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Sökning: onr:"swepub:oai:DiVA.org:oru-3669" > Testing a multigene...

Testing a multigene signature of prostate cancer death in the Swedish Watchful Waiting Cohort

Mucci, Lorelei A. (författare)
Pawitan, Yudi (författare)
Karolinska Institutet
Demichelis, Francesca (författare)
visa fler...
Fall, Katja (författare)
Karolinska Institutet
Stark, Jennifer R. (författare)
Adami, Hans-Olov (författare)
Karolinska Institutet
Andersson, Swen-Olof (författare)
Örebro universitet,Hälsoakademin
Andrén, Ove (författare)
Eisenstein, Anna (författare)
Holmberg, Lars (författare)
Uppsala universitet,Endokrinkirurgi
Huang, Wei (författare)
Kantoff, Philip W. (författare)
Kim, Robert (författare)
Perner, Sven (författare)
Stampfer, Meir J. (författare)
Johansson, Jan-Erik (författare)
Örebro universitet,Hälsoakademin
Rubin, Mark A. (författare)
visa färre...
 (creator_code:org_t)
Philadelphia : American Association for Cancer Research, 2008
2008
Engelska.
Ingår i: Cancer Epidemiology, Biomarkers and Prevention. - Philadelphia : American Association for Cancer Research. - 1055-9965 .- 1538-7755. ; 17:7, s. 1682-1688
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Although prostate cancer is a leading cause of cancer death, most men die with and not from their disease, underscoring the urgency to distinguish potentially lethal from indolent prostate cancer. We tested the prognostic value of a previously identified multigene signature of prostate cancer progression to predict cancer-specific death. The Örebro Watchful Waiting Cohort included 172 men with localized prostate cancer of whom 40 died of prostate cancer. We quantified protein expression of the markers in tumor tissue by immunohistochemistry and stratified the cohort by quintiles according to risk classification. We accounted for clinical variables (age, Gleason, nuclear grade, and tumor volume) using Cox regression and calculated receiver operator curves to compare discriminatory ability. The hazard ratio of prostate cancer death increased with increasing risk classification by the multigene model, with a 16-fold greater risk comparing highest-risk versus lowest-risk strata, and predicted outcome independent of clinical factors (P = 0.002). The best discrimination came from combining information from the multigene markers and clinical data, which perfectly classified the lowest-risk stratum where no one developed lethal disease; using the two lowest-risk groups as reference, the hazard ratio (95% confidence interval) was 11.3 (4.0-32.8) for the highest-risk group and difference in mortality at 15 years was 60% (50-70%). The combined model provided greater discriminatory ability (area under the curve = 0.78) than the clinical model alone (area under the curve = 0.71; P = 0.04). Molecular tumor markers can add to clinical variables to help distinguish lethal and indolent prostate cancer and hold promise to guide treatment decisions. 

Ämnesord

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

Nyckelord

Aged
DNA; Neoplasm/*genetics
Follow-Up Studies
Gene Expression Profiling
Gene Expression Regulation; Neoplastic
Humans
In Situ Hybridization; Fluorescence
Male
Phenotype
Prognosis
Prostatic Neoplasms/metabolism/*mortality/pathology
Retrospective Studies
Serine Endopeptidases/biosynthesis/*genetics
Severity of Illness Index
Survival Rate/trends
Sweden/epidemiology
Time Factors
MEDICINE
MEDICIN
Surgery
Kirurgi
Oncology
Onkologi
Onkologi
Oncology

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