Accelerated failure time model
In the statistical area of survival analysis, an accelerated failure time model (AFT model) is a parametric model that provides an alternative to the commonly used proportional hazards models. Whereas a proportional hazards model assumes that the effect of a covariate is to multiply the hazard by some constant, an AFT model assumes that the effect of a covariate is to accelerate or decelerate the life course of a disease by some constant. This is especially appealing in a technical context where the 'disease' is a result of some mechanical process with a known sequence of intermediary stages.
Model specification
In full generality, the accelerated failure time model can be specified as
where denotes the joint effect of covariates, typically .[1]
This is satisfied, if the probability density function of the event is taken to be , from which is follows for the survival function that . From this it is easy to see that the moderated life time is distributed such that and the unmoderated life time have the same distribution. Consequently, can be written as
where the last term is distributed as , i.e. independently of . This reduces the accelerated failure time model into regression analysis (typically a linear model) where represents the fixed effects, and represents the noise. Different distributional forms of imply different distributional forms of , i.e. different baseline distributions of the survival time. It is typical of survival-analytic contexts, that many of the observations are censored, i.e. we only know that , not . In fact, the former case represents survival, while the later case represents an event/death/censoring during the follow-up. These right-censored observations can pose technical challenges for estimating the model, if the distribution of is unusual.
The interpretation of in accelerated failure time models is straight forward: E.g. means that everything in the relevant life history of an individual happens twice as fast. For example, if the model concerns the development of a tumor, it means that all of the pre-stages progress twice as fast as for the unexposed individual, implying that the expected time until a clinical disease is 0.5 of the baseline time. However, this does not mean that the hazard function is twice as high - that would be the proportional hazards model.
Statistical issues
Unlike proportional hazards models, in which Cox's semi-parametric proportional hazards model is more widely used than parametric models, AFT models are predominately fully parametric i.e. a probability distribution is specified for . (Buckley and James[2] proposed a semi-parametric AFT but its use is relatively uncommon in applied research; in a 1992 paper, Wei[3] pointed out that the Buckley–James model has no theoretical justification and lacks robustness, and reviewed alternatives.) This can be a problem, if a degree of realistic detail is required for modelling the distribution of a baseline lifetime. Hence, technical developments in this direction would be highly desirable.
Unlike proportional hazards models, the regression parameter estimates from AFT models are robust to omitted covariates. They are also less affected by the choice of probability distribution.[4][5]
The results of AFT models are easily interpreted.[6] For example, the results of a clinical trial with mortality as the endpoint could be interpreted as a certain percentage increase in future life expectancy on the new treatment compared to the control. So a patient could be informed that he would be expected to live (say) 15% longer if he took the new treatment. Hazard ratios can prove harder to explain in layman's terms.
Distributions used in AFT models
The log-logistic distribution provides the most commonly used AFT model. Unlike the Weibull distribution, it can exhibit a non-monotonic hazard function which increases at early times and decreases at later times. It is similar in shape to the log-normal distribution but its cumulative distribution function has a simple closed form, which becomes important computationally when fitting data with censoring. (Namely, for the censored observations one needs the survival function, which is the complement of the cumulative distribution function, i.e. .)
The Weibull distribution (including the exponential distribution as a special case) can be parameterised as either a proportional hazards model or an AFT model, and is the only family of distributions to have this property. The results of fitting a Weibull model can therefore be interpreted in either framework.
Other distributions suitable for AFT models include the log-normal, gamma and inverse Gaussian distributions, although they are less popular than the log-logistic, partly as their cumulative distribution functions do not have a closed form. Finally, the generalized gamma distribution is a three-parameter distribution that includes the Weibull, log-normal and gamma distributions as special cases.
Connection with multistate models
If an event occurs by a constant rate , it is easy to see that multiplying by results in a model that fulfills both proportional hazards and accelerated failure time assumptions. The accelerated failure time model turns out to be the proper generalization of this model for a multistate (time-homogenous) Markov chain. Namely, consider that it is possible for a system to be in any of states at any moment , and let us assume that the transition between these states occurs according to a constant set of rates . (The collection of these rates is known as the transition matrix , also sometimes known as the infinitesimal generator.) It is known[7] that for this model, the matrix of transition probabilities can be calculated as
i.e. by using the matrix exponential, and the time derivative of this is[8]
- </math>
P'(t) = e^{tQ}Q. </math>
The biological interpretation of this is such that if a disease develops as a result of a known sequence of states , and the effect of risk factors accelerates this process linearly, the overall risk of disease per time unit follows an accelerated failure time model, not e.g. a proportional hazards model. Of course, it may be biologically more realistic to assume that scales each of the rates differentially. The resulting model in this case is a hybrid (i.e. neither of the commonly used types), and it is difficult to say anything concerning its properties in full generality.
References
- ^ Kalbfleisch & Prentice (2002). The Statistical Analysis of Failure Time Data (2nd ed.). Hoboken, NJ: Wiley Series in Probability and Statistics.
- ^ Buckley, Jonathan; James, Ian (1979), "Linear regression with censored data", Biometrika, 66 (3): 429–436, doi:10.1093/biomet/66.3.429, JSTOR 2335161
- ^ Attention: This template ({{cite doi}}) is deprecated. To cite the publication identified by doi:10.1002/sim.4780111409, please use {{cite journal}} (if it was published in a bona fide academic journal, otherwise {{cite report}} with
|doi=10.1002/sim.4780111409
instead. - ^ Lambert, Philippe; Collett, Dave; Kimber, Alan; Johnson, Rachel (2004), "Parametric accelerated failure time models with random effects and an application to kidney transplant survival", Statistics in Medicine, 23 (20): 3177–3192, doi:10.1002/sim.1876, PMID 15449337
- ^ Template:Cite doi/10.1002.2F.28SICI.291097-0258.2819970130.2916:2.3C215::AID-SIM481.3E3.0.CO.3B2-J
- ^ Kay, Richard; Kinnersley, Nelson (2002), "On the use of the accelerated failure time model as an alternative to the proportional hazards model in the treatment of time to event data: A case study in influenza", Drug Information Journal, 36 (3): 571–579
- ^ Norris, J.R. (1997). Markov Chains. Cambridge: Cambridge University Press.
- ^ Norris, J.R. (1997). Markov Chains. Cambridge: Cambridge University Press.
Further reading
- Bradburn, MJ; Clark, TG; Love, SB; Altman, DG (2003), "Survival Analysis Part II: Multivariate data analysis - an introduction to concepts and methods", British Journal of Cancer, 89 (89): 431–436, doi:10.1038/sj.bjc.6601119, PMC 2394368, PMID 12888808
- Hougaard, Philip (1999), "Fundamentals of Survival Data", Biometrics, 55 (1): 13–22, doi:10.1111/j.0006-341X.1999.00013.x, PMID 11318147
- Collett, D. (2003), Modelling Survival Data in Medical Research (2nd ed.), CRC press, ISBN 1-58488-325-1
- Cox, David Roxbee; Oakes, D. (1984), Analysis of Survival Data, CRC Press, ISBN 0-412-24490-X
- Marubini, Ettore; Valsecchi, Maria Grazia (1995), Analysing Survival Data from Clinical Trials and Observational Studies, Wiley, ISBN 0-470-09341-2
- Martinussen, Torben; Scheike, Thomas (2006), Dynamic Regression Models for Survival Data, Springer, ISBN 0-387-20274-9
- Bagdonavicius, Vilijandas; Nikulin, Mikhail (2002), Accelerated Life Models. Modeling and Statistical Analysis, Chapman&Hall/CRC, ISBN 1-58488-186-0