Regression models for relative survival

被引:666
作者
Dickman, PW
Sloggett, A
Hills, M
Hakulinen, T
机构
[1] Karolinska Inst, Dept Med Epidemiol, S-17177 Stockholm, Sweden
[2] London Sch Hyg & Trop Med, London WC1, England
[3] Finnish Canc Registry, FIN-00170 Helsinki, Finland
[4] Univ Helsinki, Dept Publ Hlth, Helsinki, Finland
关键词
relative survival; excess mortality; net survival; cancer; registry; regression;
D O I
10.1002/sim.1597
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 (C) 2004 John Wiley Sons, Ltd.
引用
收藏
页码:51 / 64
页数:14
相关论文
共 29 条
[1]  
Andersen PK., 1995, Statistical Models Based on Counting Processes
[2]  
[Anonymous], 1987, Statistical methods in cancer research, Vol 1-The analysis of case-control studies
[3]  
BERKSON J, 1950, P STAFF M MAYO CLIN, V25, P270
[4]  
BERRINO F, 1999, IARC SCI PUBLICATION, V151
[5]   Modelling time-dependent hazard ratios in relative survival: Application to colon cancer [J].
Bolard, P ;
Quantin, C ;
Esteve, J ;
Faivre, J ;
Abrahamowicz, M .
JOURNAL OF CLINICAL EPIDEMIOLOGY, 2001, 54 (10) :986-996
[6]   Up-to-date long-term survival curves of patients with cancer by period analysis [J].
Brenner, H ;
Hakulinen, T .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (03) :826-832
[7]  
Brenner H, 1996, CANCER-AM CANCER SOC, V78, P2004, DOI 10.1002/(SICI)1097-0142(19961101)78:9<2004::AID-CNCR23>3.3.CO
[8]  
2-6
[9]   ADDITIVE AND MULTIPLICATIVE MODELS FOR RELATIVE SURVIVAL RATES [J].
BUCKLEY, JD .
BIOMETRICS, 1984, 40 (01) :51-62
[10]  
Bull K, 1997, STAT MED, V16, P1041