Update on genotoxicity and carcinogenicity testing of 472 marketed pharmaceuticals

被引:83
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
相关论文
共 404 条
[1]  
Abe S., 1980, KROMOSOMO 2, V20, P574
[2]   Calcium channel blockers and cancer: Is there preclinical evidence for an association? [J].
Ahr, HJ ;
Bomhard, E ;
Mager, H ;
Schluter, G .
CARDIOLOGY, 1997, 88 :68-72
[3]   CHROMOSOME ABERRATION AND SISTER CHROMATID EXCHANGE TEST-RESULTS WITH 42 CHEMICALS [J].
ANDERSON, BE ;
ZEIGER, E ;
SHELBY, MD ;
RESNICK, MA ;
GULATI, DK ;
IVETT, JL ;
LOVEDAY, KS .
ENVIRONMENTAL AND MOLECULAR MUTAGENESIS, 1990, 16 :55-137
[4]  
ANDO N, 1994, YAKURI CHIRYO S5, V22, pS1171
[5]   Chronic long-term nitrate therapy: possible cytogenetic effect in humans? [J].
Andreassi, MG ;
Picano, E ;
Del Ry, S ;
Botto, N ;
Colombo, MG ;
Giannessi, D ;
Lubrano, V ;
Vassalle, C ;
Biagini, A .
MUTAGENESIS, 2001, 16 (06) :517-521
[6]   MUTAGENICITY OF AMINE DRUGS AND THEIR PRODUCTS OF NITROSATION [J].
ANDREWS, AW ;
LIJINSKY, W ;
SNYDER, SW .
MUTATION RESEARCH, 1984, 135 (02) :105-108
[7]  
[Anonymous], 1987, TOXICOL ASSESS
[8]  
[Anonymous], 2004, International Agency for Research on Cancer Monographs on the Evaluation of Carcinogenic Risks to Humans, Volume 84, Some Drinking-water Disinfectants and Contaminants, including Arsenic, V84
[9]  
[Anonymous], 1999, IARC MON EV CARC RIS
[10]  
[Anonymous], IARC MON EV CARC RIS