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Six-month depot formulation of leuprorelin acetate in the treatment of prostate cancer
Author(s) -
Nicholas J Sanfilippo,
Sethi
Publication year - 2009
Publication title -
clinical interventions in aging
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.184
H-Index - 76
eISSN - 1178-1998
pISSN - 1176-9092
DOI - 10.2147/cia.s4885
Subject(s) - leuprorelin , medicine , tolerability , prostate cancer , androgen deprivation therapy , adjuvant , depot , oncology , bicalutamide , hormone , cancer , gonadotropin releasing hormone , urology , gynecology , luteinizing hormone , adverse effect , androgen receptor , archaeology , history
Hormonal deprivation therapy is well established for the treatment of locally advanced and metastatic prostate cancer, as well as the adjuvant treatment of some patients with localized disease. Long-acting gonadotropin releasing hormone (GnRH) agonists have become a mainstay of androgen deprivation therapy, due to their efficacy, tolerability, and convenience of use. One-month, 3-month, and 4-month depot leuprorelin formulations are well established and widely used to this end. Recently, a 6-month depot leuprorelin has been approved for use in advanced and metastatic prostate cancer patients. With similar efficacy and side effect profiles to earlier formulations, 6-month depot leuprorelin is a convenient treatment option for these patients. This review will highlight the role of GnRH agonists in the treatment of prostate cancer with a focus on the clinical efficacy, pharmacology, and patient-focused outcomes of the newer 6-month 45 mg depot leuprorelin formulation in comparison to available shorter-acting products.

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