A novel nomogram and prognostic factor for metastatic soft tissue sarcoma survival

被引:0
作者
Han, Dan [1 ]
Li, Bing [2 ]
Xu, Jie [3 ]
Hu, Yajie [3 ]
Chen, Xi [4 ]
Wang, Ruizhi [3 ]
机构
[1] Fudan Univ, Huadong Hosp, Dept Pharm, Shanghai, Peoples R China
[2] Shanghai Univ Tradit Chinese Med TCM, Peoples Hosp 7, Dept Radiol, Shanghai, Peoples R China
[3] Fudan Univ, Huadong Hosp, Dept Radiol, Shanghai, Peoples R China
[4] Fudan Univ, Huadong Hosp, Dept Oncol, Shanghai, Peoples R China
关键词
metastatic soft tissue sarcoma; immune checkpoint inhibitors; nomogram; survival; SEER database; RADIATION-THERAPY; MARITAL-STATUS; OPEN-LABEL; CANCER; STAGE; DIAGNOSIS; CHEMOTHERAPY; MULTICENTER; EXTREMITIES; IPILIMUMAB;
D O I
10.3389/fendo.2024.1371910
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background This study represented the inaugural effort to develop predictive survival nomograms for metastatic soft tissue sarcoma (mSTS) patients in the era of immune checkpoint inhibitors.Method From the Surveillance, Epidemiology, and End Results (SEER) program database, we extracted 3078 eligible patients with mSTS between 2016 and 2022. Kaplan-Meier survival analysis, univariate and multivariable Cox analyses, and univariate and multivariable logistic analyses were conducted. Subsequently, predictive nomograms were constructed. Clinical effectiveness was validated using the area under the curve (AUC), calibration curve, and decision curve analysis (DCA) methods.Results We used the SEER database to include 3078 eligible patients with mSTS between 2016 and 2022. All the eligible patients were randomly allocated in a ratio of 6:4 and stratified into a training group (n = 1846) and a validation group (n = 1232). In the multivariate Cox analysis, age, race, marital status, pathological grade, histologic subtype, surgery, and chemotherapy were identified as independent prognostic factors. These factors were used to construct the nomogram to predict the 1-, 3-, and 5-year OS of mSTS patients. The C-index for the training cohort and the validation cohort was 0.722(95% confidence interval [CI]: 0.708-0.736), and 0.716(95% CI: 0.698-0.734), respectively. The calibration curves for 1-, 3-, and 5-year OS probability demonstrated excellent calibration between the predicted and the actual survival. The AUC values of the nomogram at 1-, 3-, and 5-year were 0.785, 0.767, and 0.757 in the training cohort, 0.773, 0.754, and 0.751 in the validation cohort, respectively. Furthermore, DCA indicated the favorable clinical utility of the nomogram in both cohorts. The risk stratification system was constructed using the established nomogram, which enhanced prediction accuracy, aided clinicians in identifying high-risk patients and informing treatment decisions.Conclusion This study marked the inaugural effort in constructing predictive survival nomograms mSTS patients in the era of immune checkpoint inhibitors. The robustly constructed nomograms, alongside actual outcomes, offered valuable insights to inform follow-up management strategies.
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