Abstract | OBJECTIVES: METHODS: A total of 321 patients with metastatic prostate cancer in relapse after first-line endocrine therapy entered a Phase III international multicenter study (recruitment from February 1992 to August 1994) comparing liarozole (300 mg two times daily) with CPA (100 mg two times daily). RESULTS: Accounting for differences in baseline prognostic factors, the adjusted hazard ratio for survival was 0.74 in favor of liarozole (P = 0.039), indicating a 26% lower risk of death than in patients treated with CPA. Median crude (unadjusted) survival time was the same in the liarozole group as in the CPA group (10.3 months). More patients showed a PSA response (at least 50% reduction in PSA from baseline) when treated with liarozole (20%) than with CPA (4%) (P < 0.001). Prostate-specific antigen (PSA) responders had a median survival benefit of 10 months over nonresponders, irrespective of treatment (hazard ratio 0.43; P = 0.0018). PSA response was apparent within 3 months in approximately 90% of patients who responded. Pain improved more in the liarozole group than in the CPA group (P = 0.03). PSA responders had lower median pain scores than nonresponders (1.7 versus 2.5) and better quality of life (median Functional Living Index- Cancer score 108 versus 98) at end point, ie, treatment discontinuation, as well as throughout the treatment period. Among the most frequently occurring adverse events in the liarozole group were dry skin (51% of patients), pruritus (25%), rash (16%), nail disorders (16%), and hair loss (15%). These adverse events were generally mild to moderate in severity and did not affect the overall quality of life score. There were no detectable effects of either treatment on vital signs such as blood pressure, heart rate, electrocardiogram, and body weight. CONCLUSIONS:
Liarozole is superior to CPA in terms of PSA response, PSA progression, and survival, and is capable of maintaining patients' quality of life. The observed adverse events were mild to moderate in nature. These results show that liarozole is a possible treatment option after first-line endocrine therapy has failed.
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Authors | F J Debruyne, R Murray, Y Fradet, J E Johansson, C Tyrrell, F Boccardo, L Denis, J M Marberger, D Brune, J Rassweiler, T Vangeneugden, J Bruynseels, M Janssens, P De Porre |
Journal | Urology
(Urology)
Vol. 52
Issue 1
Pg. 72-81
(Jul 1998)
ISSN: 0090-4295 [Print] United States |
PMID | 9671874
(Publication Type: Clinical Trial, Clinical Trial, Phase III, Comparative Study, Journal Article, Multicenter Study, Randomized Controlled Trial)
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Chemical References |
- Androgen Antagonists
- Imidazoles
- Cyproterone Acetate
- Prostate-Specific Antigen
- liarozole
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Topics |
- Aged
- Aged, 80 and over
- Androgen Antagonists
(adverse effects, therapeutic use)
- Cyproterone Acetate
(adverse effects, therapeutic use)
- Disease Progression
- Humans
- Imidazoles
(adverse effects, therapeutic use)
- Male
- Middle Aged
- Neoplasm Metastasis
- Neoplasm Staging
- Prostate-Specific Antigen
(blood)
- Prostatic Neoplasms
(blood, drug therapy, mortality, pathology)
- Survival Rate
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