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Modeling of cell inactivation and carcinogenesis in the atomic bomb survivors with applications to the mortality from all solid, stomach and liver cancer

机译:模拟原子弹幸存者中的细胞失活和致癌作用,并将其应用于所有实体癌,胃癌和肝癌的死亡率

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The two-stage clonal expansion (TSCE) model of carcinogenesis has been applied to cancer mortality data from the atomic bomb survivors, to examine the possible influence of radiation-induced cell inactivation on excess relative risk (ERR) and excess absolute risk (EAR) estimates. Cell survival curve forms being either conventional or allowing for low-dose hypersensitivity (LDH) were investigated. Quality-of-fit tests for non-nested models were used in comparisons with the types of empirical risk models applied at the Radiation Effects Research Foundation (RERF) in Hiroshima. In general the TSCE model was found to represent the data more economically (i.e., with fewer parameters for a similarly good description of the data) than the empirical risk model. However, the data are not strong enough to give a clear preference to one of the very different model types used. Central ERR and EAR estimates (at 1 Sv, for age at exposure 30 and age attained 70) from TSCE and empirical models were in good agreement with each other and with previously published estimates. However, the TSCE models including radiation-induced cell inactivation resulted in a lower estimate of the relative risk at young ages at exposure (0-15 years) than the empirical model. Also the TSCE model allowing for radiation-induced cell inactivation with a conventional cell survival curve resulted at 0.2 Sv in significantly lower risk estimates than the model with LDH. These model differences have been used here to suggest risk estimates which include model uncertainty as well as the usual statistical uncertainty. Model uncertainties were small for central estimates and larger for other values of the variables. Applying the proposed method to excess risk for all solid cancer at 1 Sv, age at exposure 10 and age attained 70, results in total uncertainty ranges that are wider than the pure statistical uncertainty range by about 30% for both ERR and EAR.
机译:已将癌变的两阶段克隆扩展(TSCE)模型应用于来自原子弹幸存者的癌症死亡率数据,以检查辐射诱导的细胞失活对超额相对风险(ERR)和超额绝对风险(EAR)的可能影响估计。研究了常规或允许低剂量超敏反应(LDH)的细胞存活曲线形式。将非嵌套模型的拟合质量测试与广岛辐射效应研究基金会(RERF)应用的经验风险模型的类型进行了比较。一般而言,发现TSCE模型比经验风险模型更经济地表示数据(即,对于相似的良好描述,参数较少)。但是,数据不足以明显地偏爱所使用的非常不同的模型类型之一。 TSCE和经验模型的中心ERR和EAR估计(在1 Sv时,暴露年龄为30岁,达到70岁)彼此之间以及与先前发表的估计值相互吻合。但是,包括辐射诱导的细胞失活在内的TSCE模型导致的年轻风险(0-15岁)的相对风险估算值低于经验模型。同样,TSCE模型允许以常规细胞存活曲线进行辐射诱导的细胞灭活,其结果为0.2 Sv,其风险估算值明显低于LDH模型。这些模型差异已用于建议风险估计,其中包括模型不确定性以及通常的统计不确定性。对于中央估计,模型不确定性较小,而对于其他变量值,模型不确定性较大。将提出的方法应用于所有实体癌在1 Sv,暴露年龄10和达到70岁时的超高风险,导致ERR和EAR的总不确定性范围比纯统计不确定性范围宽约30%。

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