Analysis of 6,747 Pancreatic Neuroendocrine Tumors for a Proposed Staging System

被引:37
|
作者
Martin, Robert C. G. [1 ,6 ]
Kooby, David A. [5 ]
Weber, Sharon M. [4 ]
Merchant, Nipun B. [3 ]
Parikh, Alex A. [3 ]
Cho, Clifford S. [4 ]
Ahmad, Syed A. [2 ]
Kim, Hong Jin [8 ]
Hawkins, William [7 ]
Scoggins, Charles R. [6 ]
机构
[1] Univ Louisville, Sch Med, Dept Surg, Louisville, KY 40292 USA
[2] Univ Cincinnati, Med Ctr, Dept Surg, Cincinnati, OH 45267 USA
[3] Vanderbilt Univ, Dept Surg, Med Ctr, Nashville, TN 37240 USA
[4] Univ Wisconsin Hosp, Dept Surg, Madison, WI 53792 USA
[5] Emory Univ Hosp, Dept Surg, Atlanta, GA 30322 USA
[6] Univ Louisville Hosp, Dept Surg, Louisville, KY USA
[7] Washington Univ, Med Ctr, Dept Surg, St Louis, MO USA
[8] Univ N Carolina Hosp, Dept Surg, Chapel Hill, NC USA
关键词
Pancreatic; Neuroendocrine; Staging; ADJUVANT CHEMORADIATION THERAPY; CARCINOID-TUMORS; PREDICTIVE ACCURACY; SURVIVAL-DATA; CLASSIFICATION; ADENOCARCINOMA; BENEFITS;
D O I
10.1007/s11605-010-1380-y
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Currently, no reasonable staging system exists for pancreatic neuroendocrine tumors (PNET) to guide treating physicians. The aim of this study was to devise a staging system of relevant prognostic factors to better predict overall survival in PNET. A prospective 300 patient cohort and a review of the Surveillance Epidemiology and End Results database identified 6,447 patients with PNET from 1973 to 2008. Significant prognostic factors were created for an initial. Tumor: T (T1: a parts per thousand currency sign3 cm and localized to pancreas, T2: > 3 cm and localized to the pancreas; T3: extension to adjacent organs and vessels), grade: G (G1: well/moderate and G2: poor/undifferentiated), and metastasis: M (M0: no distant mets, M1: distant mets) staging system. Significant predictors of survival on multivariate analysis included age, size, grade, and metastasis. Based on the TGM staging system: stage 1 (T1-2, G1, M0), stage 2 (T1-2, G2, M0), stage 3 (T3G2M0, Tany, G1, M1), stage 4: (Tany, G2, M1) was created with survival being statistically different between stages (p < 0.0001). Median survival rates were stage 1, 55 months; stage 2, 50 months; stage 3, 46 months; and stage 4, 25 months. Incorporation of this newly developed staging system into clinical practice will improve the ability to predict prognosis and aid in stratification of patients for clinical trials.
引用
收藏
页码:175 / 183
页数:9
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