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Table 1: Tumor incidence data in rats and mice exposed to ethylene dichloride (NCI, 1978).<br />

Tumor Type<br />

Male rats<br />

Squamous cell carcinoma<br />

(forestomach)<br />

Exposure Concentration (mg/kg-day)<br />

0 47 95<br />

0/60 3/50 9/50*<br />

Hemangiosarcoma 1/60 9/50* 7/50*<br />

Female rats<br />

Hemangiosarcoma 0/59 4/50* 4/50*<br />

Mammary adenomas 1/59 1/50 18/50*<br />

Male mice<br />

Exposure Concentration (mg/kg-day)<br />

0 97 195<br />

Hepatocellular carcinomas 4/59 6/47 12/48*<br />

Alveolar/bronchiolar<br />

adenomas<br />

Female mice<br />

Alveolar/bronchiolar<br />

adenomas<br />

0/59 1/47 15/48*<br />

Exposure Concentration (mg/kg-day)<br />

0 149 299<br />

2/60 7/50* 15/48*<br />

Mammary adenocarcinoma 0/60 9/50* 7/48*<br />

Endometrial polyp or<br />

stromal sarcomas<br />

0/60 5/49* 5/47*<br />

*Significantly increased incidence in treated animals compared with pooled vehicle controls; significance<br />

calculated using Fisher Exact Test (one-tailed); p ≤ 0.05.<br />

Maltoni et al. (1980) conducted extensive inhalation carcinogenicity studies in Sprague-Dawley rats and<br />

Swiss mice. Four groups, each consisting of 180 rats or mice of both sexes, were exposed to EDC<br />

concentrations of 5, 10, 50, or 150-250 ppm, respectively, seven hours/day, five days/week, for 78<br />

weeks. Two groups of 180 rats per sex, or one group of 249 mice, served as controls. Although all<br />

animals received a lifetime exposure and extensive histopathology was performed on each animal, no<br />

significant increased in tumor incidences were seen (Maltoni et al., 1980).<br />

289

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