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Department of Pathology, RWTH, Pauwelsstrasse, 5100 Aachen, West Germany [R. K., F. H.], and Institute of Urology, University College London, St. Paul's Hospital, 24 Endell Street, London WC2H 9AE, England [W. E. A. J., J. R. W. M.]
The in vitro cytotoxicities of the four drugs most frequently used for intravesical chemotherapy (Adriamycin, epodyl, mitomycin C, Thiotepa) and epirubicin were compared using monolayers and multicellular tumor spheroids of the human bladder cancer cell line, MGH-U1. Adriamycin and epirubicin were most cytotoxic against monolayer cultures, whereas mitomycin C killed more cells in spheroids. Epodyl was least cytotoxic against both two- and three-dimensional cultures. Thiotepa was the only drug more cytotoxic to three- than two-dimensional cultures. Topographic analysis of bromodeoxyuridine-stained nuclei using image analysis indicated that Adriamycin selectively removed or killed superficial cells in multicellular tumor spheroids, but had little effect on DNA synthesis within the spheroids. In contrast, Thiotepa killed cells throughout the spheroids. These in vitro data appear to reflect clinical experience using intravesical chemotherapy to treat superficial bladder cancer.
1 Recipient of support from Boehringer Ingelheim Fonds fuer Grudlagenforschung, West Germany. To whom requests for reprints should be addressed.
Received 9/ 8/87. Revised 5/ 6/88. Revised 10/13/88. Accepted 11/30/88.
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