Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2008 May 10;27(10):1626-45.
doi: 10.1002/sim.3039.

Sequential causal inference: application to randomized trials of adaptive treatment strategies

Affiliations

Sequential causal inference: application to randomized trials of adaptive treatment strategies

Ree Dawson et al. Stat Med. .

Abstract

Clinical trials that randomize subjects to decision algorithms, which adapt treatments over time according to individual response, have gained considerable interest as investigators seek designs that directly inform clinical decision making. We consider designs in which subjects are randomized sequentially at decision points, among adaptive treatment options under evaluation. We present a sequential method to estimate the comparative effects of the randomized adaptive treatments, which are formalized as adaptive treatment strategies. Our causal estimators are derived using Bayesian predictive inference. We use analytical and empirical calculations to compare the predictive estimators to (i) the 'standard' approach that allocates the sequentially obtained data to separate strategy-specific groups as would arise from randomizing subjects at baseline; (ii) the semi-parametric approach of marginal mean models that, under appropriate experimental conditions, provides the same sequential estimator of causal differences as the proposed approach. Simulation studies demonstrate that sequential causal inference offers substantial efficiency gains over the standard approach to comparing treatments, because the predictive estimators can take advantage of the monotone structure of shared data among adaptive strategies. We further demonstrate that the semi-parametric asymptotic variances, which are marginal 'one-step' estimators, may exhibit significant bias, in contrast to the predictive variances. We show that the conditions under which the sequential method is attractive relative to the other two approaches are those most likely to occur in real studies.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Lavori PW, Dawson R. Dynamic treatment regimes: practical design considerations. Clinical Trials. 2004;1:9–20. - PubMed
    1. Murphy S. An experimental design for the development of adaptive treatment strategies. Statistics in Medicine. 2005;24:1455–1481. - PubMed
    1. Thall PF, Millikan RE, Sung HG. Evaluating multiple treatment courses in clinical trials. Statistics in Medicine. 2000;19:1011–1028. - PubMed
    1. Schneider LS, Tariot PN, Lyketsos CG, Dagerman KS, Davis KL, Davis S, Hsiao JK, Jeste DV, Katz IR, Olin JT, Pollock BG, Rabins PV, Rosenheck RA, Small GW, Lebowitz B, Lieberman JA. National Institute of Mental Health Clinical Antipsychotic Trials of Intervention Effectiveness (CATIE): Alzheimer disease trial methodology. American Journal of Geriatric Psychiatry. 2001;9:346–360. - PubMed
    1. Brooner RK, Kidorf M. Using behavioral reinforcement to improve methadone treatment participation. Science and Practice Perspectives. 2002;1:38–48. - PMC - PubMed

Publication types

LinkOut - more resources