前列腺癌
癌症
前列腺
肿瘤科
全基因组关联研究
医学
生物
内科学
遗传学
单核苷酸多态性
基因
基因型
作者
Robert Szulkin,Robert Karlsson,Thomas Whitington,Markus Aly,Henrik Grönberg,Rosalind A. Eeles,Douglas F. Easton,Zsofia Kote‐Jarai,Ali Amin Al Olama,Sara Benlloch,Kenneth Muir,Graham G. Giles,Melissa C. Southey,Liesel M. FitzGerald,Brian E. Henderson,Fredrick R. Schumacher,Christopher A. Haiman,Csilla Sipeky,Teuvo L.J. Tammela,Børge G. Nordestgaard
标识
DOI:10.1158/1055-9965.epi-15-0543
摘要
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI