Fracture after androgen deprivation therapy among men with a high baseline risk of skeletal complications

Yu Hsuan Shao, Dirk F. Moore, Weichung Shih, Yong Lin, Thomas L. Jang, Grace L. Lu-Yao

Research output: Contribution to journalArticle

31 Citations (Scopus)

Abstract

Objective To quantify the impact of androgen deprivation therapy (ADT) in men with a high baseline risk of skeletal complications and evaluate the risk of mortality after a fracture. Patients and Methods We studied 75 994 men, aged ≥66 years, with localized prostate cancer from the Surveillance, Epidemiology and End Results-Medicare linked data. Cox proportional hazard models were employed to evaluate the risk. Results Men with a high baseline risk of skeletal complications have a higher probability of receiving ADT than those with a low risk (52.1% vs 38.2%, P <0.001). During the 12-year follow-up, more than 58% of men with a high risk and 38% of men with a low risk developed at least one fracture after ADT. The dose effect of ADT is stronger among men who received ADT only compared to those who received ADT with other treatments. In the high-risk group, the fracture rate increased by 19.9 per 1000 person-years (from 52.9 to 73.0 person-years) for men who did not receive ADT compared to those who received 18 or more doses of gonadotropin-releasing hormone agonist among men who received ADT only, and by 14.2 per 1000 person-years (from 45.2 to 59.4 person-years) among men who received ADT and other treatments. Men experiencing a fracture had a 1.38-fold higher overall mortality risk than those who did not (95% CI, 1.34-1.43). Conclusions Men with a high baseline risk of skeletal complications developed more fractures after ADT. The mortality risk is 40% higher after experiencing a fracture. Consideration of patient risk before prescribing ADT for long-term use may reduce both fracture risk and fracture-associated mortality.

Original languageEnglish
Pages (from-to)745-752
Number of pages8
JournalBJU International
Volume111
Issue number5
DOIs
Publication statusPublished - May 2013
Externally publishedYes

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Androgens
Therapeutics
Mortality
Medicare
Proportional Hazards Models
Gonadotropin-Releasing Hormone
Prostatic Neoplasms
Epidemiology

Keywords

  • ADT
  • baseline risk
  • fracture
  • prostate cancer

ASJC Scopus subject areas

  • Urology

Cite this

Fracture after androgen deprivation therapy among men with a high baseline risk of skeletal complications. / Shao, Yu Hsuan; Moore, Dirk F.; Shih, Weichung; Lin, Yong; Jang, Thomas L.; Lu-Yao, Grace L.

In: BJU International, Vol. 111, No. 5, 05.2013, p. 745-752.

Research output: Contribution to journalArticle

Shao, Yu Hsuan ; Moore, Dirk F. ; Shih, Weichung ; Lin, Yong ; Jang, Thomas L. ; Lu-Yao, Grace L. / Fracture after androgen deprivation therapy among men with a high baseline risk of skeletal complications. In: BJU International. 2013 ; Vol. 111, No. 5. pp. 745-752.
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abstract = "Objective To quantify the impact of androgen deprivation therapy (ADT) in men with a high baseline risk of skeletal complications and evaluate the risk of mortality after a fracture. Patients and Methods We studied 75 994 men, aged ≥66 years, with localized prostate cancer from the Surveillance, Epidemiology and End Results-Medicare linked data. Cox proportional hazard models were employed to evaluate the risk. Results Men with a high baseline risk of skeletal complications have a higher probability of receiving ADT than those with a low risk (52.1{\%} vs 38.2{\%}, P <0.001). During the 12-year follow-up, more than 58{\%} of men with a high risk and 38{\%} of men with a low risk developed at least one fracture after ADT. The dose effect of ADT is stronger among men who received ADT only compared to those who received ADT with other treatments. In the high-risk group, the fracture rate increased by 19.9 per 1000 person-years (from 52.9 to 73.0 person-years) for men who did not receive ADT compared to those who received 18 or more doses of gonadotropin-releasing hormone agonist among men who received ADT only, and by 14.2 per 1000 person-years (from 45.2 to 59.4 person-years) among men who received ADT and other treatments. Men experiencing a fracture had a 1.38-fold higher overall mortality risk than those who did not (95{\%} CI, 1.34-1.43). Conclusions Men with a high baseline risk of skeletal complications developed more fractures after ADT. The mortality risk is 40{\%} higher after experiencing a fracture. Consideration of patient risk before prescribing ADT for long-term use may reduce both fracture risk and fracture-associated mortality.",
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AB - Objective To quantify the impact of androgen deprivation therapy (ADT) in men with a high baseline risk of skeletal complications and evaluate the risk of mortality after a fracture. Patients and Methods We studied 75 994 men, aged ≥66 years, with localized prostate cancer from the Surveillance, Epidemiology and End Results-Medicare linked data. Cox proportional hazard models were employed to evaluate the risk. Results Men with a high baseline risk of skeletal complications have a higher probability of receiving ADT than those with a low risk (52.1% vs 38.2%, P <0.001). During the 12-year follow-up, more than 58% of men with a high risk and 38% of men with a low risk developed at least one fracture after ADT. The dose effect of ADT is stronger among men who received ADT only compared to those who received ADT with other treatments. In the high-risk group, the fracture rate increased by 19.9 per 1000 person-years (from 52.9 to 73.0 person-years) for men who did not receive ADT compared to those who received 18 or more doses of gonadotropin-releasing hormone agonist among men who received ADT only, and by 14.2 per 1000 person-years (from 45.2 to 59.4 person-years) among men who received ADT and other treatments. Men experiencing a fracture had a 1.38-fold higher overall mortality risk than those who did not (95% CI, 1.34-1.43). Conclusions Men with a high baseline risk of skeletal complications developed more fractures after ADT. The mortality risk is 40% higher after experiencing a fracture. Consideration of patient risk before prescribing ADT for long-term use may reduce both fracture risk and fracture-associated mortality.

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