SFEBES2007 Poster Presentations Reproduction (13 abstracts)
Royal Victoria Infirmary, Newcastle upon Tyne, United Kingdom.
Conventional intramuscular preparations of testosterone esters are associated with wide fluctuations in serum testosterone (T) levels following administration, even when a lower dose (100 mg) is injected every 710 days, let alone 250 mg every 23 weeks. Depot Testosterone undecanoate [TU -Nebido] is a newly available option for androgen replacement. The possibility of achieving stable therapeutic serum T levels over a period of months is its principal attraction. Data from Germany suggest that, after adequate loading, patients can be maintained on injections spaced >12 weeks apart.
We report our initial experience with use of TU in a cohort of 20 men with organic severe hypogonadism (eg. hypopituitary, Kallmanns, Klinefelters, or survivors of childhood cancer baseline 9 am serum T at original diagnosis 05.0 nmol/L), who received TU injections for up to 9 months. All were transferred from other forms of T replacement and treatment was initiated with two injections of TU 1000 mg given 6-weeks apart (loading dose), followed by 1000 mg initially every 12 weeks. Following the first injection, serum T levels were measured prior to their next loading injection at 6 weeks and before every subsequent injection.
The medication was well-tolerated and no significant local irritation was reported. Individual dosing intervals ranged from 1214 weeks. Serum total T levels prior to the second loading dose at 6 weeks was 14.4±1.4 nmol/L and serum free T levels were 261±21.5 pmol/L. Serum total T levels prior to the 3rd injection was 19.5±1.8 nmol/L, with serum free T levels 354±58.8 pmol/L. Dosing intervals were increased as appropriate and T levels prior to subsequent injections were all within the normal range, indicating physiological T replacement. All patients reported high levels of satisfaction, confirming that TU (Nebido) is a useful and well-tolerated form of replacement therapy even in men with near-total deficiency of endogenous T secretion.