Prognostic nomogram to predict cancer-specific survival with small-cell carcinoma of the prostate: a multi-institutional study

被引:1
作者
Di, Yupeng [1 ]
Song, Jiazhao [1 ]
Song, Zhuo [1 ]
Wang, Yingjie [1 ]
Meng, Lingling [2 ]
机构
[1] PLA, Dept Radiotherapy, Air Force Med Ctr, Beijing, Peoples R China
[2] Peoples Liberat Army Gen Hosp, Dept Radiat Oncol, Sr Dept Oncol, Med Ctr 5, Beijing, Peoples R China
来源
FRONTIERS IN ONCOLOGY | 2024年 / 14卷
关键词
small-cell carcinoma; prostate; nomogram; cancer-specific survival; surveillance epidemiology and end results; BIG DATA; OUTCOMES;
D O I
10.3389/fonc.2024.1349888
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective The aim of this study is to examine the predictive factors for cancer-specific survival (CSS) in patients diagnosed with Small-Cell Carcinoma of the Prostate (SCCP) and to construct a prognostic model. Methods Cases were selected using the Surveillance, Epidemiology, and End Results (SEER) database. The Kaplan-Meier method was utilized to calculate survival rates, while Lasso and Cox regression were employed to analyze prognostic factors. An independent prognostic factor-based nomogram was created to forecast CSS at 12 and 24 months. The model's predictive efficacy was assessed using the consistency index (C-index), calibration curve, and decision curve analysis (DCA) in separate tests. Results Following the analysis of Cox and Lasso regression, age, race, Summary stage, and chemotherapy were determined to be significant risk factors (P < 0.05). In the group of participants who received training, the rate of 12-month CSS was 44.6%, the rate of 24-month CSS was 25.5%, and the median time for CSS was 10.5 months. The C-index for the training cohort was 0.7688 +/- 0.024. As for the validation cohort, it was 0.661 +/- 0.041. According to the nomogram, CSS was accurately predicted and demonstrated consistent and satisfactory predictive performance at both 12 months (87.3% compared to 71.2%) and 24 months (80.4% compared to 71.7%). As shown in the external validation calibration plot, the AUC for 12- and 24-month is 64.6% vs. 56.9% and 87.0% vs. 70.7%, respectively. Based on the calibration plot of the CSS nomogram at both the 12-month and 24-month marks, it can be observed that both the actual values and the nomogram predictions indicate a predominantly stable CSS. When compared to the AJCC staging system, DCA demonstrated a higher level of accuracy in predicting CSS through the use of a nomogram. Conclusion Clinical prognostic factors can be utilized with nomograms to forecast CSS in Small-Cell Carcinoma of the Prostate (SCCP).
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页数:13
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