Working Paper: NBER ID: w31305
Authors: Charles F. Manski
Abstract: In medical treatment and elsewhere, it has become standard to base treatment intensity (dosage) on evidence in randomized trials. Yet it has been rare to study how outcomes vary with dosage. In trials to obtain drug approval, the norm has been to specify some dose of a new drug and compare it with an established therapy or placebo. Design-based trial analysis views each trial arm as qualitatively different, but it may be highly credible to assume that efficacy and adverse effects (AEs) weakly increase with dosage. Optimization of patient care requires joint attention to both, as well as to treatment cost. This paper develops methodology to credibly use limited trial evidence to choose dosage when efficacy and AEs weakly increase with dose. I suppose that dosage is an integer choice t ∊ (0, 1, . . . , T), T being a specified maximum dose. I study dosage choice when trial evidence on outcomes is available for only K dose levels, where K < T + 1. Then the population distribution of dose response is partially rather than point identified. The identification region is a convex polygon determined by linear equalities and inequalities. I characterize clinical and public-health decision making using the minimax-regret criterion. A simple analytical solution exists when T = 2 and computation is tractable when T is larger.
Keywords: treatment dosage; efficacy; adverse effects; medical trials; decision-making
JEL Codes: C44; I1
Edges that are evidenced by causal inference methods are in orange, and the rest are in light blue.
| Cause | Effect |
|---|---|
| dosage (t) (Y20) | efficacy (e) (I20) |
| dosage (t) (Y20) | adverse effects (AEs) (a) (I12) |
| efficacy (e) (I20) | risk of disease recurrence (I12) |
| adverse effects (AEs) (a) (I12) | risk of disease recurrence (I12) |