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CA125 is Superior to CA19-9 in Predicting the Resectability of Pancreatic Cancer

  • Original Article
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Journal of Gastrointestinal Surgery Aims and scope

Abstract

Background

Although carbohydrate antigen 19-9 (CA19-9) has been reported as a biomarker to predict the resectability of pancreatic cancer, several limitations have restricted its clinical use.

Methods

The potential of several serum tumor markers (CA19-9, CA125, CA50, CA242, CA724, carcinoembryonic antigen (CEA), and alpha-fetoprotein (AFP)) to predict the resectability of pancreatic cancer was evaluated by receiver operating characteristic (ROC) analysis in a series of 212 patients with proven pancreatic cancer.

Results

Compared with other tumor markers including CA19-9, CA125 has a superior predictive value (CA19-9, ROC area 0.66, cutoff value 289.40 U/mL; CA125, ROC area 0.81, cutoff value 19.70 U/mL). In addition, for patients with unresectable diseases misjudged by CT as resectable, the percentage of CA125 over selected cutoff value was higher than that of CA19-9 (CA19-9, 70.27 %; CA125, 81.08 %).

Conclusion

CA125 is superior to CA19-9 in predicting the resectability of pancreatic cancer. Aberrant high levels of CA125 may indicate unresectable pancreatic cancer.

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Acknowledgments

We thank Dr. Jingjing Feng and Dr. Kefu Liu for their expert technical assistance. This study was supported in part by the Sino-German Center (GZ857), by the Science Foundation of Shanghai (13ZR1407500), and by the National Science Foundation of China (grant nos. 81101807, 81001058, 81372649, 81372653, and 81172276).

Conflict of Interest

The authors indicated no potential conflicts of interest.

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Correspondence to Xianjun Yu.

Additional information

Guopei Luo, Zhiwen Xiao, and Jiang Long have equal contribution.

The paper is not based on a previous communication to a society or meeting.

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Luo, G., Xiao, Z., Long, J. et al. CA125 is Superior to CA19-9 in Predicting the Resectability of Pancreatic Cancer. J Gastrointest Surg 17, 2092–2098 (2013). https://doi.org/10.1007/s11605-013-2389-9

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  • DOI: https://doi.org/10.1007/s11605-013-2389-9

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