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KMID : 1011820180590010018
Investigative and Clinical Urology
2018 Volume.59 No. 1 p.18 ~ p.24
Factors associated with testosterone recovery after androgen deprivation therapy in patients with prostate cancer
Nam Wook

Choi Se-Young
Yoo Sang-Jun
Ryu Je-Man
Lee Jae-Hoon
Kyung Yoon-Soo
Han Jae-Hyeon
You Dal-San
Jeong In-Gab
Hong Jun-Hyuk
Ahn Han-Jong
Kim Choung-Soo
Abstract
Purpose: We investigated factors affecting testosterone recovery after androgen deprivation therapy (ADT) withdrawal in patients with prostate cancer.

Materials and Methods: The medical records of patients who underwent radical prostatectomy with ADT were retrospectively reviewed. In all, 221 patients were included in the analysis. Testosterone recovery was defined as supra-castration (SC) (testosterone levels in serum >50 ng/dL) or out of hypogonadism (OH) (>300 ng/dL) after ADT withdrawal. Kaplan-Meier analyses were used to estimate testosterone recovery after ADT cessation. Cox regression analyses were used to determine the factors affecting the recovery of testosterone.

Results: After ADT, 206 patients (93.2%) recovered to the SC level and 122 patients (55.2%) recovered to the OH level. Patients treated with ADT for ¡Â18 months recovered to OH in a mean of 6.8 months (74.6%), but patients treated with ADT for >18 months recovered in a mean of 9.7 months (27.5%). In multivariate analyses, age (hazard ratio [HR], 0.915; p<0.001), serum level of sex hormone-binding globulin (SHBG) (HR, 1.015; p=0.002), initial testosterone level (HR, 1.002; p=0.002), and ADT duration (HR, 0.915; p<0.001) were associated with recovery to the OH level after ADT withdrawal, and hypertension (HR, 0.697; p=0.029) and duration of ADT (HR, 0.979; p=0.012) were significantly associated with recovery to SC.

Conclusions: In patients treated with ADT for ¡Â18 months, testosterone recovers to the OH level more often and faster after ADT cessation. Age, SHBG level, initial testosterone level, and ADT duration are associated with testosterone recovery.
KEYWORD
Androgen deprivation therapy, Prostatic neoplasms, Testosterone
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