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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...

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Autores principales: Chi, Sheng‐Qiang, Tian, Yu, Li, Jun, Tong, Dan‐yang, Kong, Xiang‐Xing, Poston, Graeme, Ding, Ke‐Feng, Li, Jing‐Song
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
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
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author Chi, Sheng‐Qiang
Tian, Yu
Li, Jun
Tong, Dan‐yang
Kong, Xiang‐Xing
Poston, Graeme
Ding, Ke‐Feng
Li, Jing‐Song
author_facet Chi, Sheng‐Qiang
Tian, Yu
Li, Jun
Tong, Dan‐yang
Kong, Xiang‐Xing
Poston, Graeme
Ding, Ke‐Feng
Li, Jing‐Song
author_sort Chi, Sheng‐Qiang
collection PubMed
description 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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spelling pubmed-55488882017-08-09 Time‐dependent and nonlinear effects of prognostic factors in nonmetastatic colorectal cancer Chi, Sheng‐Qiang Tian, Yu Li, Jun Tong, Dan‐yang Kong, Xiang‐Xing Poston, Graeme Ding, Ke‐Feng Li, Jing‐Song Cancer Med Clinical Cancer Research 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. John Wiley and Sons Inc. 2017-07-14 /pmc/articles/PMC5548888/ /pubmed/28707427 http://dx.doi.org/10.1002/cam4.1116 Text en © 2017 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Cancer Research
Chi, Sheng‐Qiang
Tian, Yu
Li, Jun
Tong, Dan‐yang
Kong, Xiang‐Xing
Poston, Graeme
Ding, Ke‐Feng
Li, Jing‐Song
Time‐dependent and nonlinear effects of prognostic factors in nonmetastatic colorectal cancer
title Time‐dependent and nonlinear effects of prognostic factors in nonmetastatic colorectal cancer
title_full Time‐dependent and nonlinear effects of prognostic factors in nonmetastatic colorectal cancer
title_fullStr Time‐dependent and nonlinear effects of prognostic factors in nonmetastatic colorectal cancer
title_full_unstemmed Time‐dependent and nonlinear effects of prognostic factors in nonmetastatic colorectal cancer
title_short Time‐dependent and nonlinear effects of prognostic factors in nonmetastatic colorectal cancer
title_sort time‐dependent and nonlinear effects of prognostic factors in nonmetastatic colorectal cancer
topic Clinical Cancer Research
url 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
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