The study was supported by grants from the Medical Science &#38; Technology Plan Project of Zhejiang Province (grant numbers 2013KYA212), the general program of Zhejiang Province Natural Science Foundation (grant number Y19H160126), and the key program of the Jinhua Municipal Science &#38; Technology Bureau (grant number 2016-3-005, 2018-3-001d, and 2019-3-013).

The Surveillance, Epidemiology, and End Results (SEER) database is an open-access cancer database that only contains deidentified patient data (SEER ID: 12296-Nov2018). Therefore, this study was exempted from the approval of the review board of the Affiliated Jinhua Hospital, Zhejiang University School of Medicine.
1. Data preparation and R packages preparation
<ol>
	<li>Prepare and import the data. 
	&#62; Dataset &#60;- read.csv(&#34;&#8230;/Breast cancer Data.xls...

<ol>
	<li>Andersen, P. K., Gill, R. D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Cox's+regression+model+for+counting+processes:+A+large+sample+study.">Cox's regression model for counting processes: A large sample study.</a> The Annals of Statistics. 10 (4), 1100-1120 (1982).</li><li>Lubsen, J., Pool, J., vander Does, E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+practical+device+for+the+application+of+a+diagnostic+or+prognostic+function.">A practical device for the application of a diagnostic or prognostic function.</a> Methods of Information in Medicine. 17 (2), 127-129 (1978).</li><li>Harrell, F. E., Lee, K. L., Mark, D. B. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Multivariable+prognostic+models:+Issues+in+developing+models,+evaluating+assumptions+and+adequacy,+and+measuring+and+reducing+errors.">Multivariable prognostic models: Issues in developing models, evaluating assumptions and adequacy, and measuring and reducing errors.</a> Statistics In Medicine. 15 (4), 361-387 (1996).</li><li>Hung, H., Chiang, C. -. T. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Estimation+methods+for+time-dependent+AUC+models+with+survival+data.">Estimation methods for time-dependent AUC models with survival data.</a> The Canadian Journal of Statistics / La Revue Canadienne de Statistique. 38 (1), 8-26 (2010).</li><li>Moons, K. G. M., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Risk+prediction+models:+I.+Development,+internal+validation,+and+assessing+the+incremental+value+of+a+new+(bio)marker.">Risk prediction models: I. Development, internal validation, and assessing the incremental value of a new (bio)marker.</a> Heart. 98 (9), 683-690 (2012).</li><li>Fu, J., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Real-world+impact+of+non-breast+cancer-specific+death+on+overall+survival+in+resectable+breast+cancer.">Real-world impact of non-breast cancer-specific death on overall survival in resectable breast cancer.</a> Cancer. 123 (13), 2432-2443 (2017).</li><li>Fine, J. P., Gray, R. J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+proportional+hazards+model+for+the+subdistribution+of+a+competing+risk.">A proportional hazards model for the subdistribution of a competing risk.</a> Journal of the American Statistical Association. 94 (446), 496-509 (1999).</li><li>Wu, L., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Establishing+a+competing+risk+regression+nomogram+model+for+survival+data.">Establishing a competing risk regression nomogram model for survival data.</a> Journal of Visualized Experiments. (164), e60684 (2020).</li><li>Zhang, Z., Geskus, R. B., Kattan, M. W., Zhang, H., Liu, T. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Nomogram+for+survival+analysis+in+the+presence+of+competing+risks.">Nomogram for survival analysis in the presence of competing risks.</a> Annals of Translational Medicine. 5 (20), 403 (2017).</li><li>Zhang, Z. H., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Overview+of+model+validation+for+survival+regression+model+with+competing+risks+using+melanoma+study+data.">Overview of model validation for survival regression model with competing risks using melanoma study data.</a> Annals Of Translational Medicine. 6 (16), 325 (2018).</li><li>Newson, R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Confidence+intervals+for+rank+statistics:+Somers'+D+and+extensions.">Confidence intervals for rank statistics: Somers' D and extensions.</a> Stata Journal. 6 (3), 309-334 (2006).</li><li>Davison, A. C., Hinkley, D. V., Schechtman, E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Efficient+bootstrap+simulation.">Efficient bootstrap simulation.</a> Biometrika. 73 (3), 555-566 (1986).</li><li>Roecker, E. B. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Prediction+error+and+its+estimation+for+subset-selected+models.">Prediction error and its estimation for subset-selected models.</a> Technometrics. 33 (4), 459-468 (1991).</li><li>Steyerberg, E. W., Harrell, F. 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This study compared competing risk nomograms established by two distinct methods and conducted evaluation and validation of the established nomograms. Specifically, this study provided a step-by-step tutorial for establishing the nomogram based on a direct method, as well as calculating the C-index and plotting the calibration curves.
The rms package in R software is widely used for the construction and evaluation of Cox proportional hazard models, but it is not applicable for competi...

In recent years, emerging prognostic factors have been identified with the development of precision medicine, and prognostic models combining molecular and clinicopathological factors are drawing increasing attention in clinical settings. However, non-graphical models, such as the Cox proportional hazard model, with results of coefficient values, are difficult for clinicians to understand1. In comparison, a nomogram is a visualization tool of regression models (including the Cox regression model, competing risk model, etc.), a two-dimensional diagram designed for the approximate graphical computation of a mathematical function2. It enables the valuation of different levels of variables in a clinical model and the calculation of risk scores (RS) to predict prognosis.
Model evaluation is essential in model construction, and two characteristics are generally accepted for evaluation: discrimination and calibration. In clinical models, discrimination refers to the ability of a model to separate individuals who develop events from those who do not, such as patients who die versus those who remain alive, and the concordance index (C-index) or the area under the receiver operating characteristic curve (AUC) are typically used to characterize it3,4. Calibration is a process of comparing the predicted probabilities of a model with the actual probabilities, and calibration curves have been widely used to represent it. In addition, model validation (internal and external validation) is an important step in model construction, and only validated models can be further extrapolated5.
The Cox proportional hazard model is a regression model used in medical research for investigating the associations between prognostic factors and survival status. However, the Cox proportional hazard model only considers two statuses of outcome [Y (0, 1)], while study subjects often face more than two statuses, and competing risks arise [Y (0, 1, 2)]1. Overall survival (OS), which is defined as the time from the date of origin (e.g., treatment) to the date of death due to any cause, is the most important endpoint in survival analysis. However, the OS fails to differentiate cancer-specific death from non-cancer-specific death (e.g., cardiovascular events and other unrelated causes), thus ignoring competing risks6. In these situations, the competing risk model is preferred for the prediction of survival status with the consideration of competing risks7. The methodology of constructing and validating Cox proportional hazard models is well-established, while there have been few reports regarding the validation of competing risk models.
In our previous study, a specific competing risk nomogram, a combination of a nomogram and competing risk model, and a risk score estimation based on a competing risk model were established8. This study aims to present different methods of evaluation and validation of the established competing risk nomogram, which should serve as a useful tool for clinicians to predict prognosis with the consideration of competing risks.

<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>R software</td>
			<td>None</td>
			<td>Not Applicable</td>
			<td>Version 3.6.2 or higher&#160;</td>
		</tr>
		<tr>
			<td>Computer system</td>
			<td>Microsoft&#160;</td>
			<td>Windows 10</td>
			<td>&#160;Windows 10 or higher</td>
		</tr>
	</tbody>
</table>

an r-based landscape validation of a competing risk model

The Cox proportional hazard model is widely applied for survival analyses in clinical settings, but it is not able to cope with multiple survival outcomes. Different from the traditional Cox proportional hazard model, competing risk models consider the presence of competing events and their combination with a nomogram, a graphical calculating device, which is a useful tool for clinicians to conduct a precise prognostic prediction. In this study, we report a method for establishing the competing risk nomogram, that is, the evaluation of its discrimination (i.e., concordance index and area under the curve) and calibration (i.e., calibration curves) abilities, as well as the net benefit (i.e., decision curve analysis). In addition, internal validation using bootstrap resamples of the original dataset and external validation using an external dataset of the established competing risk nomogram were also performed to demonstrate its extrapolation ability. The competing risk nomogram should serve as a useful tool for clinicians to predict prognosis with the consideration of competing risks.

In this study, data of patients with breast cancer were retrieved from the SEER database and served as example data. The SEER database provides data on cancer representing around 34.6% of the United States population, and permission to access the database was obtained (reference number 12296-Nov2018).
Two nomograms (Figure 1), both including histological type, differentiated grade, T stage, and N stage, were established using the direct method and the weighted met...

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An R-Based Landscape Validation of a Competing Risk Model

The present protocol describes codes in R for evaluating the discrimination and calibration abilities of a competing risk model, as well as codes for the internal and external validation of it.

The Cox proportional hazard model is widely applied for survival analyses in clinical settings, but it is not able to cope with multiple survival ...

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1.8K vistas.  Zhejiang University School of Medicine. Nuestro protocolo presenta diferentes métodos de evaluación y validación del nomograma de riesgo competitivo; que considera la presencia de eventos competitivos en el análisis de supervivencia. Este protocolo sirve como complemento al paquete de regresión de riesgo en R.Como el cálculo del índice C y la validación interna, utilizando el método bootstrap. Para comenzar con la discriminación de índice C, ajuste la mazorca de matriz en el modelo de riesgo competidor mod CRR y obtenga ...