Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 4 de 4
Filter
Add more filters










Database
Language
Publication year range
1.
Fundam Appl Toxicol ; 7(4): 573-84, 1986 Nov.
Article in English | MEDLINE | ID: mdl-3803752

ABSTRACT

Tumor incidence data from 18 recently completed carcinogenicity studies utilizing male and female mice and rats were examined to determine if the frequency of significant (p less than 0.05) pairwise differences between the two concurrent control groups employed in these experiments exceeded chance expectation. Although marked study-to-study variability was observed for some tumors, no evidence of extra-binomial within-study variability between the two concurrent control groups was found. The total number of observed significant (p less than 0.05) paired-control differences was virtually identical to what would be expected from the usual binomial model assumptions; the corresponding overall observed (44%) and expected (47-50%) false positive rates were essentially the same. While one should not overgeneralize the implications of these findings, these results should lessen concerns that elevated false positive rates resulting from extra-binomial within-study variability might be adversely affecting the interpretation of long-term laboratory animal carcinogenicity studies. On the other hand, these results reaffirm the conclusions of other investigators that (particularly for commonly occurring tumors) more stringent evidence than an isolated p less than 0.05 effect should be required before an increased tumor incidence is regarded as biologically significant; otherwise, the study may have an unacceptably high false positive rate.


Subject(s)
Carcinogens/toxicity , False Positive Reactions , Neoplasms, Experimental/pathology , Analysis of Variance , Animals , Animals, Laboratory , Female , Male , Mice , Rats , Sex Factors , Species Specificity
2.
Fundam Appl Toxicol ; 4(3 Pt 2): S395-401, 1984 Jun.
Article in English | MEDLINE | ID: mdl-6745557

ABSTRACT

Risk assessment of food-borne carcinogens is becoming a common practice at FDA. Actual risk is not being estimated, only the upper limit of risk. The risk assessment process involves a large number of steps and assumptions, many of which affect the numerical value estimated. The mathematical model which is to be applied is only one of the factors which affect these numerical values. To fulfill the policy objective of using the "worst plausible case" in estimating the upper limit of risk, recognition needs to be given to a proper balancing of assumptions and decisions. Interaction between risk assessors and risk managers should avoid making or giving the appearance of making specific technical decisions such as the choice of the mathematical model. The importance of this emerging field is too great to jeopardize it by inappropriately mixing scientific judgments with policy judgments. The risk manager should understand fully the points and range of uncertainty involved in arriving at the estimates of risk which must necessarily affect the choice of the policy or regulatory options available.


Subject(s)
Carcinogens, Environmental/adverse effects , Food/standards , Animals , Food Additives/toxicity , Food Contamination , Hair Dyes/toxicity , Humans , Legislation, Drug , Models, Biological , Risk , Risk Management , Sweetening Agents/toxicity , United States , United States Food and Drug Administration
SELECTION OF CITATIONS
SEARCH DETAIL
...