Lin K K, Rahman M A
Division of Biometrics II, Food and Drug Administration, Rockville, Maryland 20857, USA.
J Biopharm Stat. 1998 Mar;8(1):1-15; discussion 17-22. doi: 10.1080/10543409808835216.
Based on results of simulation and empirical studies conducted within the Divisions of Biometrics, Center for Drug Evaluation and Research, Food and Drug Administration, and in collaboration with the National Toxicology Program, the Center has recently changed the significance levels for testing positive linear trend in incidence rate for common and rare tumors, respectively, from 0.01 and 0.05 to 0.005 and 0.025. The overall false positive rate resulting from the use of this new rule in the tests for linear trend in a two-species-two-sex study is about 10%, the rate that is judged as the most appropriate in a regulatory setting by the Center. This paper describes two of the studies.
根据食品药品监督管理局药品评价和研究中心生物统计学部门开展的模拟和实证研究结果,并与国家毒理学计划合作,该中心最近分别将常见肿瘤和罕见肿瘤发病率阳性线性趋势检验的显著性水平从0.01和0.05更改为0.005和0.025。在两物种两性研究中,在线性趋势检验中使用这一新规则产生的总体假阳性率约为10%,该中心认为这一比率在监管环境中最为合适。本文描述了其中两项研究。