Table 1.
Gender/tumor type | EtO concentration (time-weighted average)a | |||
---|---|---|---|---|
NTP (1987) 2-year bioassay of B6C3F1 miceb,c | ||||
0 ppm | 50 ppm (16.3 mg/m3) | 100 ppm (32.7 mg/m3) | ||
Males | ||||
Lung adenomas plus carcinomas | 11/49 | 19/49 | 26/49* | |
Females | ||||
Lung adenomas plus carcinomas | 2/44 | 5/44 | 22/49* | |
Malignant lymphoma | 9/44 | 6/44 | 22/49* | |
Uterine carcinoma | 0/44 | 1/44 | 5/49j | |
Mammary carcinoma | 1/44 | 8/44* | 6/49 | |
Lynch et al. (1984) 2-year bioassay of male F344 ratsd,e | ||||
0 ppm | 50 ppm (19.1 mg/m3) | 100 ppm (38.1 mg/m3) | ||
Splenic mononuclear cell leukemia | 24/77 | 38/79* | 30/76 | |
Testicular peritoneal mesothelioma | 3/78 | 9/79 | 21/79* | |
Brain mixed-cell glioma | 0/76 | 2/77 | 5/79* | |
(Garman et al. (1985); Snellings et al. (1984)) 2-year bioassay of F344 ratsa,f,g | ||||
0 ppmh | 10 ppm (3.27 mg/m3) | 33 ppm (10.8 mg/m3) | 100 ppm (32.7 mg/m3) | |
Males | ||||
Splenic mononuclear cell leukemia | 13/97 (13%)i | 9/51 (18%) | 12/39* (32%) | 9/30* (30%) |
Testicular peritoneal mesothelioma | 2/97 (2.1%) | 2/51 (3.9%) | 4/39 (10%) | 4/30* (13%) |
Primary brain tumors | 1/181 (0.55%) | 1/92 (1.1%) | 5/85* (5.9%) | 7/87* (8.1%) |
Females | ||||
Splenic mononuclear cell leukemia | 11/116 (9.5%) | 11/54* (21%) | 14/48* (30%) | 15/26* (58%) |
Primary brain tumors | 1/188 (0.53%) | 1/94 (1.1%) | 3/92 (3.3%) | 4/80* (5%) |
Adjusted to continuous exposure; 1 ppm = 1.83 mg/m3.
Exposed 6 hr/d, 5 d/wk.
Incidence data were adjusted by the EPA by eliminating the animals that died prior to the occurrence of the first tumor or prior to 52 wk, whichever was earlier. No treatment-related effects on survival or body weight were observed.
Exposed 7 hr/d, 5 d/wk.
Mean body weights were statistically significantly decreased in both treated groups compared with controls, and increased mortality was observed in the treated groups, with the increase statistically significant in the 100-ppm exposure group (p < 0.01). The individual animal data for this study were not available.
Significant decreases in mean body weight were observed in the 100-ppm exposure group in males and in the 100-ppm and 33-ppm exposure groups in females. Mortality was statistically significantly increased in the 100-ppm exposure groups of both sexes.
Denominators refer to the number of animals for which histopathological diagnosis was performed. For brain tumors, Garman et al. (1985) included animals in the 18-month and the 24-month kills and found dead or euthanized moribund of those alive at the time of the first brain tumor, whereas for the other sites, Snellings et al. (1984) included animals only at the 24-month kill.
Results for two control groups combined.
Numbers in parentheses indicate percentage incidence values.
p = 0.058 by pairwise Fisher’s exact test compared to concurrent controls; however, uterine carcinomas are rare tumors in female B6C3F1 mice, and p < 0.0001 by pairwise Fisher’s exact test compared to the NTP historical control incidence of 1/1,077 for inhalation (air) for female B6C3F1 mice fed with the NIH-07 diet.
p < 0.05 by pairwise Fisher’s exact test.