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Curr Urol. 2021 Mar;15(1):63-67. doi: 10.1097/CU9.0000000000000008. Epub 2021 Mar 29.

A prospective study of the effect of testosterone escape on preradiotherapy prostate-specific antigen kinetics in prostate cancer patients undergoing neoadjuvant androgen deprivation therapy.

Current urology

David R H Christie, Natalia Mitina, Christopher F Sharpley

Affiliations

  1. Genesiscare, Inland Drive, Tugun, Queensland, Australia.
  2. Brain-Behaviour Research Group, University of New England, Armidale, Australia.
  3. University of Queensland, St Lucia, Queensland, Australia.

PMID: 34084124 PMCID: PMC8137000 DOI: 10.1097/CU9.0000000000000008

Abstract

INTRODUCTION: Prostate-specific antigen (PSA) kinetic patterns during neoadjuvant androgen deprivation therapy have been shown to predict unfavorable long-term outcomes.

OBJECTIVE: To investigate the effect of testosterone escape (TE) on these kinetic patterns, as this had not been previously reported.

METHODS: There were 50 consecutive prostate cancer patients who received 6 months of triptorelin prior to definitive radiotherapy (RT). Testosterone and PSA levels were measured at baseline and every 6 weeks. Clinical factors were tested for their ability to predict for TE and unfavorable PSA kinetic patterns. The effects of TE, at both 1.7 and 0.7 nmol/L levels, were analyzed.

RESULTS: TE occurred in at least one reading for 14% and 34% of the patients at the 1.7 and 0.7 nmol/L levels, respectively. No baseline factors predicted TE. The median PSA halving time was 25 days and the median pre-RT PSA level was 0.55 ng/mL. The only factor significantly associated with a higher pre-RT PSA level was a higher baseline PSA level. The only factor that significantly predicted a longer PSA halving time was TE at the 1.7 nmol/L level.

CONCLUSIONS: TE and higher baseline PSA levels may adversely affect PSA kinetics and other outcomes for patients undergoing neoadjuvant hormone therapy prior to radiotherapy. Studies investigating the tailoring of neoadjuvant therapy by extending the duration in those patients with a higher baseline PSA level or by the addition of anti-androgens in those demonstrating TE, should be considered.

Copyright © 2021 The Authors. Published by Wolters Kluwer Health, Inc.

Keywords: Gonadotropin-releasing hormone; Prostate-specific antigen; Prostatic neoplasm; Radiotherapy; Testosterone

Conflict of interest statement

The authors declare that they have no financial conflict of interest with regard to the content of this report.

References

  1. Pharmacotherapy. 2018 Mar;38(3):327-333 - PubMed
  2. J Clin Oncol. 2007 Jan 1;25(1):77-84 - PubMed
  3. Prostate Cancer Prostatic Dis. 2019 Mar;22(1):24-38 - PubMed
  4. Int J Radiat Oncol Biol Phys. 2011 Dec 1;81(5):e713-9 - PubMed
  5. Prostate Cancer. 2019 Mar 3;2019:6932572 - PubMed
  6. Rev Urol. 2018;20(2):63-68 - PubMed
  7. F1000Res. 2018 Feb 28;7:246 - PubMed
  8. Urol Oncol. 2014 Jan;32(1):38.e17-28 - PubMed
  9. J Urol. 2007 Oct;178(4 Pt 1):1290-5 - PubMed
  10. BJU Int. 2012 Dec;110(11 Pt B):E500-7 - PubMed
  11. BJU Int. 2018 Sep;122(3):371-383 - PubMed
  12. Can Urol Assoc J. 2013 May-Jun;7(5-6):E263-7 - PubMed
  13. Int J Radiat Oncol Biol Phys. 2011 Mar 15;79(4):1022-8 - PubMed
  14. Cancer Treat Rev. 2016 May;46:35-41 - PubMed
  15. Clin Genitourin Cancer. 2018 Apr;16(2):e491-e496 - PubMed
  16. Prostate Cancer Prostatic Dis. 2013 Dec;16(4):346-51 - PubMed
  17. Radiat Oncol. 2012 Dec 10;7:209 - PubMed
  18. BMC Cancer. 2010 Dec 09;10:675 - PubMed
  19. Urol Oncol. 2014 Jul;32(5):687-93 - PubMed
  20. Int J Radiat Oncol Biol Phys. 2010 Jan 1;76(1):23-30 - PubMed
  21. J Clin Oncol. 2015 Apr 1;33(10):1151-6 - PubMed
  22. Can Urol Assoc J. 2018 Feb;12(2):30-37 - PubMed
  23. Int J Radiat Oncol Biol Phys. 2013 Feb 1;85(2):385-92 - PubMed

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