Pharmacokinetic studies of 13-cis retinoic acid (13cRA) and all-trans retinoic acid (ATRA), the 2 most commonly used retinoids, have suggested significant differences in the disposition of these compounds despite their structural similarity. In vivo treatment with 13cRA has been associated with 20-3
13-cis-Retinoic acid in chemopreventiion of superficial bladder cancer
โ Scribed by Geroge R. Prout Jr.; Bruce A. Barton; W. W. Kontz Jr.; S. Loening; M. J. Flangan; G. Branen
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 369 KB
- Volume
- 50
- Category
- Article
- ISSN
- 0730-2312
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โฆ Synopsis
Animal studies indicate that 13-cis-retinoic acid (CRA) inhibits bladder tumor growth and is effective in treating patients with serious dermatologic disorders. A trial of CRA in patients at high risk for recurrent Ta, T l tumors was initiated at an experimental dose of 0.5 mg/kg/d in three divided doses, increasing to 1 mglkgld at four weeks. Treatment of twenty eligible patients lasted for six months with an additional 24 month follow-up period. One patient was later excluded due to toxicity resulting in an early dose reduction.
Eight patients stopped treatment before three months; of these five, had recurrences within three months, one developed pulmonary metastasis, and one developed a T2G3 tumor. Four patients stopped treatment between three and six months; three of them had recurrences before one year and one had no evidence of disease at seven years. Seven patients completed the course; of these three had recurrences within six months, and three more had recurrences at 8 , 15, and 45 months, respectively.
Toxicity was nearly universal; cheilosis, conjunctivitis, pruritus, joint and eye pain, flashing lights, and erythrocyte sedimentation rate (ESR) over 60 were all noted. The lack of positive results and the frequency and severity of toxicity led to termination of the study. o 1992 Wey-Liss, Inc.
๐ SIMILAR VOLUMES
The pharmacokinetics of three 13-cis-retinoic acid formulations were studied after intraperitoneal (ip) administration to rats. Rats were given ip injections of 2.5 mg of 13-cis-retinoic acid per 360 g of body weight; the drug was administered as an alkaline solution, suspended in corn oil, or as a