TY - JOUR
T1 - The Effect of Nafarelin Acetate, a Luteinizing-Hormone–Releasing Hormone Agonist, on Benign Prostatic Hyperplasia
AU - Peters, Craig A.
AU - Walsh, Patrick C.
PY - 1987/9/3
Y1 - 1987/9/3
N2 - We examined the influence of androgens on benign prostatic hyperplasia, using nafarelin acetate, a potent luteinizing-hormone–releasing hormone agonist, to achieve reversible androgen deprivation in men with benign prostatic hyperplasia. Nine patients with bladder-outlet obstruction due to benign prostatic hyperplasia were treated with subcutaneous nafarelin acetate (400 μg per day) in an open trial for six months. In all patients, serum testosterone decreased to castrate levels. Objective observations included uroflowmetry, measurement of residual urine volume, determination of prostatic size by ultrasonography, and prostatic biopsy. In all patients, the prostate regressed to a mean (±SEM) of 75.8±3 percent of the initial size (range, 52 to 86; P<0.005); the regression reached a plateau after four months. Morphologic analysis of biopsy specimens showed regression of glandular epithelium. Three of nine patients had clinical improvement with treatment. Six months after the cessation of treatment, plasma testosterone levels had returned to normal and the size of the prostate had increased to 99±5.5 percent of the initial size. These findings suggest that androgens have an important supportive role in established benign prostatic hyperplasia and that testicular suppression will benefit some patients. However, this form of treatment could be applicable only in carefully selected patients who were not surgical candidates, and it would need to be maintained indefinitely. (N Engl J Med 1987; 317:599–604.), BENIGN prostatic hyperplasia is the most common benign neoplasm in men, producing symptoms of urinary-outlet obstruction in 75 percent of men over 50 years of age; more than 350,000 prostatectomies are performed each year.1 Although the disorder is almost universal among aging men, its pathogenesis is poorly understood, and consequently, no effective nonsurgical approaches to treatment are available. Two important factors appear necessary for the induction of benign prostatic hyperplasia in men: the testes and aging. Benign prostatic hyperplasia is not known to occur in patients castrated before the age of 40 years,1 yet it is unclear whether the testes…
AB - We examined the influence of androgens on benign prostatic hyperplasia, using nafarelin acetate, a potent luteinizing-hormone–releasing hormone agonist, to achieve reversible androgen deprivation in men with benign prostatic hyperplasia. Nine patients with bladder-outlet obstruction due to benign prostatic hyperplasia were treated with subcutaneous nafarelin acetate (400 μg per day) in an open trial for six months. In all patients, serum testosterone decreased to castrate levels. Objective observations included uroflowmetry, measurement of residual urine volume, determination of prostatic size by ultrasonography, and prostatic biopsy. In all patients, the prostate regressed to a mean (±SEM) of 75.8±3 percent of the initial size (range, 52 to 86; P<0.005); the regression reached a plateau after four months. Morphologic analysis of biopsy specimens showed regression of glandular epithelium. Three of nine patients had clinical improvement with treatment. Six months after the cessation of treatment, plasma testosterone levels had returned to normal and the size of the prostate had increased to 99±5.5 percent of the initial size. These findings suggest that androgens have an important supportive role in established benign prostatic hyperplasia and that testicular suppression will benefit some patients. However, this form of treatment could be applicable only in carefully selected patients who were not surgical candidates, and it would need to be maintained indefinitely. (N Engl J Med 1987; 317:599–604.), BENIGN prostatic hyperplasia is the most common benign neoplasm in men, producing symptoms of urinary-outlet obstruction in 75 percent of men over 50 years of age; more than 350,000 prostatectomies are performed each year.1 Although the disorder is almost universal among aging men, its pathogenesis is poorly understood, and consequently, no effective nonsurgical approaches to treatment are available. Two important factors appear necessary for the induction of benign prostatic hyperplasia in men: the testes and aging. Benign prostatic hyperplasia is not known to occur in patients castrated before the age of 40 years,1 yet it is unclear whether the testes…
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U2 - 10.1056/NEJM198709033171004
DO - 10.1056/NEJM198709033171004
M3 - Article
C2 - 2441256
AN - SCOPUS:0023227737
SN - 0028-4793
VL - 317
SP - 599
EP - 604
JO - New England Journal of Medicine
JF - New England Journal of Medicine
IS - 10
ER -