Time course of serum testosterone and luteinizing hormone levels after cessation of long-term luteinizing hormone-releasing hormone agonist treatment in patients with prostate cancer
Introduction In order to elucidate the influence of hormone‐releasing hormone (LH‐RH) agonist therapy cessation on pituitary/testicular function and its clinical implications, we investigated prospectively hormonal (luteinizing hormone: LH; testosterone: T) responses in patients with prostate cancer...
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Veröffentlicht in: | The Prostate 2006-03, Vol.66 (4), p.439-444 |
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Zusammenfassung: | Introduction
In order to elucidate the influence of hormone‐releasing hormone (LH‐RH) agonist therapy cessation on pituitary/testicular function and its clinical implications, we investigated prospectively hormonal (luteinizing hormone: LH; testosterone: T) responses in patients with prostate cancer who received long‐term LH‐RH 10 agonist therapy.
Patients and Methods
A consecutive 32 patients who had received LH‐RH agonist therapy over 24 months were enrolled. As a baseline, T and LH were measured at the time of LH‐RH agonist therapy cessation, monthly for 3 months, and subsequently, every 3 months.
Results
The median duration of LH‐RH agonist therapy was 30 months (24–87 months) with median follow‐up duration of 24 months following cessation. All patients had castrated T levels and suppressed LH levels at baseline. Median duration of castrated T levels following cessation was 6 months. Median time to normalization of T levels was 24 months. LH levels returned to normal within 3 months in all cases. Patients who received androgen deprivation therapy for 30 months or longer required a longer time for recovery of T levels. Patients over 65 years of age showed a statistically significant longer time for recovery of T levels (P = 0.0167).
Conclusions
Long‐term LH‐RH agonist therapy has remarkable effects on serum T level that last for a significant time after cessation, a fact that should be applied to the interpretation of both PSA and serum T levels after cessation of androgen deprivation therapy. © 2005 Wiley‐Liss, Inc. |
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ISSN: | 0270-4137 1097-0045 |
DOI: | 10.1002/pros.20341 |