Development and validation of machine learning nomograms for predicting survival in stage IV pancreatic cancer: A retrospective study.
1/5 보강
PICO 자동 추출 (휴리스틱, conf 2/4)
유사 논문P · Population 대상 환자/모집단
The Surveillance, Epidemiology, and End Results (SEER) database offers a valuable resource for studying large patient cohorts, yet machine learning-based nomograms for stage IV PC prognosis remain underexplored.
I · Intervention 중재 / 시술
추출되지 않음
C · Comparison 대조 / 비교
추출되지 않음
O · Outcome 결과 / 결론
Calibration curves demonstrated excellent model accuracy. [CONCLUSION] The nomogram developed using age, grade, chemotherapy, surgery, and liver metastasis as predictors can reliably estimate survival outcomes for stage IV PC patients and offers a potential tool for individualized clinical decision-making.
[BACKGROUND] Stage IV pancreatic cancer (PC) has a poor prognosis and lacks individualized prognostic tools.
- 추적기간 4 months
APA
Huang K, Chen Z, et al. (2025). Development and validation of machine learning nomograms for predicting survival in stage IV pancreatic cancer: A retrospective study.. World journal of gastrointestinal oncology, 17(5), 102459. https://doi.org/10.4251/wjgo.v17.i5.102459
MLA
Huang K, et al.. "Development and validation of machine learning nomograms for predicting survival in stage IV pancreatic cancer: A retrospective study.." World journal of gastrointestinal oncology, vol. 17, no. 5, 2025, pp. 102459.
PMID
40487945 ↗
Abstract 한글 요약
[BACKGROUND] Stage IV pancreatic cancer (PC) has a poor prognosis and lacks individualized prognostic tools. Current survival prediction models are limited, and there is a need for more accurate, personalized methods. The Surveillance, Epidemiology, and End Results (SEER) database offers a valuable resource for studying large patient cohorts, yet machine learning-based nomograms for stage IV PC prognosis remain underexplored. This study hypothesizes that a machine learning-based nomogram can predict cancer-specific survival (CSS) and overall survival (OS) with high accuracy in stage IV PC patients.
[AIM] To construct and validate a machine learning-based nomogram for predicting survival in stage IV PC patients using real-world data.
[METHODS] Clinical data from stage IV PC patients diagnosed pathology from 2000 to 2019 were extracted from the SEER database. Patients were randomly divided into a training set and a validation set in a 7:3 ratio. Multivariate Cox proportional hazards, Least Absolute Shrinkage and Selection Operator regression, and Random Survival Forest models were used to identify prognostic variables. A nomogram was constructed to predict CSS and OS at 6, 12, and 18 months. The C-index, receiver operating characteristic curves, and calibration curves were used to evaluate the model's predictive performance.
[RESULTS] A total of 1662 patients were included (1163 in the training set, 499 in the validation set). The median follow-up times were 4 months [interquartile range (IQR): 1-10 months] for the training set and 4 months (IQR: 1-11 months) for the validation set. Key independent prognostic factors identified included age, race, marital status, tumor location, N stage, grade, surgery, chemotherapy, and liver metastasis. The nomogram accurately predicted OS and CSS at 6, 12, and 18 months, with a C-index of 0.727 (OS) and 0.727 (CSS) in the training set, and 0.719 (OS) and 0.716 (CSS) in the validation set. Calibration curves demonstrated excellent model accuracy.
[CONCLUSION] The nomogram developed using age, grade, chemotherapy, surgery, and liver metastasis as predictors can reliably estimate survival outcomes for stage IV PC patients and offers a potential tool for individualized clinical decision-making.
[AIM] To construct and validate a machine learning-based nomogram for predicting survival in stage IV PC patients using real-world data.
[METHODS] Clinical data from stage IV PC patients diagnosed pathology from 2000 to 2019 were extracted from the SEER database. Patients were randomly divided into a training set and a validation set in a 7:3 ratio. Multivariate Cox proportional hazards, Least Absolute Shrinkage and Selection Operator regression, and Random Survival Forest models were used to identify prognostic variables. A nomogram was constructed to predict CSS and OS at 6, 12, and 18 months. The C-index, receiver operating characteristic curves, and calibration curves were used to evaluate the model's predictive performance.
[RESULTS] A total of 1662 patients were included (1163 in the training set, 499 in the validation set). The median follow-up times were 4 months [interquartile range (IQR): 1-10 months] for the training set and 4 months (IQR: 1-11 months) for the validation set. Key independent prognostic factors identified included age, race, marital status, tumor location, N stage, grade, surgery, chemotherapy, and liver metastasis. The nomogram accurately predicted OS and CSS at 6, 12, and 18 months, with a C-index of 0.727 (OS) and 0.727 (CSS) in the training set, and 0.719 (OS) and 0.716 (CSS) in the validation set. Calibration curves demonstrated excellent model accuracy.
[CONCLUSION] The nomogram developed using age, grade, chemotherapy, surgery, and liver metastasis as predictors can reliably estimate survival outcomes for stage IV PC patients and offers a potential tool for individualized clinical decision-making.
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