Relationship Between Tumor Size and Survival in Non-Small-Cell Lung Cancer (NSCLC) An Analysis of the Surveillance, Epidemiology, and End Results (SEER) Registry

被引:123
|
作者
Zhang, Jianjun [1 ,2 ]
Gold, Kathryn A. [1 ]
Lin, Heather Y. [3 ]
Swisher, Stephen G. [4 ]
Xing, Yan [5 ]
Lee, J. Jack [3 ]
Kim, Edward S. [6 ]
William, William N., Jr. [1 ]
机构
[1] Univ Texas Houston, MD Anderson Canc Ctr, Dept Thorac Head & Neck Med Oncol, Houston, TX 77030 USA
[2] Univ Texas Houston, MD Anderson Canc Ctr, Dept Genom Med, Houston, TX 77030 USA
[3] Univ Texas Houston, MD Anderson Canc Ctr, Dept Biostat, Houston, TX 77030 USA
[4] Univ Texas Houston, MD Anderson Canc Ctr, Dept Thorac & Cardiovasc Surg, Houston, TX 77030 USA
[5] Harvard Univ, Sch Med, Mt Auburn Hosp, Dept Med, Cambridge, MA 02138 USA
[6] Carolina HealthCare Syst, Levine Canc Inst, Charlotte, NC USA
基金
美国国家卫生研究院;
关键词
Non-small-cell lung cancer; Tumor size; Survival; SEER; FORTHCOMING 7TH EDITION; GROWTH-FACTOR RECEPTOR; TNM CLASSIFICATION; STAGE-I; PROGNOSTIC-FACTORS; CM; IMPACT; PROPOSALS; REVISION; PROJECT;
D O I
10.1097/JTO.0000000000000456
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Introduction: Tumor size is a known prognostic factor for early stage non-small-cell lung cancer (NSCLC), but its significance in node-positive and locally invasive NSCLC has not been extensively characterized. We queried the Surveillance, Epidemiology, and End Results database to evaluate the prognostic value of tumor size for early stage and node-positive and locally invasive NSCLC. Methods: Patients in Surveillance, Epidemiology, and End Results registry with NSCLC diagnosed between 1998 and 2003 were analyzed. Tumor size was analyzed as a continuous variable. Other demographic variables included age, gender, race, histology, primary tumor extension, node status, and primary treatment modality (surgery vs. radiation). The Kaplan-Meier method was used to estimate overall survival (OS). Cox proportional hazard model was used to evaluate whether tumor size was an independent prognostic factor. Results: In all, 52,287 eligible patients were subgrouped based on tumor extension and node status. Tumor size had a significant effect on OS in all subgroups defined by tumor extension or node status. In addition, tumor size also had statistically significant effect on OS in 15 of 16 subgroups defined by tumor extension and nodal status after adjustment for other clinical variables. Our model incorporating tumor size had significantly better predictive accuracy than our alternative model without tumor size. Conclusions: Tumor size is an independent prognostic factor, for early stage and node-positive and locally invasive disease. Prediction tools, such as nomograms, incorporating more detailed information not captured in detail by the routine tumor, node, metastasis classification, may improve prediction accuracy of OS in NSCLC.
引用
收藏
页码:682 / 690
页数:9
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