Pharmacokinetics, efficacy, and safety of a permeation-enhanced testosterone transdermal system in comparison with bi-weekly injections of testosterone enanthate for the treatment of hypogonadal men

被引:270
作者
Dobs, AS
Meikle, AW
Arver, S
Sanders, SW
Caramelli, KE
Mazer, NA
机构
[1] Johns Hopkins Med Ctr, Baltimore, MD 21287 USA
[2] Univ Utah, Dept Med, Salt Lake City, UT 84132 USA
[3] Univ Utah, Dept Pharmaceut, Salt Lake City, UT 84132 USA
[4] Karolinska Hosp, S-10401 Stockholm, Sweden
[5] Theratech Inc, Salt Lake City, UT 84108 USA
关键词
D O I
10.1210/jc.84.10.3469
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The pharmacokinetics, efficacy, and safety of the Androderm testosterone (T) transdermal system (TTD) and intramuscular T enanthate injections (IM) for the treatment of male hypogonadism were compared in a 24-week multicenter, randomized, parallel-group study. Sixty-six adult hypogonadal men (22-65 years of age) were withdrawn from prior IM treatment for 4-6 weeks and then randomly assigned to treatment with TTD (two 2.5-mg systems applied nightly) or IM (200 mg injected every 2 weeks); there were 33 patients per group. Twenty-six patients in the TTD group and 32 in the IM group completed the study. TTD treatment produced circadian variations in the levels of total T, bioavailable T, dihydrotestosterone, and estradiol within the normal physiological ranges. IM treatment produced supraphysiological levels of T, bioavailable T, and estradiol (but not dihydrotestosterone) for set-cat days after each injection. Mean morning sex hormone levels were within the normal range in greater proportions of TTD patients (range, 77-100%) than IM patients (range, 19-84%). Both treatments normalized LH levels in approximately 50% of patients with primary hypogonadism; however, LH levels were suppressed to the subnormal range in 31% of IM patients us. 0% of TTD patients. Both treatments maintained sexual function (assessed by questionnaire and Rigiscan) and mood (Beck Depression Inventory) at the prior treatment levels. Prostate-specific antigen levels, prostate volumes, and lipid and serum chemistry parameters were comparable in both treatment groups. Transient shin irritation from the patches was reported by 60% of the TTD patients, but caused only three patients (9%) to discontinue treatment. Ih I treatment produced local reactions in 33% of patients and was associated with significantly more abnormal hematocrit elevations (43.8% of patients) compared with TTD treatment (15.4% of patients). Gynecomastia resolved more frequently during TTD treatment (4 of 10 patients) than with IM treatment (1 of 9 patients). Although both treatments seem to be efficacious for replacing T in hypogonadal men, the more physiological sex hormone levels and profiles associated with TTD may offer possible advantages over IM in minimizing excessive stimulation of erythropoiesis, preventing/ ameliorating gynecomastia, and not over-suppressing gonadotropins.
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收藏
页码:3469 / 3478
页数:10
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