| Literature DB >> 30259989 |
Kazufumi Honda1,2, Verena A Katzke3, Anika Hüsing3, Shinobu Okaya1, Hirokazu Shoji1,4, Kaoru Onidani1, Anja Olsen5, Anne Tjønneland5, Kim Overvad6, Elisabete Weiderpass7,8,9,10, Paolo Vineis11, David Muller11, Kostas Tsilidis11,12, Domenico Palli13, Valeria Pala14, Rosario Tumino15, Alessio Naccarati16, Salvatore Panico17, Krasimira Aleksandrova18, Heiner Boeing18, H Bas Bueno-de-Mesquita19,20,11,21, Petra H Peeters22,23, Antonia Trichopoulou24, Pagona Lagiou25, Kay-Tee Khaw26, Nick Wareham27, Ruth C Travis28, Susana Merino29, Eric J Duell30, Miguel Rodríguez-Barranco31,32, María Dolores Chirlaque33, Aurelio Barricarte32,34,35, Vinciane Rebours36,37, Marie-Chiristine Boutron-Ruault38,39, Francesca Romana Mancini37,38, Paul Brennan40, Ghislaine Scelo40, Jonas Manjer41, Malin Sund42, Daniel Öhlund43, Federico Canzian44, Rudolf Kaaks3.
Abstract
Recently, we identified unique processing patterns of apolipoprotein A2 (ApoA2) in patients with pancreatic cancer. Our study provides a first prospective evaluation of an ApoA2 isoform ("ApoA2-ATQ/AT"), alone and in combination with carbohydrate antigen 19-9 (CA19-9), as an early detection biomarker for pancreatic cancer. We performed ELISA measurements of CA19-9 and ApoA2-ATQ/AT in 156 patients with pancreatic cancer and 217 matched controls within the European EPIC cohort, using plasma samples collected up to 60 months prior to diagnosis. The detection discrimination statistics were calculated for risk scores by strata of lag-time. For CA19-9, in univariate marker analyses, C-statistics to distinguish future pancreatic cancer patients from cancer-free individuals were 0.80 for plasma taken ≤6 months before diagnosis, and 0.71 for >6-18 months; for ApoA2-ATQ/AT, C-statistics were 0.62, and 0.65, respectively. Joint models based on ApoA2-ATQ/AT plus CA19-9 significantly improved discrimination within >6-18 months (C = 0.74 vs. 0.71 for CA19-9 alone, p = 0.022) and ≤ 18 months (C = 0.75 vs. 0.74, p = 0.022). At 98% specificity, and for lag times of ≤6, >6-18 or ≤ 18 months, sensitivities were 57%, 36% and 43% for CA19-9 combined with ApoA2-ATQ/AT, respectively, vs. 50%, 29% and 36% for CA19-9 alone. Compared to CA19-9 alone, the combination of CA19-9 and ApoA2-ATQ/AT may improve detection of pancreatic cancer up to 18 months prior to diagnosis under usual care, and may provide a useful first measure for pancreatic cancer detection prior to imaging.Entities:
Keywords: CA19-9; apolipoprotein A2; early detection; isoforms; pancreatic cancer; prospective study
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Year: 2018 PMID: 30259989 PMCID: PMC6760974 DOI: 10.1002/ijc.31900
Source DB: PubMed Journal: Int J Cancer ISSN: 0020-7136 Impact factor: 7.396