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啮齿动物致癌性研究中历史对照数据的使用。

Use of historical control data in carcinogenicity studies in rodents.

作者信息

Haseman J K, Huff J, Boorman G A

机构信息

Biometry and Risk Assessment Program, National Institute of Environmental Health Sciences, Research Triangle Park, NC 27709, USA.

出版信息

Toxicol Pathol. 1984;12(2):126-35. doi: 10.1177/019262338401200203.

Abstract

This paper considers the use of historical control data in the evaluation of tumor incidences from carcinogenicity studies in rodents. Although the most appropriate control group for interpretative purposes is always the concurrent control, there are instances in which the use of historical control information can aid an investigator in the overall evaluation of tumor incidence data. One example is rare tumors; another is a tumor that shows a marginally significant result relative to concurrent controls. However, before historical control data can be used in a formal testing framework, a number of important issues must first be considered. The nomenclature conventions and diagnostic criteria for each study should be identical to insure unambiguous identification of all relevant tumors in the historical control database. Criteria should be established that will aid in determining whether a particular study should be included in the database. This will assure a homogeneous set of studies upon which to base statistical comparisons. Since study-to-study variability in tumor rates may exceed what would be expected by chance alone, these sources of variability should be identified and controlled. Finally, statistical procedures should be employed that adjust for extra-binomial variability. This paper also summarizes tumor incidence data from untreated Fischer 344 rats and B6C3F1 mice in the National Toxicology Program (NTP) historical control database. All studies in the database are of two years duration, and all neoplasms occurring with a frequency of 0.5% or more are reported.

摘要

本文探讨了在评估啮齿动物致癌性研究中的肿瘤发生率时使用历史对照数据的情况。尽管从解释目的来看,最合适的对照组始终是同期对照组,但在某些情况下,使用历史对照信息有助于研究人员对肿瘤发生率数据进行全面评估。一个例子是罕见肿瘤;另一个例子是相对于同期对照组显示出边缘显著结果的肿瘤。然而,在将历史对照数据用于正式的测试框架之前,必须首先考虑一些重要问题。每项研究的命名惯例和诊断标准应保持一致,以确保在历史对照数据库中能明确识别所有相关肿瘤。应制定标准,以帮助确定某项特定研究是否应纳入数据库。这将确保有一组同质化的研究可作为统计比较的基础。由于不同研究之间肿瘤发生率的变异性可能超过仅由偶然因素导致的预期变异性,这些变异性来源应予以识别和控制。最后,应采用能针对超二项变异性进行调整的统计程序。本文还总结了国家毒理学计划(NTP)历史对照数据库中未处理的Fischer 344大鼠和B6C3F1小鼠的肿瘤发生率数据。数据库中的所有研究为期两年,所有发生率为0.5%或更高的肿瘤均有报告。

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