Evaluating the Role of Biosimilars in Oncology: Implications for Clinical Pharmacists
A CE Midday Symposium Conducted at the 52nd ASHP Midyear Clinical Meeting and Exhibition
Wednesday, December 6, 2017
Orange County Convention Center
Archived, for viewing purposes only.
In oncology, biosimilar versions of major anticancer therapies and supportive care agents are emerging. Clinically, their introduction may increase the number of patients accessing biologic therapies and, if appropriate, permit access to these therapies at earlier stages of disease.
However, clinicians face challenges with these new therapeutic entities, including understanding the immunogenicity, interchangeability, and substitutions related to biosimilars. Further, concerns over biosimilars may focus on the unknown safety issues surrounding the inevitable differences that exist between a biosimilar and its reference product, and also appropriate naming conventions used to distinguish biosimilar drugs. Similarly, extrapolation across indications, interchangeability, and automatic substitution are not yet universally understood. Additionally, differing biologic formulations may pose concerns for efficacy and safety due to changes in manufacturing processes, protocols, packaging, and cold storage delivery. This CE Midday Symposium features an expert faculty presenting insights and experience to guide pharmacists through the challenges and opportunities of an emerging era of biosimilars in oncology.