Non-linearity in cancer dose-response: The role of exposure duration

IF 3.1 Q2 TOXICOLOGY
Andrey A. Korchevskiy , Arseniy Korchevskiy
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引用次数: 2

Abstract

Context

An apparent deviation from nonlinearity in cancer dose-response was reported for various carcinogens. In particular, some studies hypothesized that in mesothelioma, the exposure-response relationship can be modelled as a power function with exponent from 0.6 to 1. However, various factors can affect the shape of the dose-response, producing the apparent supralinear trend.

Objective

To develop a mathematical model that would demonstrate a relationship of mesothelioma lifetime risk and exposure duration, with various assumptions about a hazard rate function.

Methods

Two different hazard rate functions – the Peto model and the two-stage clonal expansion (TSCE) model – were considered. The analytical formulas for lifetime risk were developed, with and without a lifetable correction. Standard calculus methods were applied to test the shape of the lifetime risk curve.

Results

For both Peto and TSCE models, it was shown that mesothelioma lifetime risk changes supralinearly with duration; the exponent of the power function was ranging from 0.68 to 0.89. However, the dose-response curve by cumulative exposure is close to linearity and is linear if the exposure duration would be constant. The model has been tested for chrysotile asbestos cohorts, with a good agreement demonstrated with published mesothelioma excess mortality (R=0.88, p<0.0041).

Conclusion

For mesothelioma, the observed deviation from linearity in the dose-response relationship can be potentially explained by the impact of a change in the duration of exposure. In a meta-analysis, this deviation can be eliminated by standardizing the mortality data for various cohorts by duration of exposure.

Short Abstract

An apparent deviation from nonlinearity in cancer dose-response was reported for various carcinogens. We applied two different hazard rate equations – the Peto model and the two-stage clonal expansion (TSCE) model – to pleural mesothelioma mortality. The analytical formulas for lifetime risk were developed. For both the Peto and TSCE models, it was shown that mesothelioma lifetime risk changes supralinearly with duration. However, the dose-response curve for cumulative exposure is close to linearity.

癌症剂量反应的非线性:暴露持续时间的作用
据报道,各种致癌物的剂量反应明显偏离非线性。特别是,一些研究假设在间皮瘤中,暴露-反应关系可以建模为指数从0.6到1的幂函数。然而,各种因素可以影响剂量反应的形状,产生明显的超线性趋势。目的建立间皮瘤终生风险与暴露时间关系的数学模型,并对危险率函数进行各种假设。方法采用Peto模型和两期克隆扩增(TSCE)模型进行风险率分析。开发了终生风险的分析公式,有或没有生命表校正。采用标准演算方法检验终身风险曲线的形状。结果Peto模型和TSCE模型均显示间皮瘤终生风险随病程呈超线性变化;幂函数的指数范围为0.68 ~ 0.89。然而,累积暴露的剂量-反应曲线接近线性,如果暴露时间一定,则是线性的。该模型已在温石棉队列中进行了测试,与已公布的间皮瘤超额死亡率(R=0.88, p<0.0041)有很好的一致性。结论对于间皮瘤,观察到的剂量-反应关系的线性偏差可以用暴露时间变化的影响来解释。在荟萃分析中,可以通过按暴露时间对不同队列的死亡率数据进行标准化来消除这种偏差。摘要据报道,各种致癌物的剂量反应明显偏离非线性。我们应用了两种不同的风险率方程——Peto模型和两期克隆扩张(TSCE)模型——来计算胸膜间皮瘤的死亡率。建立了终身风险的分析公式。Peto和TSCE模型均显示间皮瘤终生风险随病程呈超线性变化。然而,累积暴露的剂量-反应曲线接近线性。
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
Computational Toxicology
Computational Toxicology Computer Science-Computer Science Applications
CiteScore
5.50
自引率
0.00%
发文量
53
审稿时长
56 days
期刊介绍: Computational Toxicology is an international journal publishing computational approaches that assist in the toxicological evaluation of new and existing chemical substances assisting in their safety assessment. -All effects relating to human health and environmental toxicity and fate -Prediction of toxicity, metabolism, fate and physico-chemical properties -The development of models from read-across, (Q)SARs, PBPK, QIVIVE, Multi-Scale Models -Big Data in toxicology: integration, management, analysis -Implementation of models through AOPs, IATA, TTC -Regulatory acceptance of models: evaluation, verification and validation -From metals, to small organic molecules to nanoparticles -Pharmaceuticals, pesticides, foods, cosmetics, fine chemicals -Bringing together the views of industry, regulators, academia, NGOs
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