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Anti-androgen monotherapy versus gonadotropin-releasing hormone agonists in men with advanced, non-metastatic prostate cancer : a register-based, observational study

Thomsen, Frederik Birkebaek (author)
Univ Copenhagen, Rigshosp, Dept Urol, Copenhagen Prostate Canc Ctr, Ole Maaloes Vej 24,Afs 7521, DK-2200 Copenhagen, Denmark
Bosco, Cecilia (author)
Kings Coll London, TOUR, Sch Canc & Pharmaceut Sci, London, England
Garmo, Hans (author)
Kings Coll London, TOUR, Sch Canc & Pharmaceut Sci, London, England;Uppsala Univ Hosp, Reg Canc Ctr Uppsala Orebro, Uppsala, Sweden
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Adolfsson, Jan (author)
Karolinska Institutet
Hammar, Niklas (author)
Karolinska Institutet
Stattin, Pär (author)
Uppsala universitet,Urologkirurgi
Van Hemelrijck, Mieke (author)
Kings Coll London, TOUR, Sch Canc & Pharmaceut Sci, London, England;Karolinska Inst, Inst Environm Med, Unit Epidemiol, Stockholm, Sweden
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 (creator_code:org_t)
2019
2019
English.
In: Acta Oncologica. - 0284-186X .- 1651-226X. ; 58:1, s. 110-118
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Background:In randomised controlled trials, men with advanced, non-metastatic prostate cancer (PCa) treated with anti-androgen monotherapy (AA) had similar all-cause mortality as men treated with gonadotropin-releasing hormone (GnRH) agonists. Using real-world evidence (i.e., observational data), we aimed to further assess the difference in mortality between these two drug categories.Material and Methods:We emulated a trial using data from Prostate Cancer data Base Sweden 3.0. We specifically focused on men diagnosed in 2006-2012 with high-risk PCa who had no distant metastasis. They either received primary hormonal therapy with AA (n=2078) or GnRH agonists (n=4878) who were followed for a median time of 5 years. Risk of death from PCa and other causes was assessed using competing risk analyses and Cox proportional hazards regression analyses, including propensity score matching.Results:The cumulative 5-year PCa mortality was lower for men treated with AA (16% [95% confidence interval, CI, 15-18%]) than men treated with GnRH agonists (22% [95% CI 21-24%]). The 5-year other cause mortality was also lower for men on AA (17% [95% CI 15-19%] compared to men on GnRH agonists (27% [95% CI 25-28%]). In regression analyses, the risk of PCa death was similar, GnRH agonists versus AA (reference), hazard ratio (HR) 1.08 (95% CI 0.95-1.23), but the risk of death from all causes was higher for men on GnRH agonists, HR 1.23 (95% CI 1.13-1.34). Consistent results were seen in the propensity score-matched cohort.Conclusion:Our results indicate that the use of AA as primary hormonal therapy in men with high-risk non-metastatic PCa does not increase PCa-specific mortality compared to GnRH. Using AA instead of GnRH agonists may result in shorter time on/exposure to GnRH-treatment, which may reduce the risk of adverse events associated with this treatment.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Urologi och njurmedicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Urology and Nephrology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Endokrinologi och diabetes (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Endocrinology and Diabetes (hsv//eng)

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