Development and validation of a nomogram to individually predict survival of young patients with nonmetastatic gastric cancer: A retrospective cohort study

被引:14
|
作者
Wu, Chaorui [1 ,2 ]
Wang, Nianchang [1 ,2 ]
Zhou, Hong [1 ,2 ]
Wang, Tongbo [1 ,2 ]
Zhao, Dongbing [1 ,2 ]
机构
[1] Chinese Acad Med Sci, Dept Pancreat & Gastr Surg, Natl Canc Ctr, Natl Clin Res Ctr Canc,Canc Hosp, Beijing, Peoples R China
[2] Peking Union Med Coll, 17 Pan Jia Yuan South Lane, Beijing 100021, Peoples R China
来源
SAUDI JOURNAL OF GASTROENTEROLOGY | 2019年 / 25卷 / 04期
关键词
Gastric cancer; nomogram; risk factors; young patients; R0; RESECTION; CLINICOPATHOLOGICAL CHARACTERISTICS; UNITED-STATES; ADENOCARCINOMA; PROGNOSIS; OUTCOMES; DISEASE; REFLUX; ADULTS;
D O I
10.4103/sjg.SJG_378_18
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: Evidence regarding gastric cancer (GC) patients <40 years old is limited. The aim of the study was to identify risk factors affecting overall survival (OS) of young patients with nonmetastatic GC and to establish a nomogram for prognostic prediction using data from the Surveillance, Epidemiology and End Results (SEER) database. Furthermore, this study sought to externally validate this nomogram in an independent patient cohort. Patients and Methods: In this retrospective cohort study, the records of patients aged <40 years with nonmetastatic GC (n = 559), from the SEER database, between 2006 and 2015, were examined. The nomogram was established based on the Cox proportional hazards regression model using the SEER dataset. Patients with nonmetastatic GC (n = 201) in our department between 2009 and 2015 were selected as an external validation set. Discrimination and calibration were performed in both cohorts. Results: The multivariate Cox model identified race, tumor subsites, tumor size, depth of invasion, lymph node metastasis, number of examined lymph nodes, and surgery as independent covariates associated with OS. The nomogram exhibited superior discriminative power than the eighth tumor, node, metastasis (TNM) staging system in both the training set [Harrell's concordance index (C index): 0.762 vs. 0.635, P < 0.001] and validation set (C index: 0.805 vs. 0.712, P = 0.176). Calibration of the nomogram was good in both cohorts. Conclusions: We developed a nomogram predicting 3- and 5-year OS rates in young patients with nonmetastatic GC. Both the training set and validation set showed good discrimination and calibration, suggesting good clinical applicability.
引用
收藏
页码:236 / 244
页数:9
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