Development and validation of a prognostic nomogram for gastrointestinal stromal tumors in the postimatinib era: A study based on the SEER database and a Chinese cohort

被引:1
|
作者
Wang, Shu [1 ]
Wang, Yuhao [1 ]
Luo, Jialin [1 ]
Wang, Haoyuan [1 ]
Zhao, Yan [1 ]
Nie, Yongzhan [2 ,3 ,4 ]
Yang, Jianjun [1 ]
机构
[1] Fourth Mil Med Univ, Xi Jing Hosp, Dept Digest Surg, 127 Changle West Rd, Xian 710032, Peoples R China
[2] Fourth Mil Med Univ, Ctr Digest Dis, Natl Clin Res Ctr Digest Dis, State Key Lab Canc Biol, Xian, Peoples R China
[3] Fourth Mil Med Univ, Xijing Hosp Digest Dis, Xian, Peoples R China
[4] Fourth Mil Med Univ, Xijing Hosp, Natl Clin Res Ctr Digest Dis & Digest Dis, State Key Lab Canc Biol, Xian 710032, Peoples R China
来源
CANCER MEDICINE | 2023年 / 12卷 / 15期
基金
中国国家自然科学基金;
关键词
gastrointestinal stromal tumor; nomogram; prognostic factors; SEER analyses; PHASE-II TRIAL; IMATINIB MESYLATE; SARCOMA GROUP; RISK STRATIFICATION; PDGFRA MUTATIONS; RANDOMIZED-TRIAL; DOSE IMATINIB; POPULATION; SURVIVAL; EFFICACY;
D O I
10.1002/cam4.6240
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: After the standardization, recording and follow -up of imatinib use that significantly prolongs survival of gastrointestinal stromal tumors (GISTs), a comprehensive reassessment of the prognosis of GISTs is necessary and more conductive to treatment options.Methods: A total of 2185 GISTs between 2013 and 2016 were obtained from the Surveillance, Epidemiology, and End Results database and comprised our training (n = 1456) and internal validation cohorts (n = 729). The risk factors extracted from univariate and multivariate analyses were used to establish a predictive nomogram. The model was evaluated and tested in the validation cohort internally and in 159 patients with GIST diagnosed between January 2015 and June 2017 in Xijing Hospital externally.Results: The median OS was 49 months (range, 0- 83 months) in the training cohort and 51 months (0- 83 months) in the validation cohort. The concordance index (C-index) of the nomogram was 0.777 (95% CI, 0.752- 0.802) and 0.7787 (0.7785, bootstrap corrected) in training and internal validation cohorts, respectively, and 0.7613 (0.7579, bootstrap corrected) in the external validation cohort. Receiver operating characteristic curves and calibration curves for 1-, 3-, and 5 -year overall survival (OS) showed a high degree of discrimination and calibration. The area under the curve showed that the new model performed better than the TNM staging system. In addition, the model could be dynamically visualized on a webpage.Conclusion: We developed a comprehensive survival prediction model for assessing the 1-, 3-and 5 -year OS of patients with GIST in the postimatinib era. This predictive model outperforms the traditional TNM staging system and sheds light on the improvement of the prognostic prediction and the selection of treatment strategies for GISTs.
引用
收藏
页码:15970 / 15982
页数:13
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