Ki-67 predicts disease recurrence and poor prognosis in pancreatic neuroendocrine neoplasms

被引:74
作者
Hamilton, Nicholas A. [1 ]
Liu, Ta-Chiang [2 ]
Cavatiao, Antonino [1 ]
Mawad, Kareem [1 ]
Chen, Ling [3 ]
Strasberg, Steven S. [1 ]
Linehan, David C. [1 ]
Cao, Dengfeng [2 ]
Hawkins, William G. [1 ]
机构
[1] Washington Univ, Dept Surg, St Louis, MO 63130 USA
[2] Washington Univ, Dept Pathol & Immunol, St Louis, MO USA
[3] Siteman Canc Ctr, Biostat Core, St Louis, MO USA
关键词
TUMORS; SYSTEM;
D O I
10.1016/j.surg.2012.02.011
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background. Pancreatic neuroendocrine neoplasms are rare malignancies for which the ideal staging method remains controversial. Ki-67 is a cell proliferation marker that has been shown to have some utility in predicting prognosis in neuroendocrine neoplasms. We sought to test the predictive ability of Ki-67 staining for disease recurrence and overall survival (OS) in pancreatic neuroendocrine neoplasms. Methods. The medical records of patients who underwent pancreatic resection for pancreatic neuroendocrine neoplasms at a tertiary referral hospital from 1994 to 2009 were reviewed. The pathologic specimens of all were stained for Ki-67 and recorded as percentage of cells staining positive per high-powered field. The 10-year disease-free and OSs were analyzed. Results. We identified 140 patients. Gender and age were not associated with increased risk of disease recurrence. Patients with tumors >4 cm or with Ki-67 staining >9% were more likely to have disease recurrence (P = .0454 and .047) and have decreased OS (P < .0001 and .0007). Conclusion. Increasing tumor size and increasing Ki-67 staining both correlate with increased risk of disease recurrence and decreased OS. Designing a staging system that incorporates both of these clinical variables will enable better identification of patients at risk for recurrent pancreatic neuroendocrine neoplasms. (Surgery) 2012;152:107-13.)
引用
收藏
页码:107 / 113
页数:7
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