A prospective evaluation of early detection biomarkers for ovarian cancer in the European EPIC cohort.

<h4>Purpose</h4> <p>About 60% of ovarian cancers are diagnosed at late stage, when5-year survival is less than 30% in contrast to 90% for local disease. This has prompted search for early detection biomarkers. For initial testing, specimens taken months or years before ovarian canc...

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Main Authors: Terry, K, Schock, H, Fortner, R, Hüsing, A, Fichorova, R, Yamamoto, H, Vitonis, A, Johnson, T, Overvad, K, Tjønneland, A, Boutron-Ruault, M, Mesrine, S, Severi, G, Dossus, L, Rinaldi, S, Boeing, H, Benetou, V, Lagiou, P, Trichopoulou, A, Krogh, V, Kuhn, E, Panico, S, Bueno-de-Mesquita, H, Onland-Moret, N, Peeters, P, Gram, I, Weiderpass, E, Duell, E, Sanchez, M, Ardanaz, E, Etxezarreta, N, Navarro, C, Idahl, A, Lundin, E, Jirström, K, Manjer, J, Wareham, N, Khaw, K, Smith Byrne, K, Travis, R, Gunter, M, Merritt, M, Riboli, E, Cramer, D, Kaaks, R
Format: Journal article
Language:English
Published: American Association for Cancer Research 2016
_version_ 1826257070077247488
author Terry, K
Schock, H
Fortner, R
Hüsing, A
Fichorova, R
Yamamoto, H
Vitonis, A
Johnson, T
Overvad, K
Tjønneland, A
Boutron-Ruault, M
Mesrine, S
Severi, G
Dossus, L
Rinaldi, S
Boeing, H
Benetou, V
Lagiou, P
Trichopoulou, A
Krogh, V
Kuhn, E
Panico, S
Bueno-de-Mesquita, H
Onland-Moret, N
Peeters, P
Gram, I
Weiderpass, E
Duell, E
Sanchez, M
Ardanaz, E
Etxezarreta, N
Navarro, C
Idahl, A
Lundin, E
Jirström, K
Manjer, J
Wareham, N
Khaw, K
Smith Byrne, K
Travis, R
Gunter, M
Merritt, M
Riboli, E
Cramer, D
Kaaks, R
author_facet Terry, K
Schock, H
Fortner, R
Hüsing, A
Fichorova, R
Yamamoto, H
Vitonis, A
Johnson, T
Overvad, K
Tjønneland, A
Boutron-Ruault, M
Mesrine, S
Severi, G
Dossus, L
Rinaldi, S
Boeing, H
Benetou, V
Lagiou, P
Trichopoulou, A
Krogh, V
Kuhn, E
Panico, S
Bueno-de-Mesquita, H
Onland-Moret, N
Peeters, P
Gram, I
Weiderpass, E
Duell, E
Sanchez, M
Ardanaz, E
Etxezarreta, N
Navarro, C
Idahl, A
Lundin, E
Jirström, K
Manjer, J
Wareham, N
Khaw, K
Smith Byrne, K
Travis, R
Gunter, M
Merritt, M
Riboli, E
Cramer, D
Kaaks, R
author_sort Terry, K
collection OXFORD
description <h4>Purpose</h4> <p>About 60% of ovarian cancers are diagnosed at late stage, when5-year survival is less than 30% in contrast to 90% for local disease. This has prompted search for early detection biomarkers. For initial testing, specimens taken months or years before ovarian cancer diagnosis are the best source of information to evaluate early detection biomarkers. Here we evaluate the most promising ovarian cancer screening biomarkers in prospectively collected samples from the European Prospective Investigation into Cancerand Nutrition study.</p> <h4>Experimental Design</h4> <p>We measured CA125, HE4, CA72.4 and CA15.3 in 810 invasive epithelial ovarian cancer cases and 1,939 controls. We calculated the sensitivity at 95% and 98% specificity as well as Area under the Receiver Operator Curve (C-statistic) for each marker individually and in combination. Additionally, we evaluated marker performance by stage at diagnosis and time between blood draw and diagnosis. </p> <h4>Results</h4> <p>We observed the best discrimination between cases and controlswithin six months of diagnosis for CA125 (C-statistic=0.92), then HE4 (0.84), CA72.4 (0.77), and CA15.3 (0.73). Marker performance declined with longer time between blood draw and diagnosis and for earlier staged disease. However, assessment of discriminatory ability at early stage was limited by small numbers. Combinations of markers performed modestly, but significantly better than any single marker. </p> <h4>Conclusions</h4> <p>CA125 remains the single best marker for the early detection of invasive epithelial ovarian cancer, but can be slightly improved by combining with other markers. Identifying novel markers for ovarian cancer will require studies including larger numbers of early stage cases. </p>
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spelling oxford-uuid:03700a7e-3e18-4811-8299-a3ba3fb88ec02022-03-26T08:46:16ZA prospective evaluation of early detection biomarkers for ovarian cancer in the European EPIC cohort.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:03700a7e-3e18-4811-8299-a3ba3fb88ec0EnglishSymplectic Elements at OxfordAmerican Association for Cancer Research2016Terry, KSchock, HFortner, RHüsing, AFichorova, RYamamoto, HVitonis, AJohnson, TOvervad, KTjønneland, ABoutron-Ruault, MMesrine, SSeveri, GDossus, LRinaldi, SBoeing, HBenetou, VLagiou, PTrichopoulou, AKrogh, VKuhn, EPanico, SBueno-de-Mesquita, HOnland-Moret, NPeeters, PGram, IWeiderpass, EDuell, ESanchez, MArdanaz, EEtxezarreta, NNavarro, CIdahl, ALundin, EJirström, KManjer, JWareham, NKhaw, KSmith Byrne, KTravis, RGunter, MMerritt, MRiboli, ECramer, DKaaks, R<h4>Purpose</h4> <p>About 60% of ovarian cancers are diagnosed at late stage, when5-year survival is less than 30% in contrast to 90% for local disease. This has prompted search for early detection biomarkers. For initial testing, specimens taken months or years before ovarian cancer diagnosis are the best source of information to evaluate early detection biomarkers. Here we evaluate the most promising ovarian cancer screening biomarkers in prospectively collected samples from the European Prospective Investigation into Cancerand Nutrition study.</p> <h4>Experimental Design</h4> <p>We measured CA125, HE4, CA72.4 and CA15.3 in 810 invasive epithelial ovarian cancer cases and 1,939 controls. We calculated the sensitivity at 95% and 98% specificity as well as Area under the Receiver Operator Curve (C-statistic) for each marker individually and in combination. Additionally, we evaluated marker performance by stage at diagnosis and time between blood draw and diagnosis. </p> <h4>Results</h4> <p>We observed the best discrimination between cases and controlswithin six months of diagnosis for CA125 (C-statistic=0.92), then HE4 (0.84), CA72.4 (0.77), and CA15.3 (0.73). Marker performance declined with longer time between blood draw and diagnosis and for earlier staged disease. However, assessment of discriminatory ability at early stage was limited by small numbers. Combinations of markers performed modestly, but significantly better than any single marker. </p> <h4>Conclusions</h4> <p>CA125 remains the single best marker for the early detection of invasive epithelial ovarian cancer, but can be slightly improved by combining with other markers. Identifying novel markers for ovarian cancer will require studies including larger numbers of early stage cases. </p>
spellingShingle Terry, K
Schock, H
Fortner, R
Hüsing, A
Fichorova, R
Yamamoto, H
Vitonis, A
Johnson, T
Overvad, K
Tjønneland, A
Boutron-Ruault, M
Mesrine, S
Severi, G
Dossus, L
Rinaldi, S
Boeing, H
Benetou, V
Lagiou, P
Trichopoulou, A
Krogh, V
Kuhn, E
Panico, S
Bueno-de-Mesquita, H
Onland-Moret, N
Peeters, P
Gram, I
Weiderpass, E
Duell, E
Sanchez, M
Ardanaz, E
Etxezarreta, N
Navarro, C
Idahl, A
Lundin, E
Jirström, K
Manjer, J
Wareham, N
Khaw, K
Smith Byrne, K
Travis, R
Gunter, M
Merritt, M
Riboli, E
Cramer, D
Kaaks, R
A prospective evaluation of early detection biomarkers for ovarian cancer in the European EPIC cohort.
title A prospective evaluation of early detection biomarkers for ovarian cancer in the European EPIC cohort.
title_full A prospective evaluation of early detection biomarkers for ovarian cancer in the European EPIC cohort.
title_fullStr A prospective evaluation of early detection biomarkers for ovarian cancer in the European EPIC cohort.
title_full_unstemmed A prospective evaluation of early detection biomarkers for ovarian cancer in the European EPIC cohort.
title_short A prospective evaluation of early detection biomarkers for ovarian cancer in the European EPIC cohort.
title_sort prospective evaluation of early detection biomarkers for ovarian cancer in the european epic cohort
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