The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.
Regression models for relative survival
Abstract
Four approaches to estimating a regression model for relative survival using the method of maximum likelihood are described and compared. The underlying model is an additive hazards model where the total hazard is written as the sum of the known baseline hazard and the excess hazard associated with a diagnosis of cancer. The excess hazards are assumed to be constant within pre‐specified bands of follow‐up. The likelihood can be maximized directly or in the framework of generalized linear models. Minor differences exist due to, for example, the way the data are presented (individual, aggregated or grouped), and in some assumptions (e.g. distributional assumptions). The four approaches are applied to two real data sets and produce very similar estimates even when the assumption of proportional excess hazards is violated. The choice of approach to use in practice can, therefore, be guided by ease of use and availability of software. We recommend using a generalized linear model with a Poisson error structure based on collapsed data using exact survival times. The model can be estimated in any software package that estimates GLMs with user‐defined link functions (including SAS, Stata, S‐plus, and R) and utilizes the theory of generalized linear models for assessing goodness‐of‐fit and studying regression diagnostics. Copyright © 2004 John Wiley & Sons, Ltd.
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Cites
Regression Models and Life-Tables
Cox, D. R. (1972) · Journal of the Royal Statistical Society Series B: Statistical Methodology · doi:10.1111/j.2517-6161.1972.tb00899.x · Cited by 39,793
McCullagh, P., & Nelder, J. A. (1989) · doi:10.1007/978-1-4899-3242-6 · Cited by 16,836
Cited by
Cervantes, F., Dupriez, B., Pereira, A., Passamonti, F., Reilly, J. T., Morra, E., Vannucchi, A. M., Mesa, R. A., Demory, J.-L., Barosi, G., et al. (2009) · Blood · doi:10.1182/blood-2008-07-170449 · Cited by 1,255
Cancer survival in China, 2003–2005: A population‐based study
Zeng, H., Zheng, R., Guo, Y., Zhang, S., Zou, X., Wang, N., Zhang, L., Tang, J., Chen, J., Wei, K., et al. (2015) · International Journal of Cancer · doi:10.1002/ijc.29227 · Cited by 622
Lemos, B. D., Storer, B. E., Iyer, J. G., Phillips, J. L., Bichakjian, C. K., Fang, L. C., Johnson, T. M., Liegeois-Kwon, N. J., Otley, C. C., Paulson, K. G., et al. (2010) · Journal of the American Academy of Dermatology · doi:10.1016/j.jaad.2010.02.056 · Cited by 559
Gatta, G., Botta, L., Sánchez, M. J., Anderson, L. A., Pierannunzio, D., Licitra, L., Hackl, M., Zielonke, N., Oberaigner, W., Van Eycken, E., et al. (2015) · European Journal of Cancer · doi:10.1016/j.ejca.2015.07.043 · Cited by 485
Johnson, L. F., Mossong, J., Dorrington, R. E., Schomaker, M., Hoffmann, C. J., Keiser, O., Fox, M. P., Wood, R., Prozesky, H., Giddy, J., et al. (2013) · PLoS Medicine · doi:10.1371/journal.pmed.1001418 · Cited by 437
Metadata
- Authors
- Dickman, P. W., Sloggett, A., Hills, M., & Hakulinen, T.
- Venue
- Statistics in Medicine
- Publisher
- Wiley
- Published
- 2003-12-18
- Volume
- 23
- Issue
- 1
- Pages
- 51-64
- ISSN
- 0277-6715 (ISSN-L)
- 1097-0258
- OpenAlex
- W2147416239
- Cited by
- 792
- References
- 2
- FWCI
- 7.61
- Type
- journal article
- Language
- en
- Open access
- closed
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