treatment decisions. The lecture will begin with a clinically oriented overview of commonly used TKIs—including sorafenib, lapatinib, and trametinib—focusing on their therapeutic positioning, key signaling pathways, and characteristic, drug-specific toxicity profiles relevant to clinical practice. Through case-based examples, attendees will learn how DNA mutation profiling and immunohistochemical (IHC) protein expression are integrated in daily clinical practice to guide targeted therapy selection in dogs and cats with a range of solid tumors. These cases will highlight the complementary roles of genetic and protein-level data in precision treatment planning. Finally, emerging integrative strategies—including the combined use of genetic mutation profiling and 3D organoid-based drug sensitivity testing—will be discussed as evolving tools that may further refine personalized therapeutic decision-making in advanced-stage tumors. This lecture translates molecular and biomarker research into practical guidance for daily clinical oncology, providing a framework for biomarker-guided use of targeted therapies and illustrating how precision oncology can meaningfully improve therapeutic decision-making and clinical outcomes in small-animal oncology.
Learning Objectives:
Upon completion, participants will be able to describe the evolution of targeted therapies in small-animal oncology and explain the rationale for transitioning from empiric TKI use to a precision oncology framework.
Upon completion, participants will be able to compare the clinical roles, target pathways, and characteristic toxicity profiles of commonly used TKIs, including sorafenib, lapatinib, and trametinib.
Upon completion, participants will be able to apply DNA mutation profiling and immunohistochemical (IHC) protein expression data to guide targeted therapy selection in dogs and cats with solid tumors.
Upon completion, participants will be able to discuss the emerging role of integrated approaches, including genetic profiling and 3D organoid-based drug sensitivity testing, in personalized therapeutic decision-making for advanced-stage tumors.