Update on genotoxicity and carcinogenicity testing of 472 marketed pharmaceuticals

被引:82
作者
Brambilla, Giovanni [1 ]
Martelli, Antonietta [1 ]
机构
[1] Univ Genoa, Dept Internal Med, Div Clin Pharmacol & Toxicol, Sez Farmacol,DIMI, I-16132 Genoa, Italy
关键词
Marketed drugs; Genotoxicity; Carcinogenicity; GENE-TOX PROGRAM; SISTER-CHROMATID EXCHANGES; BONE-MARROW-CELLS; UNSCHEDULED DNA-SYNTHESIS; SPRAGUE-DAWLEY RATS; CULTURED HUMAN-LYMPHOCYTES; HAMSTER OVARY CELLS; GLYCERYL TRINITRATE NITROGLYCERIN; SALMONELLA MUTAGENICITY TESTS; ADRENERGIC-BLOCKING-AGENTS;
D O I
10.1016/j.mrrev.2008.09.002
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
This survey is a compendium of genotoxicity and carcinogenicity information of 838 marketed drugs, whose expected clinical use is continuous for at least 6 months or intermittent over an extended period of time. Of these 838 drugs, 366 (43.7%) do not have retrievable genotoxicity or carcinogenicity data. The remaining 472 (56.3%) have at least one genotoxicity or carcinogenicity test result. Of the 449 drugs with at least one genotoxicity test result, 183 (40.8%) have at least one positive finding. Of the 338 drugs with at least one carcinogenicity test result, 160 (47.3%) have at least one positive result. Concerning the predictivity of genetic toxicology findings for long-term carcinogenesis assays, of the 315 drugs which have both genotoxicity and carcinogenicity data 116 (36.8%) are neither genotoxic nor carcinogenic, 50 (15.9%) are non-carcinogens which test positive in at least one genotoxicity assay, 75 (23.8%) are carcinogenic in at least one sex of mice or rats but test negative in genotoxicity assays, and 74 (23.5%) are both genotoxic and carcinogenic. Only 208 (24.8%) of the 838 drugs considered have all data required by current guidelines for testing of pharmaceuticals. However, it should be noted that a large fraction of the drugs considered were developed and marketed prior to the present regulatory climate. Although the laws do not require re-testing based on revised standards, in the absence of epidemiological studies excluding a carcinogenic risk to humans, a re-evalutation would be appropriate. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:209 / 229
页数:21
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