Lessons learned in applying the US EPA proposed cancer guidelines to specific compounds

被引:47
作者
Andersen, ME
Meek, ME
Boorman, GA
Brusick, DJ
Cohen, SM
Dragan, YP
Frederick, CB
Goodman, JI
Hard, GC
O'Flaherty, EJ
Robinson, DE
机构
[1] ILSI Hlth & Environm Sci Inst, Washington, DC 20036 USA
[2] Colorado State Univ, Dept Environm Hlth, Ft Collins, CO 80523 USA
[3] NIEHS, Res Triangle Pk, NC 27709 USA
[4] Covance Labs, Harrogate, England
[5] Univ Nebraska, Med Ctr, Lincoln, NE 68583 USA
[6] Ohio State Univ, Columbus, OH 43210 USA
[7] Rohm & Haas Co, Philadelphia, PA 19105 USA
[8] Michigan State Univ, E Lansing, MI 48824 USA
[9] Amer Hlth Fdn, New York, NY 10017 USA
[10] Univ Cincinnati, Cincinnati, OH 45221 USA
关键词
chloroform; dichloroacetic acid; proposed cancer guidelines; US EPA; mode of action; margin of exposure; harmonization; modeling; toxicokinetic; evidence; preponderance of; risk assessment;
D O I
10.1093/toxsci/53.2.159
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
An expert panel was convened to evaluate the U.S. Environmental Protection Agency's "Proposed Guidelines for Carcinogen Risk Assessment" through their application to data sets for chloroform (CHCl3) and dichloroacetic acid (DCA). The panel also commented on perceived strengths and limitations encountered in applying the guidelines to these specific compounds. This latter aspect of the panel's activities is the focus of this perspective. The panel was very enthusiastic about the evolution of these proposed guidelines, which represent a major step forward from earlier EPA guidance on cancer-risk assessment. These new guidelines provide the latitude to consider diverse scientific data and allow considerable flexibility in dose-response assessments, depending on the chemical's mode of action. They serve as a very useful template for incorporating state-of-the-art science into carcinogen risk assessments. In addition, the new guidelines promote harmonization of methodologies for cancer- and noncancer-risk assessments. While new guidance on the qualitative decisions ensuing from the determination of mode of action is relatively straightforward, the description of the quantitative implementation of various risk-assessment options requires additional development. Specific areas needing clarification include: (1) the decision criteria for judging the adequacy of the weight of evidence for any particular mode of action; (2) the role of mode of action in guiding development of toxicokinetic, biologically based or case-specific models; (3) the manner in which mode of action and other technical considerations provide guidance on margin-of-exposure calculations; (4) the relative roles of the risk manager versus the risk assessor in evaluating the margin of exposure; and (5) the influence of mode of action in harmonizing cancer and noncancer risk assessment methodologies. These points are elaborated as recommendations for improvements to any revisions. In general, the incorporation of examples of quantitative assessments for specific chemicals would strengthen the guidelines. Clearly, any revisions should retain the emphasis present in these draft guidelines on flexibility in the use of scientific information with individual compounds, while simultaneously improving the description of the processes by which these mode-of-action data are organized and interpreted.
引用
收藏
页码:159 / 172
页数:14
相关论文
共 86 条
[1]   MULTIPLE ACTIVATION OF CHLOROFORM IN KIDNEY MICROSOMES FROM MALE AND FEMALE DBA/2J MICE [J].
ADE, P ;
GUASTADISEGNI, C ;
TESTAI, E ;
VITTOZZI, L .
JOURNAL OF BIOCHEMICAL TOXICOLOGY, 1994, 9 (06) :289-295
[2]   PHYSIOLOGICALLY BASED PHARMACOKINETICS AND THE RISK ASSESSMENT PROCESS FOR METHYLENE-CHLORIDE [J].
ANDERSEN, ME ;
CLEWELL, HJ ;
GARGAS, ML ;
SMITH, FA ;
REITZ, RH .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1987, 87 (02) :185-205
[3]  
[Anonymous], 1994, SCI JUDGM RISK ASS
[4]  
[Anonymous], 1998, FED REGISTER, V63, P69390
[5]  
[Anonymous], 1996, HLTH CRIT OTH SUPP I, V2
[6]  
[Anonymous], EV EPAS PROP GUID CA
[7]  
[Anonymous], 1986, Federal Register
[8]   Harmonization: Developing consistent guidelines for applying mode of action and dosimetry information to cancer and noncancer risk assessment [J].
Barton, HA ;
Andersen, ME ;
Clewell, HJ .
HUMAN AND ECOLOGICAL RISK ASSESSMENT, 1998, 4 (01) :75-115
[9]   A biologically based risk assessment for vinyl acetate-induced cancer and noncancer inhalation toxicity [J].
Bogdanffy, MS ;
Sarangapani, R ;
Plowchalk, DR ;
Jarabek, A ;
Andersen, ME .
TOXICOLOGICAL SCIENCES, 1999, 51 (01) :19-35
[10]  
BORGHOFF SJ, 1994, TOXICOLOGIST, V14, P43