期刊
JOURNAL OF CANCER
卷 12, 期 23, 页码 7223-7236出版社
IVYSPRING INT PUBL
DOI: 10.7150/jca.63224
关键词
Ovarian carcinosarcoma; Nomogram; Overall survival; Cancer-specific survival; Validation
类别
资金
- 345 Talent Project of Shengjing Hospital
This study aimed to construct nomograms using data from the SEER database to predict overall survival and cancer-specific survival of ovarian carcinosarcoma (OCS) patients. The nomograms based on independent prognostic factors showed good predictive power and clinical practicality, outperforming traditional staging and grading systems. They enable personalized evaluation of OS and CSS, guiding treatment decisions.
Background: At present, there is no clinical prediction model for ovarian carcinosarcoma (OCS) that is based on a large sample of real data. This study aimed to construct nomograms using data extracted from the Surveillance, Epidemiology, and End Results (SEER) database that can be used to predict the overall survival (OS) and cancer-specific survival (CSS) of patients with OCS and further guide the choice of clinical treatment. Methods: We selected 2753 cases of OCS from the SEER database from 1998 to 2016. Patients were randomly divided in a 7:3 ratio into a training cohort (n = 1929) and a validation cohort (n = 824). Cox analysis was used to select prognostic factors for OS and CSS, and nomograms were then established. The performance of nomogram models was assessed using the concordance index, the area under the receiver operating characteristic curve, calibration curves, and by decision curve analysis. Data from 21 OCS patients at Shengjing Hospital from 2001 to 2021 were collected for external verification. Kaplan-Meier curves were plotted to compare survival outcomes between subgroups. Results: Nomograms based on independent prognostic factors showed good predictive power and clinical practicality. Internal and external validation indicated that the nomograms performed better than staging and grading systems. Significant differences were observed in the survival curves of different risk subgroups. Conclusions: The developed nomograms will enable individualized evaluation of the OS and CSS, thus guiding the treatment of patients with OCS.
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