Related Experiment Video
Updated: Feb 4, 2026

In Vitro Methods for Comparing Target Binding and CDC Induction Between Therapeutic Antibodies: Applications in Biosimilarity Analysis
Published on: May 4, 2017
Preparing for the incoming wave of biosimilars in oncology
Elena Wolff-Holz1, Juan Garcia Burgos2, Rosa Giuliani3
1Medicinal Policy Issues, Paul-Ehrlich-Institut, Federal Institute for Vaccines and Biomedicines, Langen, Germany.
Abstract:
With the imminent arrival of oncology biosimilars in the therapeutic paradigm, stakeholders including a clinician, specialist nurse, patient advocate, regulator and economist provide their perspective on optimising the uptake of these new agents in the treatment of cancer. A number of key messages emerge, based on the discussion that took place during a session of the European Society for Medical Oncology's Annual Congress, ESMO Madrid 2017. First, for successful integration of biosimilars into the global healthcare paradigm, informing and educating the full scope of stakeholders, including clinicians, nurses, pharmacists and patients, is primordial. Success is dependent on providing solid evidence and ensuring all voices are heard. Second, for oncology medicines, much can be learnt from the growing experience of approved biosimilars in other disease indications, with success stories for patients, their healthcare providers and healthcare budgets alike. Finally, effective sustainability of the impact on healthcare budgets and the redirection of these savings require education and transparency.
Insights
Oncology biosimilars require stakeholder education for successful integration. Learning from other biosimilar successes and ensuring transparency in budget impacts are key to optimizing their use in cancer treatment.
Area of Science:
- Oncology
- Pharmacoeconomics
- Healthcare Policy
Background:
- The introduction of oncology biosimilars presents new opportunities and challenges in cancer care.
- Stakeholder perspectives are crucial for understanding and optimizing the adoption of these novel therapeutic agents.
Purpose of the Study:
- To gather and synthesize perspectives from diverse stakeholders on optimizing the uptake of oncology biosimilars.
- To identify key strategies for the successful integration of biosimilars into cancer treatment paradigms.
Main Methods:
- A discussion session involving clinicians, specialist nurses, patient advocates, regulators, and economists at the European Society for Medical Oncology (ESMO) Annual Congress 2017.
- Qualitative synthesis of key messages emerging from stakeholder discussions.
Main Results:
- Successful integration necessitates comprehensive education for all stakeholders, including healthcare professionals and patients.
- Evidence-based decision-making and incorporating diverse voices are critical for biosimilar adoption.
- Experience with biosimilars in other therapeutic areas offers valuable insights for oncology.
- Sustainability of healthcare budget impacts and savings requires transparency and ongoing education.
Conclusions:
- Optimizing oncology biosimilar uptake requires a multi-faceted approach centered on education, evidence, and inclusivity.
- Leveraging existing biosimilar experience and ensuring financial transparency are vital for long-term success.
More Related Videos
Related Concept Videos
Drug Products: Biologics, Biosimilars and Interchangeables
The Wave Nature of Light
Wave Parameters
Reflection of Waves
Half wave rectifier
Full wave rectifier

