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Entacapone and prostate cancer risk in patients with Parkinson's disease

Korhonen, Pasi (author)
EPID Research Oy, Espoo, Finland
Kuoppamäki, Mikko (author)
Orion Pharma, Orion Corporation, Espoo, Finland
Prami, Tuire (author)
EPID Research Oy, Espoo, Finland
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Hoti, Fabian (author)
EPID Research Oy, Espoo, Finland
Christopher, Solomon (author)
EPID Research Oy, Espoo, Finland
Ellmen, Juha (author)
Orion Pharma, Orion Corporation, Espoo, Finland
Aho, Valtteri (author)
Orion Pharma, Orion Corporation, Espoo, Finland
Vahteristo, Mikko (author)
Orion Pharma, Orion Corporation, Espoo, Finland
Pukkala, Eero (author)
Finnish Cancer Registry, Institute for Statistical and Epidemiological Cancer Research, Helsinki, Finland; School of Health Sciences, University of Tampere, Tampere, Finland
Haukka, Jari (author)
EPID Research Oy, Espoo, Finland
Tuvblad, Catherine, 1968- (contributor)
Örebro universitet,Institutionen för juridik, psykologi och socialt arbete,CAPS
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 (creator_code:org_t)
2015-01-16
2015
English.
In: Movement Disorders. - Hoboken, USA : Wiley-Blackwell. - 0885-3185 .- 1531-8257. ; 30:5, s. 724-728
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Background: The association between Parkinson’s disease (PD) and prostate cancer, both common in elderly men, is disputable. In the STRIDE-PD study, prostate cancer developed in 9 patients (3.7%) receiving levodopa/carbidopa with entacapone, a catechol-O-methyltransferase inhibitor, versus 2 cases (0.9%) without entacapone. The current pharmacoepidemiological study aimed to determine whether entacapone increases prostate cancer incidence or mortality in PD patients and whether cumulative exposure affects these rates.Methods: We performed a retrospective cohort study using population-wide health care registers with patientlevel linkage. Prostate cancer incidence and mortality were modeled by Cox’s proportional hazards models.Results and Conclusions: Use of entacapone with Ldopa/dopa decarboxylase inhibitor caused no increased risk of prostate cancer incidence (hazard ratio [HR]: 1.05; 95% confidence interval: 0.76-1.44) or mortality (0.93; 0.43-1.98). The HR for cumulative entacapone use of >360 days versus never-use was 0.82 (0.56-1.18) for prostate cancer incidence and 1.27 (0.60-2.72) for prostate cancer mortality.

Subject headings

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

Keyword

Entacapone
evodopa
prostate cancer
pharmacoepidemiology

Publication and Content Type

ref (subject category)
art (subject category)

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