Assessment of the American Joint Commission on Cancer 8th Edition Staging System for Patients with Pancreatic Neuroendocrine Tumors: A Surveillance, Epidemiology, and End Results analysis
- PMID: 29380547
- PMCID: PMC5852336
- DOI: 10.1002/cam4.1336
Assessment of the American Joint Commission on Cancer 8th Edition Staging System for Patients with Pancreatic Neuroendocrine Tumors: A Surveillance, Epidemiology, and End Results analysis
Abstract
Although several staging systems have been proposed for pancreatic neuroendocrine tumors (pNETs), the optimal staging system remains unclear. Here, we aimed to assess the application of the newly revised 8th edition American Joint Committee on Cancer (AJCC) staging system for exocrine pancreatic carcinoma (EPC) to pNETs, in comparison with that of other staging systems. We identified pNETs patients from the Surveillance, Epidemiology, and End Results (SEER) database (2004-2014). Overall survival was analyzed using Kaplan-Meier curves with the log-rank test. The predictive accuracy of each staging system was assessed by the concordance index (c-index). Cox proportional hazards regression was conducted to calculate the impact of different stages. In total, 2424 patients with pNETs, including 2350 who underwent resection, were identified using SEER data. Patients with different stages were evenly stratified based on the 8th edition AJCC staging system for EPC. Kaplan-Meier curves were well separated in all patients and patients with resection using the 8th edition AJCC staging system for EPC. Moreover, the hazard ratio increased with worsening disease stage. The c-index of the 8th edition AJCC staging system for EPC was similar to that of the other systems. For pNETs patients, the 8th edition AJCC staging system for EPC exhibits good prognostic discrimination among different stages in both all patients and those with resection.
Keywords: AJCC; ENETS; pancreatic neuroendocrine tumors; prognosis; staging system.
© 2018 The Authors. Cancer Medicine published by John Wiley & Sons Ltd.
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References
-
- Hill, J. S. , McPhee J. T., McDade T. P., Zhou Z., Sullivan M. E., Whalen G. F., et al. 2009. Pancreatic neuroendocrine tumors: the impact of surgical resection on survival. Cancer 115:741–751. - PubMed
-
- Yao, J. C. , Hassan M., Phan A., Dagohoy C., Leary C., Mares J. E., et al. 2008. One hundred years after “carcinoid”: epidemiology of and prognostic factors for neuroendocrine tumors in 35,825 cases in the United States. J. Clin. Oncol. 26:3063–3072. - PubMed
-
- Fitzgerald, T. L. , Hickner Z. J., Schmitz M., and Kort E. J.. 2008. Changing incidence of pancreatic neoplasms: a 16‐year review of statewide tumor registry. Pancreas 37:134–138. - PubMed
-
- Keutgen, X. M. , Nilubol N., and Kebebew E.. 2016. Malignant‐functioning neuroendocrine tumors of the pancreas: a survival analysis. Surgery 159:1382–1389. - PubMed
-
- Krampitz, G. W. , and Norton J. A.. 2013. Pancreatic neuroendocrine tumors. Curr. Probl. Surg. 50:509–545. - PubMed
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