Verification of the effectiveness of fucosylated haptoglobin as a pancreatic cancer marker in clinical diagnosis

被引:4
作者
Kuwatani, Masaki [1 ]
Kawakami, Hiroshi [2 ]
Kubota, Yoshimasa [2 ]
Kawakubo, Kazumichi [1 ]
Ito, Yoichi M. [3 ]
Togo, Shinji [4 ]
Ikeda, Takaaki [5 ]
Kusama, Ken [6 ]
Kobayashi, Yuka [6 ]
Murata, Teizo [6 ]
Sakamoto, Naoya [1 ,7 ,8 ]
机构
[1] Hokkaido Univ Hosp, Dept Gastroenterol & Hepatol, Sapporo, Hokkaido, Japan
[2] Univ Miyazaki, Fac Med, Dept Gastroenterol & Hepatol, Miyazaki, Japan
[3] Hokkaido Univ, Dept Biostat, Grad Sch Med, Sapporo, Hokkaido, Japan
[4] Ishikawacho Med Clin, Yokohama, Kanagawa, Japan
[5] Yokosuka Mutual Aid Hosp, Yokosuka, Kanagawa, Japan
[6] J Oil Mills Inc, Yokohama, Kanagawa, Japan
[7] Hokkaido Univ, Dept Gastroenterol & Hepatol, Fac Med, Sapporo, Hokkaido, Japan
[8] Hokkaido Univ, Dept Gastroenterol & Hepatol, Grad Sch Med, Sapporo, Hokkaido, Japan
关键词
CA19-9; CEA; Fucosylated haptoglobin; Pancreatic cancer; Lectin; LECTIN-ANTIBODY ELISA; DIFFERENTIAL-DIAGNOSIS; TUMOR-MARKERS; REEVALUATION; CA19-9; SERA; RISK;
D O I
10.1016/j.pan.2019.04.007
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Fucosylated haptoglobin detected by Pholiota squarrosa lectin (PhoSL) that had specificity for fucose alpha 1-6 was reported as an effective biomarker for several gastrointestinal diseases. The aim of this study was to verify Fucosylated haptoglobin detected by Pholiota squarrosa lectin (PhoSL-HP) as a pancreatic cancer (PC) marker using a new method of PhoSL-ELISA. Methods: PhoSL-HP in sera from 98 PC patients and 158 non-PC samples including 32 intraductal papillary mucinous neoplasm (IPMN) patients, 21 chronic pancreatitis (CP) patients and 105 non-pancreatic disease controls (NPDC) were measured. We compared sensitivities, specificities and areas under the curves (AUC) of PhoSL-HP, CA19-9 and CEA as single markers. We also evaluated PhoSL-HP as combination marker by comparing AUC of CA19-9 combined with PhoSL-HP or CEA. Results: The sensitivities of PhoSL-HP, CA19-9 and CEA for PC were 58%, 76% and 42%, respectively. Although the specificity of PhoSL-HP for NPDC was inferior to both of CA19-9 and CEA, that for pancreatic diseases was higher than both of CA19-9 and CEA. Combined CA19-9 with PhoSL-HP, the AUC was significantly higher at 0.880 than single use of CA19-9 at 0.825 in case of distinguishing PC from other pancreatic diseases. In contrast, the AUC of CA19-9 was not elevated significantly when combined with CEA. Conclusion: PhoSL-HP would be a useful marker for PC and have sufficient complementarity for CA19-9. (C) 2019 Published by Elsevier B.V. on behalf of IAP and EPC.
引用
收藏
页码:569 / 577
页数:9
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