Nomogram predicting the risk of recurrence after curative‐intent resection of primary non‐metastatic gastrointestinal neuroendocrine tumors: An analysis of the U.S. Neuroendocrine Tumor Study Group

Background The risk of recurrence after resection of non‐metastatic gastro‐entero‐pancreatic neuroendocrine tumors (GEP‐NET) is poorly defined. We developed/validated a nomogram to predict risk of recurrence after curative‐intent resection. Methods A training set to develop the nomogram and test set...

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Veröffentlicht in:Journal of surgical oncology 2018-04, Vol.117 (5), p.868-878
Hauptverfasser: Merath, Katiuscha, Bagante, Fabio, Beal, Eliza W., Lopez‐Aguiar, Alexandra G., Poultsides, George, Makris, Eleftherios, Rocha, Flavio, Kanji, Zaheer, Weber, Sharon, Fisher, Alexander, Fields, Ryan, Krasnick, Bradley A., Idrees, Kamran, Smith, Paula M., Cho, Cliff, Beems, Megan, Schmidt, Carl R., Dillhoff, Mary, Maithel, Shishir K, Pawlik, Timothy M.
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Sprache:eng
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Zusammenfassung:Background The risk of recurrence after resection of non‐metastatic gastro‐entero‐pancreatic neuroendocrine tumors (GEP‐NET) is poorly defined. We developed/validated a nomogram to predict risk of recurrence after curative‐intent resection. Methods A training set to develop the nomogram and test set for validation were identified. The predictive ability of the nomogram was assessed using c‐indices. Results Among 1477 patients, 673 (46%) were included in the training set and 804 (54%) in y the test set. On multivariable analysis, Ki‐67, tumor size, nodal status, and invasion of adjacent organs were independent predictors of DFS. The risk of death increased by 8% for each percentage increase in the Ki‐67 index (HR 1.08, 95% CI, 1.05‐1.10; P 3 positive nodes had a HR of 1.81 (95% CI, 1.12‐2.87; P = 0.014) and 2.51 (95% CI, 1.50‐4.24; P 
ISSN:0022-4790
1096-9098
DOI:10.1002/jso.24985