Effects of intermittent diethylstilbestrol diphosphate administration on the R3327 rat prostatic carcinoma

• Published in: Cancer research (Chicago, Ill.) Ill.), 1987-11, Vol.47 (22), p.5967-5970
• Main Authors: RUSSO, P, LIGUORI, G, HESTON, W. D. W, HURYK, R, CHI-REI YANG, FAIR, W. R, WHITMORE, W. F, HERR, H. W
• Format: Article
• Language: English
• Subjects: Animals; Antineoplastic agents; Antineoplastic Agents - therapeutic use; Applied sciences; Biological and medical sciences; Body Weight - drug effects; Chemotherapy; Diethylstilbestrol - administration & dosage; Diethylstilbestrol - analogs & derivatives; Diethylstilbestrol - therapeutic use; Diethylstilbestrol - toxicity; Drug Administration Schedule; Exact sciences and technology; Male; Medical sciences; Orchiectomy; Other techniques and industries; Pharmacology. Drug treatments; Prostatic Neoplasms - drug therapy; Rats; Rats, Inbred Strains; Testosterone - blood
• ISSN: 0008-5472; 1538-7445

Clinical trials have utilized intermittent diethylstilbestrol diphosphate (DES) therapy in advanced symptomatic prostatic carcinoma to diminish the morbidity of standard endocrine therapy. To determine the effect of intermittent DES administration on the Dunning R3327 rat prostatic adenocarcinoma 60 days following tumor implant, 6 groups were randomly assigned: control (N = 8), castrate (N = 10), high dose DES (N = 8, 1.6 micrograms/ml DES continuously in drinking water), low dose DES (N = 10, 0.4 microgram/ml continuously in drinking water), intermittent high dose DES (N = 10, 1.6 micrograms/ml DES in drinking water for 1 week, then off for 3 weeks), and intermittent low dose DES (N = 10, 0.4 microgram/ml DES for 1 week, then off for 3 weeks). Results indicate that low or high dose DES, and intermittent low or intermittent high dose DES during the week of administration were able to reduce serum testosterone to castrate levels (0.1 ng/ml). After withdrawal of intermittent DES, serum testosterone returned toward control levels (1.0 ng/ml). Initial mean tumor burden between control and treatment groups was not significantly different. All DES exposed rats had a tumor volume at death (range, 15.6-18.3 cm3) smaller than control (mean, 25.4 cm3) or castrate (mean, 40.8 cm3) rats. Despite this significant survival advantage from the time of randomization was achieved only in castrate (median survival, 331 days) or high dose DES (median survival, 359 days) groups compared to control (median survival, 225 days). Similarly, significant prolongation in tumor doubling time was achieved only by rats receiving castration or high dose DES. Intermittent DES administration controls tumor volume but does not provide a survival advantage. In this respect, intermittent DES is inferior to castration.