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. 2025 Sep 1;30(1):831.
doi: 10.1186/s40001-025-03114-0.

Development and validation of a nomogram for predicting overall and cancer-specific survival in elderly patients (≥ 65 years) with epithelial ovarian cancer

Affiliations

Development and validation of a nomogram for predicting overall and cancer-specific survival in elderly patients (≥ 65 years) with epithelial ovarian cancer

Mingzi Tan et al. Eur J Med Res. .

Abstract

Background: Current evidence indicates an uptick in both morbidity and mortality rates of epithelial ovarian cancer (EOC) among the elderly (65 year and older) over the past few years. To date, standardized treatment for elderly patients remains undeveloped. This study utilizes the Surveillance, Epidemiology, and End Results (SEER) database to extract relevant clinicopathological data and construct two nomograms aimed at predicting the prognosis of elderly (65 year and older) patients with EOC. This objective is intended to assist clinicians during clinical decision-making and to assist in individualized prognostication and support clinical decision-making of elderly (65 year and older) EOC patient.

Methods: Our analysis screened a total of 22,181 eligible patients, randomly divided into a training cohort (n = 15,529) and validation cohort (n = 6652) at a ratio of 7:3. 64 cases over 65 year old EOC patient were collected for external validation in our hospital. COX and LASSO analyses were used to screen the independent risk factors for overall survival (OS) and cancer-specific survival (CSS) in elderly patients with EOC. The independent risk factors were used to establish a nomogram by using the "rms" package. The predictive and clinical utility of nomograms was assessed using concordance index, area under the curve (AUC), calibration curve, decision curve analysis and external validation. Kaplan-Meier analysis was conducted to further stratify OS and CSS in high and low-risk groups, assessing the nomograms' stratification efficacy.

Results: The AUCs of the training and validation cohort for OS and CSS prediction at 0.5, 1, 3, 5, and 10 years were significantly higher than the American Joint Committee on Cancer (AJCC) staging system (8th edition). Time-dependent AUC analysis from 1 to 10 years confirmed the nomograms' predictive superiority over the AJCC staging system for both OS and CSS in the training and validation cohorts. Compared with the age, AJCC staging system, the DCA curves of the nomogram showed a greater net gain in the training and external validation cohorts. In the external validation group, C-index of nomogram was 0.938 [95% CI 0.888-0.988], which was significantly better than that of stage (0.762) [95% CI 0.693-0.832] and the results showed that the AUC of Nomogram was significantly higher than that of stage at 1, 3, and 5-year OS and CSS. KM analysis showed that the prognosis of the low-risk group was significantly higher than that of the high-risk group. The developed nomograms outperformed the AJCC staging system in predicting both OS and CSS in elderly (65 year and older) EOC patient.

Conclusions: The developed nomograms offer an effective method for predicting the OS and CSS of elderly ovarian cancer patients, aiding clinicians in making personalized survival projections and refining treatment recommendations.

Keywords: Cancer-specific survival; Elderly patients; Epithelial ovarian cancer; Nomogram; Overall survival.

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Conflict of interest statement

Declarations. Ethics approval and consent to participate: All analyses were conducted in accordance with relevant regulations and guidelines. Consent for publication: All authors agree to publish. Competing interests: The authors declare no competing interests.

Figures

Fig. 1
Fig. 1
The research process of the study
Fig. 2
Fig. 2
According to the X-tile selection of cut-off point. A. The optimal cut-off value for age were 71 and 79 years, and the P of KM analysis was < 0.01; the optimal cut-off value of the number of lymph node biopsies was 3–7, and the P of KM analysis was < 0.01; the number of positive lymph nodes The best cut-off value for tumor size were 1 and 2, and the P for KM analysis was < 0.01; the best cut-off value for tumor size was 64–94 mm, and the P for KM analysis was < 0.01. LASSO analysis: B. LASSO analysis used to select 12 prognostic variables associated with OS in elderly OC patients; C. LASSO analysis used to select 12 prognostic variables associated with CSS in elderly OC patients
Fig. 3
Fig. 3
The nomograms for predicting OS and CSS in elderly (> 65 years old) patients with OC at 3, 5, and 10 years, (A) the nomogram for OS prediction in OC patients; (B) the nomogram for CSS prediction in OC patients
Fig. 4
Fig. 4
AUC curves of the nomogram, AJCC stage, grade, and age for OS. AUC curves of the nomogram, AJCC stage, and tumor grade for prognosis prediction at 0.5, 1, 3, 5, and 10 years in the (A) training and (B) validation cohorts. Time-dependent AUC curves of the nomogram and AJCC stage for prognosis prediction at 1–10 years in the (C) training and (D) validation cohorts
Fig. 5
Fig. 5
AUC curves of the nomogram, AJCC stage, tumor grade, and age for CSS. AUC curves of the nomogram, AJCC stage, and grade for prognosis prediction at 0.5, 1, 3, 5, and 10 years in the (A) training and (B) validation cohorts. Time-dependent AUC curves for prognosis prediction at 1–10 years of the nomogram and AJCC stage in the (C) training and (D) validation cohorts
Fig. 6
Fig. 6
Calibration curves for the OS and CSS nomogram. 3-, 5-, and 10-year calibration curves for the OS nomogram in the (A) training and (B) validation cohorts; 3-, 5-, and 10-year calibration curves for the CSS nomogram in the (C) training and (D) validation cohorts
Fig. 7
Fig. 7
DCA curve of the nomogram, age, and AJCC stage for (A, B) OS and (C, D) CSS in the training and validation cohorts. DCA decision curve analysis, AJCC American Joint Commission on Cancer, OS and CSS
Fig. 8
Fig. 8
Kaplan–Meier curves of (A) OS and (B) CSS for risk classification based on the nomogram scores in the training and validation cohorts

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