ArticleTranslational cancer research2022
Development and validation of an online prognostic nomogram for osteosarcoma after surgery: a retrospective study based on the SEER database and external validation with single-center data.
Article in Translational cancer research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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5 citing papers in PubMed.
- Prognostic nomograms for overall and cancer-specific survival in individuals with large cell neuroendocrine carcinoma: a population-based study.Translational cancer research · 2026Article
- Time-dependent evolution of osteosarcoma recurrence risk across clinical risk stratification and its prognostic value.American journal of cancer research · 2026Article
- Prognosis of surgery and nomogram for patients with IIIA lung squamous cell carcinoma: a propensity score matched SEER database analysis.Journal of thoracic disease · 2025Article
- Cancer-associated Fibroblast-like Cells Promote Osteosarcoma Metastasis by Upregulation of Phosphoserine Aminotransferase 1 and Activation of the mTOR/S6K Pathway.International journal of biological sciences · 2025Article
- Neurotrophic factors as double-edged swords in osteosarcoma: drivers of tumour growth and immune remodelling.Frontiers in immunology · 2025Review
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Abstract
Background: Osteosarcoma is a severe malignancy with relatively low morbidity and significant variation in patient outcomes. Thus the development of predictive models could help clinicians make better-individualized decisions. The present study established a nomogram to predict postoperative survival of osteosarcoma patients using the large population-based Surveillance, Epidemiology, and End Results (SEER) database and validated it with single-center data from an Asian/Chinese population. Methods: Data from osteosarcoma patients who underwent surgery from 2000 to 2016 in the SEER database were obtained and were randomly divided into a training set (n=1,057) and an internal validation set (n=1,057). Data from osteosarcoma patients who underwent surgery in our hospital from 2013 to 2016 were collected as an external validation set (n=65). Univariate and multivariate Cox proportional hazard models were used in the training set to screen for prognostic factors and a nomogram was established to individually predict 1-, 3- and 5-year cancer-specific survival (CSS) and overall survival (OS). The discrimination and calibration ability of the nomogram were evaluated using the Harrell concordance index (C-index), calibration curves and area under the curve (AUC). The clinical utility was evaluated using decision curve analysis (DCA). Results: Predictive nomograms were generated using characteristics including age, pathological subtype, the American Joint Committee on Cancer (AJCC) group-N, AJCC-M, tumor size, and tumor extension for CSS and OS. The C-indexes for the CSS training set, the internal validation set, and the external validation set were 0.731, 0.713, and 0.721, respectively. The C-indexes of OS C-indices were 0.734, 0.706, and 0.719, respectively. The calibration curve suggested that the nomograms were accurate in their predictions and that DCA showed broad clinical benefits. Moreover, the present nomograms exhibited high accuracy (for CSS: AUC =0.871, 0.772, and 0.759 of 1-, 3-, and 5-year; for OS: AUC =0.869, 0.774, and 0.765 of 1-, 3-, and 5-year) versus AJCC-Stage (for CSS: AUC =0.744, 0.670, and 0.671 of 1-, 3-, and 5-year; for OS: AUC =0.721, 0.665, and 0.662 of 1-, 3-, and 5-year). Conclusions: This study developed and validated a prognostic nomogram integrating clinicopathological characteristics for osteosarcoma patients who underwent surgery. This nomogram can provide individual risk assessment for survival.
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