A multilevel probabilistic dose response model for radiation-induced Harderian gland tumor prevalence–single beam and mixed field effects

IF 3.3 3区 生物学 Q2 ASTRONOMY & ASTROPHYSICS
Life Sciences in Space Research Pub Date : 2026-07-01 Epub Date: 2025-09-17 DOI:10.1016/j.lssr.2025.09.006
Xiaojing Xu, Steve Blattnig, Tony Slaba
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引用次数: 0

Abstract

Space radiation exposure is one of the main risks faced by crewmembers during exploration missions. Currently, the greatest uncertainty in radiation-induced cancer risk estimation for spaceflight missions is in the calculation of the quality factor (QF) largely due to limited ground-based experimental data for the vast range of radiation types found in space. Such data are needed to guide and validate dose-response models and subsequent calculations of relative biological effectiveness (RBE) used for QF assignment. In this work, a dose-response model is developed on the basis of probabilistic arguments and considers processes occurring at the cellular and tissue levels that ultimately result in radiation induced tumorigenesis. Probabilistic methods are extensively relied upon within the model development, so that the dose dependence is ultimately guided by the probability laws rather than any a priori assumption, such as linearity. Model components account for tumor occurrence due to targeted effects (TE), including cell sterilizations, and non-targeted effects (NTE). The model is developed for both single mono-energetic ion beam exposures and mixed field exposures (i.e., involving more than one particle type and energy). The model is calibrated with global fittings to the Harderian gland tumor incidence observations for acute irradiation from single beams reported in Alpen et al. (1993, 1994) and Chang et al. (2016). Both the TE-only model (with NTE opted out) and TE-NTE model fit the observations well, with the latter slightly better for the experiments with high linear energy transfer radiations. Importantly, the model parameters calibrated using single-ion data are then used to make tumorigenesis predictions for mixed field experimental data, as measured by Huang et al. (2020). It is found that the model can predict mixed field irradiations given sufficient single-ion data to allow robust parameter calibration. Mixed-field RBE calculations are performed with the validated model and compared to results obtained with linear dose-response and simple additivity models.
辐射诱发哈德氏腺肿瘤发病率的多水平概率剂量响应模型——单束和混合场效应。
空间辐射暴露是宇航员在探索任务中面临的主要风险之一。目前,航天飞行任务辐射致癌风险估计中最大的不确定性在于质量因子的计算,这主要是由于空间中发现的大量辐射类型的地面实验数据有限。需要这些数据来指导和验证用于QF分配的剂量-反应模型和随后的相对生物有效性(RBE)计算。在这项工作中,剂量-反应模型是在概率论证的基础上发展起来的,并考虑了在细胞和组织水平上发生的最终导致辐射诱导肿瘤发生的过程。在模型开发过程中广泛使用概率方法,因此剂量依赖性最终由概率定律而不是任何先验假设(如线性)指导。模型成分考虑了由于靶向效应(TE)引起的肿瘤发生,包括细胞灭菌和非靶向效应(NTE)。该模型适用于单能量离子束暴露和混合场暴露(即涉及一种以上粒子类型和能量)。该模型是根据Alpen等人(1993,1994)和Chang等人(2016)报道的单束急性照射的哈德氏腺肿瘤发生率观察数据进行全局拟合的。纯te模型(选择不使用NTE)和TE-NTE模型都能很好地拟合观测值,后者对具有高线性能量传递辐射的实验略好一些。重要的是,使用单离子数据校准的模型参数然后用于对混合现场实验数据进行肿瘤发生预测,如Huang等人(2020)所测量的那样。结果表明,在给定足够的单离子数据的情况下,该模型可以预测混合场辐照,从而实现鲁棒参数校准。用验证模型进行了混合场RBE计算,并与线性剂量响应模型和简单加性模型的结果进行了比较。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Life Sciences in Space Research
Life Sciences in Space Research Agricultural and Biological Sciences-Agricultural and Biological Sciences (miscellaneous)
CiteScore
5.30
自引率
8.00%
发文量
69
期刊介绍: Life Sciences in Space Research publishes high quality original research and review articles in areas previously covered by the Life Sciences section of COSPAR''s other society journal Advances in Space Research. Life Sciences in Space Research features an editorial team of top scientists in the space radiation field and guarantees a fast turnaround time from submission to editorial decision.
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