Peer Review in Toxicologic Pathology

Author:

Ward Jerrold M.1,Hardisty Jerry F.2,Hailey James R.3,Streett C. Spencer4

Affiliation:

1. National Cancer Institute, Frederick, Maryland 21702-1201

2. Experimental Pathology Laboratories, Inc., Research Triangle Park, North Carolina 27709

3. National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina 27709

4. International Research and Development Corporation, Mattawan, Michigan 49071

Abstract

Peer review of histopathology findings in safety assessment studies involving rodents and other animals is a relatively recent procedure in toxicologic pathology. It serves to ensure the integrity of the pathology evaluation in safety studies, encourages consistency of diagnostic criteria and use of common terminology, and provides a method of continuing education for participants. The use of a standardized system of pathology nomenclature and diagnostic criteria, such as the Society of Toxicologic Pathologist's Guides for Toxicologic Pathology, is of great value in the procedure. Pathology reviews may involve government-sponsored bioassay programs, in-house industrial corporations, or individual peer reviews suggested or required by government regulatory agencies. Pathology Working Groups can be an integral part of the review process. The extent of the peer review is primarily dependent on the study results; however, other variables such as confidence of the data, study size and duration, complexity, and purpose are also important considerations. Essential components of any peer review, however, include selection of tissues/lesions for review, by a reviewing pathologist, discrepancy resolution, data modification, and documentation of all aspects of the review process. Specific procedures for pathology peer review are discussed. Disagreements among pathologists discovered in peer reviews can be resolved by several methods and examples will be presented. The entire pathology peer review process should be a learning experience for all involved and can help ensure the integrity of animal toxicology studies used for important regulatory decisions involving the use of chemicals in our society.

Publisher

SAGE Publications

Subject

Cell Biology,Toxicology,Molecular Biology,Pathology and Forensic Medicine

Reference26 articles.

1. Boorman GA and Eustis SL (1986). The pathology working group as a means for assuring pathology quality in toxicological studies. In: Managing Conduct and Data Quality of Toxicology Studies, KB Hoover, JK Baldwin, AF Velner, CE Whitmire , CL Davies, and DW Bristol (eds). Princeton Scientific Publishing, Princeton, New Jersey, pp. 271-275.

2. Boorman GA, Eustis SL, Elwell MR, Montgomery CA Jr, and MacKenzie WF (1990). Pathology of the Fischer Rat. Academic Press, San Diego. 580 pp.

3. Boorman GA, Montgomery CA Jr, Eustis SL, Wolfe MJ, McConnell EE, and Hardisty JF (1985). Quality assurance in pathology for rodent carcinogenicity studies. In: Handbook of Carcinogen Testing, HA Milman and EK Weisburger (eds). Noyes Publications, Park Ridge, New Jersey, pp. 345-357.

4. Frith CH and Ward JM (1988). Color Atlas of Neoplastic and Non-Neoplastic Lesions in Aging Mice. Elsevier, Amsterdam . 109 pp.

5. Hepatotoxicity and carcinogenicity in female Sprague-Dawley rats treated with 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD): A pathology working group reevaluation

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