Postoperative Nomogram for Predicting Cancer-Specific Mortality in Medullary Thyroid Cancer

被引:43
|
作者
Ho, Allen S. [1 ]
Wang, Lu [2 ]
Palmer, Frank L. [3 ]
Yu, Changhong [2 ]
Toset, Arnbjorn [3 ]
Patel, Snehal [3 ]
Kattan, Michael W. [2 ]
Tuttle, R. Michael [4 ]
Ganly, Ian [3 ]
机构
[1] Cedars Sinai Med Ctr, Dept Surg, Los Angeles, CA 90048 USA
[2] Cleveland Clin, Dept Quantitat Hlth Sci, Cleveland, OH 44106 USA
[3] Mem Sloan Kettering Canc Ctr, Dept Surg, Head & Neck Serv, New York, NY 10021 USA
[4] Mem Sloan Kettering Canc Ctr, Dept Med, Serv Endocrinol, New York, NY 10021 USA
关键词
ANTIGEN DOUBLING-TIMES; PROGNOSTIC-FACTORS; PROSTATE-CANCER; MULTIVARIATE-ANALYSIS; BIOCHEMICAL CURE; SERUM CALCITONIN; BREAST-CANCER; FOLLOW-UP; CARCINOMA; RECURRENCE;
D O I
10.1245/s10434-014-4208-2
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Medullary thyroid cancer (MTC) is a rare thyroid cancer accounting for 5 % of all thyroid malignancies. The purpose of our study was to design a predictive nomogram for cancer-specific mortality (CSM) utilizing clinical, pathological, and biochemical variables in patients with MTC. MTC patients managed entirely at Memorial Sloan-Kettering Cancer Center between 1986 and 2010 were identified. Patient, tumor, and treatment characteristics were recorded, and variables predictive of CSM were identified by univariable analyses. A multivariable competing risk model was then built to predict the 10-year cancer specific mortality of MTC. All predictors of interest were added in the starting full model before selection, including age, gender, pre- and postoperative serum calcitonin, pre- and postoperative CEA, RET mutation status, perivascular invasion, margin status, pathologic T status, pathologic N status, and M status. Stepdown method was used in model selection to choose predictive variables. Of 249 MTC patients, 22.5 % (56/249) died from MTC, whereas 6.4 % (16/249) died secondary to other causes. Mean follow-up period was 87 +/- A 67 months. The seven variables with the highest predictive accuracy for cancer specific mortality included age, gender, postoperative calcitonin, perivascular invasion, pathologic T status, pathologic N status, and M status. These variables were used to create the final nomogram. Discrimination from the final nomogram was measured at 0.77 with appropriate calibration. We describe the first nomogram that estimates cause-specific mortality in individual patients with MTC. This predictive nomogram will facilitate patient counseling in terms of prognosis and subsequent clinical follow up.
引用
收藏
页码:2700 / 2706
页数:7
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