View the Recording from the Roundtable meeting here.
Programme
14:30-14:35 – Welcome and introductions
Roundtable Co-Chairs:
- Andreas Charalambous, President, European Cancer Organisation
- Patrycja Rzadkowska, Patient Advisory Committee Member, European Cancer Organisation; and Patient Advocate for Pancreatic Cancers Europe.
- Mark Lawler, ECO Board Member and Chair in Translational Cancer Genomics, Queen's University Belfast.
14:35-15:10 – Genomic Tumour Testing in Europe in 2023: The Current Landscape
Co-chaired by Mark Lawler, and Cecilia Schott, Vice-President, Global Head Precision Diagnostics, Novartis.
Including contributions from expert speakers:
- Nicola Normanno, Director of Cell Biology and Biotherapy Unit, Director of the Transnational Research Department, INT Fondazione Pascale, Naples.
- Rosa Giuliani, Consultant medical oncologist, Guy's and St Thomas' NHS Foundation Trust.
- Anne-Marie Baird, President of Lung Cancer Europe and Patient Advisory Committee Member.
The session will:
- Describe latest headline data about the extent of access to genomic tumour testing in Europe.
- Recap on previous ECO policy considerations on genomic tumour testing, including its 2021 Action Report ‘Put to the Test: Empowering Genomics to Improve Cancer Care and Patient Lives’.
- Give overview on EU level and other major initiatives to assist the uptake of genomic tumour testing.
- Provide patient perspective on the current and anticipated future status of genomic tumour testing access in Europe.
15:10-15:50 – Developing The Infrastructure for Delivering Genomic Tumour Testing: Where Are We Now and Where Do We Need To Be
Co-chaired by Patrycja Rzadkowska, and Achim Escherich, Global Technical Companion Diagnostics Lead, Market Access, Menarini Stemline.
Including contributions from expert speakers:
The session will:
- Review the present state of readiness of European health and cancer care systems to provide access to genomic tumour testing, with a particular focus to matters such as workforce and laboratory infrastructure.
- Articulate current and future needs including in respect to digital technology and the best investments.
15:50-16:25 – The Value of Genomic Tumour Testing
Co-chaired by Patrycja Rzadkowska, and Elizabeth Sheppard, Global Pricing & Market Access Director, Oncology Diagnostic AstraZeneca.
Including contributions from expert speakers:
- Thomas Hofmarcher, Research Director, Swedish Institute for Health Economics.
- Mark Lawler, ECO Board Member and Chair in Translational Cancer Genomics, Queen's University Belfast.
- Marco Marchetti, Responsible, National center for health technology assessment (HTA), Italian National Institute of Health
The session will:
- Investigate the current approaches to reimbursing genomic tumour testing in Europe.
- Provide an understanding of the cost-benefit analysis related to genomic tumour testing.
- Give the political and legislative context to genomic tumour testing access, including with reference to the implementation of the EU HTA regulation.
16:25-17:00 – Genomic Tumour Testing: Looking Into The Future
Co-chaired by Mark Lawler, and Olivia McDermid, Senior Manager Global Health Policy - HTA & Oncology, Amgen Zug.
Including contributions from expert speakers:
- Michele Calabro, Director, European Regional and Local Health Authorities (EUREGHA)
- Maeve Lowery, Professor of Translational Cancer Medicine at Trinity College Dublin and Consultant Medical Oncologist at St James Hospital
- Audrey Wolf, Associate Director Healthcare Systems and SMEs, European Federation of Pharmaceutical Industries and Associations (EFPIA)
The session will:
- Consider some of the political obstacles that remain to be overcome in respect to expanding access to genomic tumour testing, including, but not limited to: the application of the in vitro diagnostics regulation (IVDR) and new EU level pharmaceutical regulation.
- Prioritise political actions and recommendations stemming from the roundtable’s discussions.