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Time‐dependent and nonlinear effects of prognostic factors in nonmetastatic colorectal cancer
The survival risk following curative surgery for nonmetastatic colorectal cancer (CRC) may be over‐ or underestimated due to a lack of attention to nonlinear effects and violation of the proportional hazards assumption. In this paper, we aimed to detect and interpret the shape of time‐dependent and...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5548888/ https://www.ncbi.nlm.nih.gov/pubmed/28707427 http://dx.doi.org/10.1002/cam4.1116 |
Sumario: | The survival risk following curative surgery for nonmetastatic colorectal cancer (CRC) may be over‐ or underestimated due to a lack of attention to nonlinear effects and violation of the proportional hazards assumption. In this paper, we aimed to detect and interpret the shape of time‐dependent and nonlinear effects to improve the predictive performance of models of prognoses in nonmetastatic CRC patients. Data for nonmetastatic CRC patients diagnosed between 2004 and 2012 were obtained from the Surveillance Epidemiology End Results registry. Time‐dependent and nonlinear effects were tested and plotted. A nonlinear model that used random survival forests was implemented. The estimated 5‐year cancer‐specific death rate was 17.95% (95% CI, 17.70–18.20%). Tumor invasion depth, lymph node status, age at diagnosis, tumor grade, histology and tumor site were significantly associated with cancer‐specific death. Nonlinear and time‐dependent effects on survival were detected. Positive lymph node number had a larger effect per unit of measurement at low values than at high values, whereas age at diagnosis showed the opposite pattern. Moreover, nonproportional hazards were detected for all covariates, indicating that the contributions of these risks to survival outcomes decreased over time. The nonlinear model predicted prognoses more accurately (C‐index: 0.7934, 0.7933–0.7934) than did the Fine and Gray model (C‐index: 0.7550, 0.7510–0.7583). The three‐dimensional cumulative incidence curves derived from nonlinear model were used to identify the change points of the risk trends. It would be useful to implement these findings in treatment plans and follow‐up surveillance in nonmetastatic CRC patients. |
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