A Routine Laboratory Data-Based Model for Predicting Recurrence After Curative Resection of Stage II Colorectal Cancer

被引:3
|
作者
Ye, Zhong [1 ]
Wang, Chun [1 ,2 ]
Guo, Limin [3 ]
Palazzo, Juan P. [4 ]
Han, Zhixing [5 ]
Lai, Yinzhi [1 ]
Jiang, Jing [1 ]
Posey, James A. [1 ]
Mallick, Atrayee Basu [1 ]
Li, Bingshan [6 ]
Jiang, Li [3 ]
Yang, Hushan [1 ]
机构
[1] Thomas Jefferson Univ, Dept Med Oncol, Sidney Kimmel Canc Ctr, Philadelphia, PA 19107 USA
[2] Nantong Univ, Dept Environm Hlth, Sch Publ Hlth, Nantong, Peoples R China
[3] Capital Med Univ, Beijing Ditan Hosp, Dept Hepatobiliary Surg, Beijing 100015, Peoples R China
[4] Thomas Jefferson Univ, Dept Pathol, Philadelphia, PA 19107 USA
[5] Capital Med Univ, Beijing Ditan Hosp, Dept Urol, Beijing, Peoples R China
[6] Vanderbilt Univ, Dept Mol Physiol & Biophys, Nashville, TN 37232 USA
关键词
COLON-CANCER; CARCINOEMBRYONIC ANTIGEN; ADJUVANT CHEMOTHERAPY; SURVIVAL; SURVEILLANCE; HEMOGLOBIN; BIOMARKERS; LUNG; IDENTIFICATION; PROGNOSIS;
D O I
10.6004/jnccn.2018.7048
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Use of chemotherapy in stage II colorectal cancer (CRC) is controversial because it improves survival only in some patients. We aimed to develop a statistical model using routine and readily available blood tests to predict the prognosis of patients with stage II CRC and to identify which patients are likely to benefit from chemotherapy. Methods: We divided 422 patients with stage II CRC into a training and a testing set. The association of routine laboratory variables and disease-free survival (DFS) was analyzed. A prognostic model was developed incorporating clinically relevant laboratory variables with demographic and tumor characteristics. A prognostic score was derived by calculating the sum of each variable weighted by its regression coefficient in the model. Model performance was evaluated by constructing receiver operating characteristic curves and calculating the area under the curve (AUC). Results: Significant associations were seen between 5 laboratory variables and patient DFS in univariate analyses. After stepwise selection, 3 variables (carcinoembryonic antigen, hemoglobin, creatinine) were retained in the multivariate model with an AUC of 0.75. Compared with patients with a low prognostic score, those with a medium and high prognostic score had a 1.99- and 4.78-fold increased risk of recurrence, respectively. The results from the training set were validated in the testing set. Moreover, chemotherapy significantly improved DFS in high-risk patients, but not in lowand medium-risk patients. Conclusions: A routine laboratory variable-based model may help predict DFS of patients with stage II CRC and identify high-risk patients more likely to benefit from chemotherapy.
引用
收藏
页码:1183 / 1192
页数:10
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