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Leuprorelin acetate blood levels and dialysance after the administration of sustained-release leuprorelin acetate in a dialysis case complicated by prostate cancer

BACKGROUND The objective of this study is to determine whether in a dialysis patient with prostate cancer leuprorelin acetate blood levels were abnormally high or low due to kidney failure or because of dialysis. METHODS Sustained‐release leuprorelin acetate 3.75 mg was given every 4 weeks for prost...

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Published in:The Prostate 1998-02, Vol.34 (3), p.191-194
Main Authors: Saruki, Kazuhisa, Sekihara, Tetsuo, Mashimo, Masamichi, Matsuo, Hidenori, Sekiguchi, Hiroyuki
Format: Article
Language:English
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Summary:BACKGROUND The objective of this study is to determine whether in a dialysis patient with prostate cancer leuprorelin acetate blood levels were abnormally high or low due to kidney failure or because of dialysis. METHODS Sustained‐release leuprorelin acetate 3.75 mg was given every 4 weeks for prostate cancer in a 79‐year‐old dialysis patient. Changes in serum level of leuprorelin acetate in this patient were measured before and after dialysis. RESULTS Leuprorelin acetate appeared to have a dialysance close to that of vitamin B12, which has a similar molecular weight. The amount dialyzed did not exceed 8.3% of the amount released per day. Mean blood levels of leuprorelin acetate, as measured in this patient, were higher (0.64 to 1.31 ng/ml) than those in prostate cancer patients with normal kidney function (mean ± SD, 0.24 ± 0.12 to 0.50 ± 0.32 ng/ml). CONCLUSIONS Sustained‐release leuprorelin acetate can be used safely in dialysis patients with prostate cancer. Prostate 34:191–194, 1998. © 1998 Wiley‐Liss, Inc.
ISSN:0270-4137
1097-0045
DOI:10.1002/(SICI)1097-0045(19980215)34:3<191::AID-PROS6>3.0.CO;2-L