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Preclinical antitumor activity of batracylin (NSC 320846)

โœ Scribed by Jacqueline Plowman; Kenneth D. Paull; Ghanem Atassi; Steadman D. Harrison; Donald J. Dykes; Hans J. Kabbe; V. L. Narayanan; Omar C. Yoder


Publisher
Springer US
Year
1988
Tongue
English
Weight
471 KB
Volume
6
Category
Article
ISSN
0167-6997

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โœฆ Synopsis


Batracylin (NSC 320846, BAY H 2049), given ip on days 2 and 9 at a dose of 400 mg/kg, inhibited tumor growth completely in 80-100~ of mice with early-stage colon adenocarcinoma 38. Therapeutic efficacy against this subcutaneously implanted tumor was retained upon oral administration of Batracylin although, compared to ip treatment, larger doses were required. Batracylin also caused regression of advanced (400 mg) colon 38 tumors. Only modest activity was observed for this compound against P388 leukemia, but P388 sublines with acquired resistance to either adriamycin or cisplatin demonstrated collateral sensitivity. Batracylin currently is undergoing toxicological evaluation by NCI prior to clinical trials.


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Activity of batracylin (NSC-320846) agai
โœ Patricia Mucci-LoRusso; Lisa Polin; Marie-Christine Bissery; Frederick Valeriote ๐Ÿ“‚ Article ๐Ÿ“… 1989 ๐Ÿ› Springer US ๐ŸŒ English โš– 882 KB

Batracylin (NSC 320846) is a water insoluble, solid tumor active compound discovered by the Development Therapeutics Program of the National Cancer Institute (NCI). In vivo, the NCI found this compound to be highly active [median treated tumor mass/median control tumor mass (T/C) = 0 to 20%] both or