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线性二次模型作为预测放射后细胞存活的模型的无效性和替代方法。

Invalidity of, and alternative to, the linear quadratic model as a predictive model for postirradiation cell survival.

机构信息

Department of Radiation Oncology and Molecular Radiation Sciences, Johns Hopkins University, 401 N. Broadway, Baltimore, Maryland, 21287, USA.

出版信息

Cancer Sci. 2023 Jul;114(7):2931-2938. doi: 10.1111/cas.15796. Epub 2023 Apr 5.

Abstract

The linear quadratic (LQ) model has been the dominant tool in preclinical radiobiological modeling of cell survival as a function of dose. However, as a second-order polynomial approximation, it suffers from two well-known pitfalls: nonmonotonic behavior and poor extrapolation. This study examined the raw data of 253 sets of photons and 943 sets of the ion beam from the Particle Irradiation Data Ensemble (PIDE) project to understand how often the LQ model could result in a negative β, which would give unrealistic predictions. Additionally, the predictive performance of the LQ model, the power model, and the linear model's predictive performance was studied using leave-one-out cross-validation (LOOCV) and twofold cross-validation. It was found that, when fitted to the LQ model, 7.5% of the photon and 29.8% of the ion beam dose-response data would result in negative β, compared to 0.77% and 2.0%, respectively, reported in published works. The LQ model performed poorly in LOOCV compared to the alternative power model, and performed the worst among the three models in twofold cross-validation. The LQ model leads to unrealistic parameters, which are vastly under-reported in published studies, and performs poorly in standard cross-validation tests. Therefore, the LQ model is not a valid predictive dose-response model for cell survival. Alternative models need to be investigated.

摘要

线性二次(LQ)模型一直是作为剂量函数的细胞存活的临床前放射生物学建模的主要工具。然而,作为一个二阶多项式逼近,它存在两个众所周知的缺陷:非单调行为和较差的外推。本研究检查了来自粒子辐照数据集合(PIDE)项目的 253 组光子和 943 组离子束的原始数据,以了解 LQ 模型如何经常导致负的β,这将给出不切实际的预测。此外,使用留一法交叉验证(LOOCV)和两倍交叉验证研究了 LQ 模型、幂律模型和线性模型的预测性能。结果发现,当拟合到 LQ 模型时,7.5%的光子和 29.8%的离子束剂量反应数据将导致负的β,而在已发表的文献中,分别为 0.77%和 2.0%。与替代的幂律模型相比,LQ 模型在 LOOCV 中的表现较差,在两倍交叉验证中表现最差。LQ 模型导致不切实际的参数,这些参数在已发表的研究中被大大低估,并且在标准交叉验证测试中表现不佳。因此,LQ 模型不是细胞存活的有效预测剂量反应模型。需要研究替代模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c118/10323099/fd09c724bafc/CAS-114-2931-g001.jpg

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