Clinical characteristics and prognosis of non-small cell lung cancer patients with liver metastasis: A population-based study

被引:6
作者
Wang, Jun-Feng [1 ]
Lu, Hong-Di [1 ]
Wang, Ying [1 ]
Zhang, Rui [1 ]
Li, Xiang [2 ]
Wang, Sheng [1 ,3 ]
机构
[1] Jilin Prov Tumor Hosp, Dept Thorac Oncol 1, Changchun 130021, Jilin, Peoples R China
[2] Jilin Prov Tumor Hosp, Big Data Ctr Clin Res, Changchun 130021, Jilin, Peoples R China
[3] Jilin Prov Tumor Hosp, Dept Thorac Oncol 1, 1018 Huguang St, Changchun 130021, Jilin, Peoples R China
基金
英国科研创新办公室;
关键词
Non-small cell lung cancer; Liver metastasis; Nomogram; Risk classification system; SURVIVAL; GENDER; EPIDEMIOLOGY; NOMOGRAM; SURGERY; THERAPY; NSCLC;
D O I
10.12998/wjcc.v10.i30.10882
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND The presence of liver metastasis (LM) is an independent prognostic factor for shorter survival in non-small cell lung cancer (NSCLC) patients. The median overall survival of patients with involvement of the liver is less than 5 mo. At present, identifying prognostic factors and constructing survival prediction nomogram for NSCLC patients with LM (NSCLC-LM) are highly desirable. AIM To build a forecasting model to predict the survival time of NSCLC-LM patients. METHODS Data on NSCLC-LM patients were collected from the Surveillance, Epidemiology, and End Results database between 2010 and 2018. Joinpoint analysis was used to estimate the incidence trend of NSCLC-LM. Kaplan-Meier curves were constructed to assess survival time. Cox regression was applied to select the independent prognostic predictors of cancer-specific survival (CSS). A nomogram was established and its prognostic performance was evaluated. RESULTS The age-adjusted incidence of NSCLC-LM increased from 22.7 per 1000000 in 2010 to 25.2 in 2013, and then declined to 22.1 in 2018. According to the multivariable Cox regression analysis of the training set, age, marital status, sex, race, histological type, T stage, metastatic pattern, and whether the patient received chemotherapy or not were identified as independent prognostic factors for CSS (P < 0.05) and were further used to construct a nomogram. The C-indices of the training and validation sets were 0.726 and 0.722, respectively. The results of decision curve analyses (DCAs) and calibration curves showed that the nomogram was well-discriminated and had great clinical utility. CONCLUSION We designed a nomogram model and further constructed a novel risk classification system based on easily accessible clinical factors which demonstrated excellent performance to predict the individual CSS of NSCLC-LM patients.
引用
收藏
页码:10882 / 10895
页数:14
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