| Literature DB >> 3103904 |
C A Presant, M S Soloway, S S Klioze, A Yakabow, S N Presant, R G Mendez, P S Kennedy, M R Wyres, V L Naessig, B Todd.
Abstract
The safety and efficacy of buserelin, a luteinizing hormone-releasing hormone (LH-RH) agonist, was tested in 33 evaluable patients with Stages C or D adenocarcinoma of the prostate. With a minimum follow-up duration of 10 months, there was one complete response and 22 partial responses (69%) by National Prostatic Cancer Project criteria, with a median duration greater than 18 months. Six patients (18%) had stable disease, median duration greater than 25 months, and only 12 patients have progressed. Performance status improved in 67%, patient-scored pain improved in 75%, and quality of life improved in 58%. Symptoms occurring during treatment consisted of hot flashes, loss of libido, and impotence. Buserelin produces a high frequency of durable objective and subjective responses in patients with advanced prostatic carcinoma.Entities:
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Year: 1987 PMID: 3103904 DOI: 10.1002/1097-0142(19870515)59:10<1713::aid-cncr2820591006>3.0.co;2-8
Source DB: PubMed Journal: Cancer ISSN: 0008-543X Impact factor: 6.860