Literature DB >> 16809259

Individual variation of hormonal recovery after cessation of luteinizing hormone-releasing hormone agonist therapy in men receiving long-term medical castration therapy for prostate cancer.

Takashi Kobayashi1, Koji Nishizawa, Kenji Mitsumori.   

Abstract

OBJECTIVE: To evaluate the process of hormonal recovery after cessation of luteinizing hormone-releasing hormone (LHRH) agonist treatment in patients who had received long-term LHRH agonist therapy for prostate cancer.
MATERIAL AND METHODS: Men who had successfully undergone androgen deprivation therapy with only monthly LHRH agonist therapy for > 30 months were enrolled and the administration of LHRH agonist was discontinued. Serum total testosterone, luteinizing hormone (LH), follicle-stimulating hormone (FSH) and prostate-specific antigen (PSA) were measured before the cessation of LHRH agonist therapy and every 4 weeks thereafter, and the administration of LHRH agonist remained suspended until the total testosterone level recovered to > 50 ng/dl.
RESULTS: Ten patients were enrolled in the study. The median (range) castration period and the levels of serum LH, FSH, total testosterone and PSA at cessation of therapy were 39 (30-56) months,<0.5 (<0.5-1.8) mIU/ml, 6.4 (3.0-15.9) mIU/ml, 15.3 (5.8-34.7) ng/dl and 0.13 (0.02-0.89) ng/ml, respectively. Testosterone recovered to > 50 ng/dl in all cases. There were large variations in the times required for recovery of LH and FSH (30-100 days) and serum testosterone (30-330 days). PSA began to increase at various testosterone levels, and there was a large variation (0-83%; median 41%) in the ratio of the androgen suppression (testosterone < 50 ng/dl) time to the period of LHRH agonist cessation.
CONCLUSIONS: There was considerable variation in the hypothalamus-pituitary-testicular hormone profiles during recovery from long-term medical castration. These findings are noteworthy when interruption of androgen deprivation therapy is applied with the intention of delaying the progression of hormone-refractory cancer or improving the patient's quality of life.

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Year:  2006        PMID: 16809259     DOI: 10.1080/00365590600641533

Source DB:  PubMed          Journal:  Scand J Urol Nephrol        ISSN: 0036-5599


  3 in total

1.  Testosterone Recovery Profiles After Cessation of Androgen Deprivation Therapy for Prostate Cancer.

Authors:  Bruno Nascimento; Eduardo P Miranda; Lawrence C Jenkins; Nicole Benfante; Elizabeth A Schofield; John P Mulhall
Journal:  J Sex Med       Date:  2019-05-09       Impact factor: 3.802

2.  Abiraterone acetate plus LHRH therapy versus abiraterone acetate while sparing LHRH therapy in patients with progressive, metastatic and chemotherapy-naïve, castration-resistant prostate cancer (SPARE): study protocol for a randomized controlled trial.

Authors:  Carsten-Henning Ohlmann; Michelle Jäschke; Peter Jaehnig; Susane Krege; Jürgen Gschwend; Heidrun Rexer; Michael Stöckle
Journal:  Trials       Date:  2017-10-04       Impact factor: 2.279

3.  Enzalutamide in chemotherapy-naive patients with metastatic castration-resistant prostate cancer: A retrospective Korean multicenter study in a real-world setting.

Authors:  Seung Il Jung; Myung Soo Kim; Chang Wook Jeong; Cheol Kwak; Sung Kyu Hong; Seok Ho Kang; Jae Young Joung; Seung Hwan Lee; Seok Joong Yun; Tae-Hwan Kim; Sung Woo Park; Seong Soo Jeon; Minyong Kang; Ji Youl Lee; Byung Ha Chung; Jun Hyuk Hong; Hanjong Ahn; Choung-Soo Kim; Dong Deuk Kwon
Journal:  Investig Clin Urol       Date:  2019-12-10
  3 in total

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