Hami Rihab, Apeke Sena, Redou Pascal, Gaubert Laurent, Dubois Ludwig J, Lambin Philippe, Visvikis Dimitris, Boussion Nicolas
INSERM UMR 1101 "LaTIM", CEDEX 3, 29238 Brest, France.
CERV, European Center for Virtual Reality, ENIB, CEDEX 3, 29238 Brest, France.
J Imaging. 2023 Jun 20;9(6):124. doi: 10.3390/jimaging9060124.
Despite the intensive use of radiotherapy in clinical practice, its effectiveness depends on several factors. Several studies showed that the tumour response to radiation differs from one patient to another. The non-uniform response of the tumour is mainly caused by multiple interactions between the tumour microenvironment and healthy cells. To understand these interactions, five major biologic concepts called the "5 Rs" have emerged. These concepts include reoxygenation, DNA damage repair, cell cycle redistribution, cellular radiosensitivity and cellular repopulation. In this study, we used a multi-scale model, which included the five Rs of radiotherapy, to predict the effects of radiation on tumour growth. In this model, the oxygen level was varied in both time and space. When radiotherapy was given, the sensitivity of cells depending on their location in the cell cycle was taken in account. This model also considered the repair of cells by giving a different probability of survival after radiation for tumour and normal cells. Here, we developed four fractionation protocol schemes. We used simulated and positron emission tomography (PET) imaging with the hypoxia tracer 18F-flortanidazole (18F-HX4) images as input data of our model. In addition, tumour control probability curves were simulated. The result showed the evolution of tumours and normal cells. The increase in the cell number after radiation was seen in both normal and malignant cells, which proves that repopulation was included in this model. The proposed model predicts the tumour response to radiation and forms the basis for a more patient-specific clinical tool where related biological data will be included.
尽管放射疗法在临床实践中被广泛应用,但其有效性取决于多个因素。多项研究表明,肿瘤对放疗的反应因患者而异。肿瘤反应的不一致主要是由肿瘤微环境与健康细胞之间的多种相互作用引起的。为了理解这些相互作用,出现了五个主要的生物学概念,即“5R”。这些概念包括再氧合、DNA损伤修复、细胞周期再分布、细胞放射敏感性和细胞再增殖。在本研究中,我们使用了一个多尺度模型,该模型包含放疗的5R,以预测辐射对肿瘤生长的影响。在这个模型中,氧水平在时间和空间上都是变化的。进行放疗时,会考虑细胞根据其在细胞周期中的位置而产生的敏感性。该模型还通过给出肿瘤细胞和正常细胞在辐射后的不同存活概率来考虑细胞的修复。在这里,我们制定了四种分割方案。我们使用模拟和正电子发射断层扫描(PET)成像以及缺氧示踪剂18F-氟替硝唑(18F-HX4)图像作为模型的输入数据。此外,还模拟了肿瘤控制概率曲线。结果显示了肿瘤和正常细胞的演变。在正常细胞和恶性细胞中都观察到了辐射后细胞数量的增加,这证明该模型中包含了再增殖。所提出的模型预测了肿瘤对辐射的反应,并为一个更具患者特异性的临床工具奠定了基础,该工具将纳入相关生物学数据。