CA19-9 and apolipoprotein-A2 isoforms as detection markers for pancreatic cancer: a prospective evaluation
Honda, Kazufumi; Katzke, Verena A.; Hüsing, Anika; Okaya, Shinobu; Shoji, Hirokazu; Onidani, Kaoru; Olsen, Anja; Tjønneland, Anne; Overvad, Kim; Weiderpass, Elisabete; Vineis, Paolo; Muller, David; Tsilidis, Kostas; Palli, Domenico; Pala, Valeria; Tumino, Rosario; Naccarati, Alessio; Panico, Salvatore; Aleksandrova, Krasimira; Boeing, Heiner; Bueno-de-Mesquita, H. Bas; Peeters, Petra H.; Trichopoulou, Antonia; Lagiou, Pagona; Khaw, Kay Tee; Wareham, Nick; Travis, Ruth C.; Merino, Susana; Duell, Eric J.; Rodríguez-Barranco, Miguel; Chirlaque, María Dolores; Barricarte, Aurelio; Rebours, Vinciane; Boutron-Ruault, Marie Chiristine; Romana Mancini, Francesca; Brennan, Paul; Scelo, Ghislaine; Manjer, Jonas; Sund, Malin; Öhlund, Daniel; Canzian, Federico; Kaaks, Rudolf
(2019) International Journal of Cancer, volume 144, issue 8, pp. 1877 - 1887
(Article)
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
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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.
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Keywords: apolipoprotein A2, CA19-9, early detection, isoforms, pancreatic cancer, prospective study, Pancreas/diagnostic imaging, Predictive Value of Tests, Prospective Studies, Enzyme-Linked Immunosorbent Assay, Humans, Middle Aged, CA-19-9 Antigen/blood, Male, Case-Control Studies, Early Detection of Cancer/methods, Time Factors, Pancreatic Neoplasms/blood, Protein Isoforms/analysis, Adult, Female, ROC Curve, Aged, Apolipoprotein A-II/blood, Oncology, Cancer Research, Research Support, Non-U.S. Gov't, Journal Article, Evaluation Studies
ISSN: 0020-7136
Publisher: Wiley-Liss Inc.
Note: Funding Information: Key words: pancreatic cancer, early detection, CA19-9, apolipoprotein A2, isoforms, prospective study Abbreviations: AUC: Area under the curve; EPIC: European Prospective Investigation into Cancer; EUS: Endoscopic ultrasonography; IPMN: Intraductal papillary mucinous neoplasia; NCI EDRN: US National Cancer Center Early Detection Research Network; PDAC: Pancreatic ductal adenocarcinomas; ROC: Receiver operating characteristic; UKCTOCS: UK Collaborative Trial of Ovarian Cancer Screening Additional Supporting Information may be found in the online version of this article. K.H. and V.A.K. contributed equally to this work Conflict of interest: The authors declare no conflict of interest and no specific disclosures to be made. Kazufumi Honda is coinventor of a patent, held by Tokyo National Cancer Center Research Institute and Tory company, for the use of “apolipoprotein-A2 isoforms” for early detection of pancreatic disease. Grant sponsor: Practical Research for Innovative Cancer Control; Grant numbers: 18ck0106280h0002; Grant sponsor: Project for Cancer Research and Therapeutic Evolution (P-CREATE); Grant sponsor: Japan Agency for Medical Research and Development. DOI: 10.1002/ijc.31900 History: Received 21 Feb 2018; Accepted 13 Jul 2018; Online 27 Sep 2018 Correspondence to: Rudolf Kaaks, Division of Cancer Epidemiology, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, 69120 Heidelberg, Germany, Tel.: +49 6221 422219, Fax: ++49 6221 42 2203; E-mail: r.kaaks@dkfz.de; or Kazufumi Honda; Department of Biomarker for Early Detection of Cancer, National Cancer Center Research Institute, 104-0045 Tokyo, Japan, Tel.: +81 3 3542 2511, Fax: ++81 3 3547 6045, E-mail: khonda@ncc.go.jp Publisher Copyright: © 2018 UICC
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