A method of testing postnatal carcinogenicity in rats was elaborated.
The substances to be tested were administered from the 1st day after b
irth to the 5th, 10th and 20th days of age. The subsequent supply of a
substance in diet from weaning (28th day of age) up to the end of the
first year of survival was an optimal combination. A total of 12 subs
tances were tested by this method. For all substances it was possible
to provide a comparison with the results of long-term studies. For nin
e substances carcinogenicity was demonstrated in both tests, out of th
em in eight cases in identical organ systems. In three cases no carcin
ogenicity was ascertained in the postnatal study, in two compounds ide
ntical negative results were obtained by the two approaches. In one ca
se (the cytostatic TS-160) development of sarcomas was found at the si
te of subcutaneous administration in the long-term study, and this eff
ect was not observed in the postnatal study. Results identical for the
two methods (carcinogenic or noncarcinogenic) were achieved in 11 sub
stances, i.e. 91.7%. In addition, in 10 compounds, for which carcinoge
nicity was demonstrated either in the postnatal study or in the long-t
erm study, the occurrence of tumors was found in identical organ syste
ms after 8 compounds which is an 80% agreement in mice, this identity
of organs was demonstrated only in 62.5% of the compounds tested. The
present results demonstrated that the use the postnatal carcinogenicit
y lest in rats offers the determination of possible carcinogenic effec
t of the compound tested with a high probability, under economically m
ore advantageous conditions, and with almost the same qualitative resu
lts as with the use of the long-term tests for carcinogenicity.