Bridio Sara, Deceuninck Pierre, Whelan Maurice, Worth Andrew
European Commission, Joint Research Centre, Ispra, Italy.
Sci Prog. 2025 Jul-Sep;108(3):368504251344145. doi: 10.1177/00368504251344145. Epub 2025 Sep 1.
Computational medicine promises significant advancements in healthcare, using physics-based simulations and artificial intelligence to optimise disease diagnosis, personalise treatment strategies and accelerate medical innovation. Biomedical research efforts are generating a growing number of computational models of human pathophysiology and medical treatments, with advanced applications in areas such as cardiovascular diseases, orthopaedics and cancer diagnosis. However, the widespread adoption of these models is hindered by technological and regulatory barriers. This article provides an overview of the potential impact, needs and challenges of the adoption of in silico medicine in the healthcare ecosystem, with a focus on initiatives to sustain this technology within the European Union's regulatory environment. The article introduces the concept of the 'computational model lifecycle' as a framework to describe the stages from academic research to pre-clinical and clinical applications, analysing key opportunities and challenges in translating these technologies at each stage. These challenges are associated with data management, standards for model credibility assessment, transparency of regulatory frameworks, and clinical integration. The article highlights European initiatives such as the European Health Data Space and the Virtual Human Twins Initiative, aimed at fostering the development and application of computational medicine in healthcare.
计算医学有望推动医疗保健领域取得重大进展,它利用基于物理的模拟和人工智能来优化疾病诊断、个性化治疗策略并加速医学创新。生物医学研究正在生成越来越多的人体病理生理学和医学治疗的计算模型,并在心血管疾病、骨科和癌症诊断等领域得到了广泛应用。然而,这些模型的广泛应用受到技术和监管障碍的阻碍。本文概述了在医疗保健生态系统中采用虚拟医学的潜在影响、需求和挑战,重点关注在欧盟监管环境下维持这项技术的举措。文章引入了“计算模型生命周期”的概念,作为描述从学术研究到临床前和临床应用各个阶段的框架,分析了在每个阶段转化这些技术的关键机遇和挑战。这些挑战与数据管理、模型可信度评估标准、监管框架的透明度以及临床整合有关。文章强调了欧洲的一些举措,如欧洲健康数据空间和虚拟人类双胞胎计划,旨在促进计算医学在医疗保健中的开发和应用。