Stamatakos Georgios, Kolokotroni Eleni, Panagiotidou Foteini, Tsampa Stamatia, Kyroudis Christos, Spohn Simon, Grosu Anca-Ligia, Baltas Dimos, Zamboglou Constantinos, Sachpazidis Ilias
In silico Oncology and In silico Medicine Group, Institute of Communication and Computer Systems, School of Electrical and Computer Engineering, National Technical University of Athens, Athens, Greece.
Department of Radiation Oncology, University Medical Center Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Front Physiol. 2025 Feb 24;16:1434739. doi: 10.3389/fphys.2025.1434739. eCollection 2025.
Prostate cancer (PCa) is the most frequent diagnosed malignancy in male patients in Europe and radiation therapy (RT) is a main treatment option. However, current RT concepts for PCa have an imminent need to be rectified in order to modify the radiotherapeutic strategy by considering (i) the personal PCa biology in terms of radio resistance and (ii) the individual preferences of each patient.
To this end, a mechanistic multiscale model of prostate tumor response to external radiotherapeutic schemes, based on a discrete entity and discrete event simulation approach has been developed. Following technical verification, an adaptation to clinical data approach is delineated. Multiscale data has been provided by the University of Freiburg. Additionally, a sensitivity analysis has been performed.
The impact of model parameters such as cell cycle duration, dormant phase duration, apoptosis rate of living and progenitor cells, fraction of dormant stem and progenitor cells that reenter cell cycle, number of mitoses performed by progenitor cells before becoming differentiated, fraction of stem cells that perform symmetric division, fraction of cells entering the dormant phase following mitosis, alpha and beta parameters of the linear-quadratic model and oxygen enhancement ratio has been studied. The model has been shown to be particularly sensitive to the apoptosis rate of living stem and progenitor cells, the fraction of dormant stem and progenitor cells that reenter cell cycle, the fraction of stem cells that perform symmetric division and the fraction of cells entering the dormant phase following mitosis. A qualitative agreement of the model behavior with experimental and clinical knowledge has set the basis for the next steps towards its thorough clinical validation and its eventual certification and clinical translation. The paper showcases the feasibility, the fundamental design and the qualitative behavior of the model in the context of experimentation.
Further data is being collected in order to enhance the model parametrization and conduct extensive clinical validation. The envisaged digital twin or OncoSimulator, a concept and technologically integrated system that our team has previously developed for other cancer types, is expected to support both patient personalized treatment and clinical trials.
前列腺癌(PCa)是欧洲男性患者中最常被诊断出的恶性肿瘤,放射治疗(RT)是主要的治疗选择。然而,当前针对PCa的放疗理念迫切需要修正,以便通过考虑以下因素来调整放疗策略:(i)前列腺癌在放射抗性方面的个体生物学特性;(ii)每位患者的个人偏好。
为此,基于离散实体和离散事件模拟方法,开发了一种前列腺肿瘤对外部放疗方案反应的多尺度机制模型。在技术验证之后,描述了一种适应临床数据的方法。多尺度数据由弗莱堡大学提供。此外,还进行了敏感性分析。
研究了模型参数的影响,如细胞周期持续时间、休眠期持续时间、存活细胞和祖细胞的凋亡率、重新进入细胞周期的休眠干细胞和祖细胞的比例、祖细胞在分化前进行的有丝分裂次数、进行对称分裂的干细胞比例、有丝分裂后进入休眠期的细胞比例、线性二次模型的α和β参数以及氧增强比。结果表明,该模型对存活干细胞和祖细胞的凋亡率、重新进入细胞周期的休眠干细胞和祖细胞的比例、进行对称分裂的干细胞比例以及有丝分裂后进入休眠期的细胞比例特别敏感。该模型行为与实验和临床知识的定性一致性为其全面临床验证、最终认证和临床转化的后续步骤奠定了基础。本文展示了该模型在实验背景下的可行性、基本设计和定性行为。
正在收集更多数据,以完善模型参数设置并进行广泛的临床验证。我们团队之前为其他癌症类型开发的概念和技术集成系统——设想中的数字孪生或肿瘤模拟器,有望支持患者个性化治疗和临床试验。