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Selective estrogen receptor alpha agonist GTx-758 decreases testosterone with reduced side effects of androgen deprivation therapy in men with advanced prostate cancer

  • Evan Y. Yu
  • , Robert H. Getzenburg
  • , Christopher C. Coss
  • , Mark M. Gittelman
  • , Thomas Keane
  • , Ronald Tutrone
  • , Laurence Belkoff
  • , Robert Given
  • , Joel Bass
  • , et al.

Research output: Contribution to journalArticlepeer-review

Abstract

Background A need remains for new therapeutic approaches for men with advanced prostate cancer, particularly earlier in the disease course. Objective To assess the ability of an oral selective estrogen receptor a agonist (GTx-758) to lower testosterone concentrations compared with leuprolide while minimizing estrogen deficiency-related side effects of androgen-deprivation therapy. Design, setting, and participants Hormone-naive advanced prostate cancer patients were randomized to oral GTx-758 1000 mg/d, 2000 mg/d, or leuprolide depot. Intervention GTx-758 and leuprolide. Outcome measurements and statistical analysis The primary end point was the proportion of patients achieving total testosterone =50 ng/dl by day 60. Secondary end points included serum free testosterone, prostate-specific antigen (PSA), sex hormone-binding globulin, hot flashes, bone turnover markers, and insulin-like growth factor (IGF)-1 levels. Results and limitations Of 159 randomized patients, leuprolide reduced total testosterone to =50 ng/dl in a greater proportion of patients than GTx-758 by day 60 (43.4%, 63.6%, and 88.2% of subjects receiving GTx-758 1000 mg [p < 0.001], GTx-758 2000 mg [p = 0.004], and leuprolide, respectively). GTx-758 reduced free testosterone and PSA earlier and to a greater degree than leuprolide. GTx-758 led to fewer hot flashes, decreases in bone turnover markers, and alterations in IGF-1 compared with leuprolide. A higher incidence of venous thromboembolic events (VTEs) was seen with GTx-758 (4.1%) compared with leuprolide (0.0%). Conclusions Although leuprolide reduced total testosterone to =50 ng/dl in a greater proportion of patients compared with GTx-758, GTx-758 was superior in lowering free testosterone and PSA. GTx-758 reduced estrogen deficiency side effects of hot flashes, bone loss, and insulin resistance but with a higher incidence of VTEs. Patient summary This paper reports findings that leuprolide lowered total testosterone more than GTx-758 but that GTx-758 lowered free testosterone and prostate-specific antigen more than leuprolide. GTx-758 also reduced estrogen deficiency side effects, albeit at a higher rate of vascular events. Trial registration Clinicaltrials.gov identifier NCT01615120. © 2014 European Association of Urology. Published by Elsevier B.V. All rights reserved.

Original languageAmerican English
JournalEuropean urology
Volume67
StatePublished - Jan 1 2015

Keywords

  • Article
  • Bone turnover
  • Estrogen receptor
  • Free testosterone
  • GTx-758
  • Leuprolide
  • Prostate cancer
  • Sex hormone-binding globulin
  • advanced cancer
  • aged
  • alkaline phosphatase
  • androgen deprivation therapy
  • biological marker
  • cancer patient
  • deep vein thrombosis
  • drug dose comparison
  • drug withdrawal
  • estrogen deficiency
  • estrogen receptor alpha
  • gtx 758
  • heart arrest
  • hot flush
  • human
  • insulin resistance
  • leuprorelin
  • lung embolism
  • major clinical study
  • male
  • multicenter study
  • osteolysis
  • outcome assessment
  • phase 2 clinical trial
  • priority journal
  • prostate specific antigen
  • protein blood level
  • selective estrogen receptor modulator
  • sex hormone binding globulin
  • side effect
  • somatomedin C
  • testosterone
  • testosterone blood level
  • unclassified drug
  • venous thromboembolism

Disciplines

  • Urology

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