Genome-wide association study of prostate cancer-specific survival

Robert Szulkin; Robert Karlsson; Thomas Whitington; Markus Aly; Henrik Gronberg; 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; Timothy J Key; Ruth C Travis; David E Neal; Jenny L Donovan; Freddie C Hamdy; Paul D P Pharoah; Nora Pashayan; Kay-Tee Khaw; Janet L Stanford; Stephen N Thibodeau; Shannon K McDonnell; Daniel J Schaid; Christiane Maier; Walther Vogel; Manuel Luedeke; Kathleen Herkommer; Adam S Kibel; Cezary Cybulski; Jan Lubiński; Wojciech Kluźniak; Lisa Cannon-Albright; Hermann Brenner; Volker Herrmann; Bernd Holleczek; Jong Y Park; Thomas A Sellers; Hui-Yi Lim; Chavdar Slavov; Radka P Kaneva; Vanio I Mitev; PRACTICAL consortium

doi:10.1158/1055-9965.epi-15-0543

Genome-wide association study of prostate cancer-specific survival

Robert Szulkin, Robert Karlsson, Thomas Whitington, Markus Aly, Henrik Gronberg, 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 NordestgaardTimothy J Key, Ruth C Travis, David E Neal, Jenny L Donovan, Freddie C Hamdy, Paul D P Pharoah, Nora Pashayan, Kay-Tee Khaw, Janet L Stanford, Stephen N Thibodeau, Shannon K McDonnell, Daniel J Schaid, Christiane Maier, Walther Vogel, Manuel Luedeke, Kathleen Herkommer, Adam S Kibel, Cezary Cybulski, Jan Lubiński, Wojciech Kluźniak, Lisa Cannon-Albright, Hermann Brenner, Volker Herrmann, Bernd Holleczek, Jong Y Park, Thomas A Sellers, Hui-Yi Lim, Chavdar Slavov, Radka P Kaneva, Vanio I Mitev, PRACTICAL consortium

Department of Clinical Medicine

24 Citations (Scopus)

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
Journal	Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology
Volume	24
Issue number	11
Pages (from-to)	1796-1800
Number of pages	5
ISSN	1055-9965
DOIs	https://doi.org/10.1158/1055-9965.epi-15-0543
Publication status	Published - Nov 2015

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Szulkin, R., Karlsson, R., Whitington, T., Aly, M., Gronberg, H., Eeles, R. A., Easton, D. F., Kote-Jarai, Z., Al Olama, A. A., Benlloch, S., Muir, K., Giles, G. G., Southey, M. C., FitzGerald, L. M., Henderson, B. E., Schumacher, F. R., Haiman, C. A., Sipeky, C., Tammela, T. L. J., ... PRACTICAL consortium (2015). Genome-wide association study of prostate cancer-specific survival. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 24(11), 1796-1800. https://doi.org/10.1158/1055-9965.epi-15-0543

Genome-wide association study of prostate cancer-specific survival. / Szulkin, Robert; Karlsson, Robert; Whitington, Thomas et al.

In: Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, Vol. 24, No. 11, 11.2015, p. 1796-1800.

Research output: Contribution to journal › Journal article › Research › peer-review

Szulkin, R, Karlsson, R, Whitington, T, Aly, M, Gronberg, H, Eeles, RA, Easton, DF, Kote-Jarai, Z, Al Olama, AA, Benlloch, S, Muir, K, Giles, GG, Southey, MC, FitzGerald, LM, Henderson, BE, Schumacher, FR, Haiman, CA, Sipeky, C, Tammela, TLJ, Nordestgaard, BG, Key, TJ, Travis, RC, Neal, DE, Donovan, JL, Hamdy, FC, Pharoah, PDP, Pashayan, N, Khaw, K-T, Stanford, JL, Thibodeau, SN, McDonnell, SK, Schaid, DJ, Maier, C, Vogel, W, Luedeke, M, Herkommer, K, Kibel, AS, Cybulski, C, Lubiński, J, Kluźniak, W, Cannon-Albright, L, Brenner, H, Herrmann, V, Holleczek, B, Park, JY, Sellers, TA, Lim, H-Y, Slavov, C, Kaneva, RP, Mitev, VI & PRACTICAL consortium 2015, 'Genome-wide association study of prostate cancer-specific survival', Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, vol. 24, no. 11, pp. 1796-1800. https://doi.org/10.1158/1055-9965.epi-15-0543

Szulkin R, Karlsson R, Whitington T, Aly M, Gronberg H, Eeles RA et al. Genome-wide association study of prostate cancer-specific survival. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology. 2015 Nov;24(11):1796-1800. doi: 10.1158/1055-9965.epi-15-0543

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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.",

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AU - Szulkin, Robert

AU - Karlsson, Robert

AU - Whitington, Thomas

AU - Aly, Markus

AU - Gronberg, Henrik

AU - Eeles, Rosalind A

AU - Easton, Douglas F

AU - Kote-Jarai, Zsofia

AU - Al Olama, Ali Amin

AU - Benlloch, Sara

AU - Muir, Kenneth

AU - Giles, Graham G

AU - Southey, Melissa C

AU - FitzGerald, Liesel M

AU - Henderson, Brian E

AU - Schumacher, Fredrick R

AU - Haiman, Christopher A

AU - Sipeky, Csilla

AU - Tammela, Teuvo L J

AU - Nordestgaard, Børge G

AU - Key, Timothy J

AU - Travis, Ruth C

AU - Neal, David E

AU - Donovan, Jenny L

AU - Hamdy, Freddie C

AU - Pharoah, Paul D P

AU - Pashayan, Nora

AU - Khaw, Kay-Tee

AU - Stanford, Janet L

AU - Thibodeau, Stephen N

AU - McDonnell, Shannon K

AU - Schaid, Daniel J

AU - Maier, Christiane

AU - Vogel, Walther

AU - Luedeke, Manuel

AU - Herkommer, Kathleen

AU - Kibel, Adam S

AU - Cybulski, Cezary

AU - Lubiński, Jan

AU - Kluźniak, Wojciech

AU - Cannon-Albright, Lisa

AU - Brenner, Hermann

AU - Herrmann, Volker

AU - Holleczek, Bernd

AU - Park, Jong Y

AU - Sellers, Thomas A

AU - Lim, Hui-Yi

AU - Slavov, Chavdar

AU - Kaneva, Radka P

AU - Mitev, Vanio I

AU - PRACTICAL consortium

PY - 2015/11

Y1 - 2015/11

N2 - 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.

AB - 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.

U2 - 10.1158/1055-9965.epi-15-0543

DO - 10.1158/1055-9965.epi-15-0543

M3 - Journal article

C2 - 26307654

SN - 1055-9965

VL - 24

SP - 1796

EP - 1800

JO - Cancer Epidemiology, Biomarkers & Prevention

JF - Cancer Epidemiology, Biomarkers & Prevention

IS - 11

ER -

Genome-wide association study of prostate cancer-specific survival

Abstract

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