Abstract
Background: Unnecessary intervention and overtreatment of indolent disease are common challenges in clinical management of prostate cancer. Improved tools to distinguish lethal from indolent disease are critical. Methods: We performed a genome-wide survival analysis of cause-specific death in 24,023 prostate cancer patients (3,513 disease-specific deaths) from the PRACTICAL and BPC3 consortia. Top findings were assessed for replication in a Norwegian cohort (CONOR). Results: We observed no significant association between genetic variants and prostate cancer survival. Conclusions: Common genetic variants with large impact on prostate cancer survival were not observed in this study. Impact: Future studies should be designed for identification of rare variants with large effect sizes or common variants with small effect sizes.
Original language | English |
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Pages (from-to) | 1796-1800 |
Number of pages | 5 |
Journal | Cancer Epidemiology, Biomarkers & Prevention |
Volume | 24 |
Issue number | 11 |
DOIs | |
Publication status | Published - 2015 |
Publication type | A1 Journal article-refereed |
Publication forum classification
- Publication forum level 2