Yonsei Med J.  2014 Mar;55(2):310-315.

Is High-Dose Leuprorelin Acetate Effective and Safe in Asian Men with Prostate Cancer? An Open-Label, Non-Comparative, Multi-Center Clinical Trial

Affiliations
  • 1Department of Urology, Gangnam Severance Hospital, Yonsei University Health System, Seoul, Korea. chung646@yuhs.ac
  • 2Department of Urology, Samsung Medical Center, Sungkyunkwan University College of Medicine, Seoul, Korea.
  • 3Department of Urology, Seoul St. Mary's Hospital, The Catholic University of Korea College of Medicine, Seoul, Korea.
  • 4Department of Urology, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea.
  • 5Department of Urology, Severance Hospital, Yonsei University College of Medicine, Seoul, Korea.
  • 6Department of Urology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
  • 7Department of Urology, Chonnam National University Hospital, Chonnam National University College of Medicine, Gwangju, Korea.

Abstract

PURPOSE
Leuprorelin is a well known luteinizing hormone releasing hormone agonist. However, there are insufficient data on the efficacy and safety of high dose leuprorelin acetate, especially in Asian patients with prostate cancer. We aimed to investigate the safety and efficacy of leuprorelin acetate 22.5 mg administered at three-month intervals in patients with prostate cancer.
MATERIALS AND METHODS
In an open, prospective clinical trial enrolling 47 patients, we aimed to assess the efficacy and safety of leuprorelin acetate 22.5 mg in treating patients with histologically confirmed prostate cancer. The primary objective of this study was to evaluate the efficacy of the leuprorelin acetate 22.5 mg in producing and maintaining castration levels of testosterone over a 6-month follow-up period and to determine its safety profile.
RESULTS
All 42 patients achieved serum testosterone levels within the castration range by 4 weeks. A breakthrough response was observed in one of 36 patients by 8 weeks. However, this patient was medically castrated by 12 weeks. There were no significant prostate-specific antigen (PSA) or testosterone changes according to clinical stage or body mass index. Twenty adverse events (AEs) in 15 of 42 patients (35.7%) were observed during this study. The most common AEs were hot flushes (n=4, 20.0%) with mild intensity, pain (n=2, 10.0%), and infection (n=2, 10.0%). No patient withdrew from the study due to AEs.
CONCLUSION
Leuprorelin acetate 22.5 mg was shown to be effective and safe in Asian patients with prostate cancer, even though sexual function decreased.

Keyword

Prostate cancer; luteinizing hormone releasing hormone agonist; adverse events

MeSH Terms

Asian Continental Ancestry Group*
Body Mass Index
Castration
Follow-Up Studies
Gonadotropin-Releasing Hormone
Humans
Leuprolide*
Male
Methods
Prospective Studies
Prostate*
Prostate-Specific Antigen
Prostatic Neoplasms*
Testosterone
Gonadotropin-Releasing Hormone
Leuprolide
Prostate-Specific Antigen
Testosterone

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