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Association between PSA kinetics and cancer-specific mortality in patients with localised prostate cancer : analysis of the placebo arm of the SPCG-6 study

Thomsen, F. B. (author)
Copenhagen Prostate Cancer Center, Department of Urology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark
Brasso, K. (author)
Copenhagen Prostate Cancer Center, Department of Urology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark
Berg, K. D. (author)
Copenhagen Prostate Cancer Center, Department of Urology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark
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Gerds, T. A. (author)
Department of Biostatistics, University of Copenhagen, Copenhagen, Denmark
Johansson, J-E, 1956- (author)
Örebro universitet,Institutionen för hälsovetenskap och medicin,Department of Urology, Faculty of Medicine and Health
Angelsen, A. (author)
Faculty of Medicine, Norwegian University of Technology and Science, Trondheim, Norway
Tammela, T. L. J. (author)
Department of Surgery, Tampere University Hospital and School of Medicine, University of Tampere, Tampere, Finland
Iversen, P. (author)
Copenhagen Prostate Cancer Center, Department of Urology, Rigshospitalet, University of Copenhagen, Copenhagen, Denmark
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 (creator_code:org_t)
Oxford, United Kingdom : Oxford University Press, 2016
2016
English.
In: Annals of Oncology. - Oxford, United Kingdom : Oxford University Press. - 0923-7534 .- 1569-8041. ; 27:3, s. 460-466
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Background: The prognostic value of prostate-specific antigen (PSA) kinetics in untreated prostate cancer (PCa) patients is debatable. We investigated the association between PSA doubling time (PSAdt), PSA velocity (PSAvel) and PSAvel risk count (PSAvRC) and PCa mortality in a cohort of patients with localised PCa managed on watchful waiting.Patients and methods: Patients with clinically localised PCa managed observationally, who were randomised to and remained on placebo for minimum 18 months in the SPCG-6 study, were included. All patients survived at least 2 years and had a minimum of three PSA determinations available. The prognostic value of PSA kinetics was analysed and patients were stratified according to their PSA at consent: ≤10, 10.1-25, and >25 ng/ml. Cumulative incidences of PCa-specific mortality were estimated with the Aalen-Johansen method.Results: Two hundred and sixty-three patients were included of which 116, 76 and 71 had a PSA at consent ≤10, 10.1-25, and >25 ng/ml, respectively. Median follow-up was 13.6 years. For patients with PSA at consent between 10.1 and 25 ng/ml, the 13-year risks of PCa mortality were associated with PSA kinetics: PSAdt ≤3 years: 62.0% versus PSAdt >3 years: 16.3% (Gray's test: P < 0.0001), PSAvel ≥2 ng/ml/year: 48.0% versus PSAvel <2 ng/ml/year: 11.0% (Gray's test: P = 0.0008), and PSAvRC 2: 45.0% versus 0-1: 3.8% (Gray's test: P = 0.001). In contrast, none of the PSA kinetics were significantly associated with changes of 13-year risks of PCa mortality in patients with PSA at consent ≤10 or >25 ng/ml.Conclusion: We found that magnitude changes in 13-year risks of PCa mortality that can be indicated by PSA kinetics depend on PSA level in patients with localised PCa who were managed observationally. Our results question PSA kinetics as surrogate marker for PCa mortality in patients with low and high PSA values.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)

Keyword

Prostate cancer
survival
PSA kinetic
PSA doubling time
PSA velocity
PSA velocity risk count
Onkologi
Oncology

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art (subject category)

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