Vienna, Austria

ESTRO 2025

Local time in host city

Programme

4 Sessions
Saturday
May 03
08:45 - 10:00
Lehar 1-3
Edmond Sterpin, Belgium;
Vlad Badiu, The Netherlands
In particle therapy, accurately determining where particles stop in the patient is crucial to ensure safer and more precise treatments. Over the past decade, various technological solutions have been proposed, but no industrial system for large-scale in vivo treatment verification is currently available. Prof. Katia Parodi will present an overview of these solutions, while Prof. Christian Richter will discuss existing clinical data, emphasizing the real-world impact and importance of integrating verification into clinical workflows. Prof. Thomas Bortfeld will highlight how verification could enable innovative treatment techniques. Dr. Julien Smeets will conclude by addressing the technical and industrial challenges of integrating these systems into complex and evolving particle therapy platforms, including considerations for proton arc therapy and FLASH.
Symposium
Physics
Dosimetry & QA
Saturday
May 03
12:55 - 13:25
Business 3-4
Meet & Greet sessions provide journey participants with the opportunity to network and to meet ESTRO focus group representatives who developed these journeys. Registration for Meet & Greet sessions is required via the Journeys tab on the ESTRO 2025 website.
Meet & Greet
Dosimetry & QA
Saturday
May 03
17:00 - 18:00
Lehar 1-3
Sarah Kelly, Belgium;
Stephen Kry, USA
Proffered Papers are presented in one of the sessions scheduled in the main session halls. Each author will present orally for 7 minutes, followed by 3 minutes for discussion. Sessions will be recorded and available on-demand.
Proffered Papers
Physics
Dosimetry & QA
Sunday
May 04
08:45 - 10:00
Mahler
Corinne Faivre-Finn, United Kingdom;
Joost Verhoeff, The Netherlands
This session explores innovative approaches to clinical research in radiation oncology, challenging traditional methodologies and highlighting the need for adaptability in a rapidly evolving field. The first talk discusses the limitations of RCTs, including their high costs, long timelines, and challenges in keeping pace with technological advancements. The second talk examines the role of real-world evidence, defining its scope, regulatory perspectives, and impact on clinical decision-making. The third talk explores pragmatic trials as a bridge between efficacy and real-world effectiveness, addressing their design and implementation. Finally, the session covers the Trials Within Cohort (TwiCs) approach, demonstrating how cohort-based randomised trials can offer ethical and practical advantages. Together, these talks offer a roadmap for modernizing clinical research in radiation oncology.
Symposium
Interdisciplinary
Dosimetry & QA / GI / Lung / Soft Tissue
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