Dynamic treatment regimes (DTRs) operationalize the clinical decision process as a sequence of functions, one for each clinical decision, where each function maps up-to-date patient information to a single recommended treatment. Current methods for estimating optimal DTRs, for example Q-learning, require the specification of a single outcome by which the goodness of competing dynamic treatment regimes is measured. However, this is an over-simplification of the goal of clinical decision making, which aims to balance several potentially competing outcomes, for example, symptom relief and side-effect burden. When there are competing outcomes and patients do not know or cannot communicate their preferences, formation of a single composite outcome that correctly balances the competing outcomes is not possible. This problem also occurs when patient preferences evolve over time. We propose a method for constructing DTRs that accommodates competing outcomes by recommending sets of treatments at each decision point. Formally, we construct a sequence of set-valued functions that take as input up-to-date patient information and give as output a recommended subset of the possible treatments. For a given patient history, the recommended set of treatments contains all treatments that produce non-inferior outcome vectors. Constructing these set-valued functions requires solving a non-trivial enumeration problem. We offer an exact enumeration algorithm by recasting the problem as a linear mixed integer program. The proposed methods are illustrated using data from the CATIE schizophrenia study.
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Univ Western Ontario, Dept Stat & Actuarial Sci, London, ON, CanadaUniv Western Ontario, Dept Stat & Actuarial Sci, London, ON, Canada
Charvadeh, Yasin Khadem
Yi, Grace Y.
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Univ Western Ontario, Dept Stat & Actuarial Sci, London, ON, Canada
Univ Western Ontario, Dept Comp Sci, London, ON, Canada
Univ Western Ontario, Dept Stat & Actuarial Sci, Dept Comp Sci, 1151 Richmond St, London, ON N6A 5B7, CanadaUniv Western Ontario, Dept Stat & Actuarial Sci, London, ON, Canada
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Harvard Univ, Sch Publ Hlth, Boston, MA 02115 USAHarvard Univ, Sch Publ Hlth, Boston, MA 02115 USA
Cain, Lauren E.
Robins, James M.
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Harvard Univ, Sch Publ Hlth, Boston, MA 02115 USAHarvard Univ, Sch Publ Hlth, Boston, MA 02115 USA
Robins, James M.
Lanoy, Emilie
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INSERM, U943, Paris, FranceHarvard Univ, Sch Publ Hlth, Boston, MA 02115 USA
Lanoy, Emilie
Logan, Roger
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Harvard Univ, Sch Publ Hlth, Boston, MA 02115 USAHarvard Univ, Sch Publ Hlth, Boston, MA 02115 USA
Logan, Roger
Costagliola, Dominique
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INSERM, U943, Paris, France
Univ Paris 06, Paris, FranceHarvard Univ, Sch Publ Hlth, Boston, MA 02115 USA
Costagliola, Dominique
Hernan, Miguel A.
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Harvard Univ, Sch Publ Hlth, Boston, MA 02115 USA
Harvard MIT Div Hlth Sci & Technol, Cambridge, MA USAHarvard Univ, Sch Publ Hlth, Boston, MA 02115 USA