Adaptively Identifying Patient Populations With Treatment Benefit in Clinical Trials

08/11/2022
by   Alicia Curth, et al.
8

We study the problem of adaptively identifying patient subpopulations that benefit from a given treatment during a confirmatory clinical trial. This type of adaptive clinical trial, often referred to as adaptive enrichment design, has been thoroughly studied in biostatistics with a focus on a limited number of subgroups (typically two) which make up (sub)populations, and a small number of interim analysis points. In this paper, we aim to relax classical restrictions on such designs and investigate how to incorporate ideas from the recent machine learning literature on adaptive and online experimentation to make trials more flexible and efficient. We find that the unique characteristics of the subpopulation selection problem – most importantly that (i) one is usually interested in finding subpopulations with any treatment benefit (and not necessarily the single subgroup with largest effect) given a limited budget and that (ii) effectiveness only has to be demonstrated across the subpopulation on average – give rise to interesting challenges and new desiderata when designing algorithmic solutions. Building on these findings, we propose AdaGGI and AdaGCPI, two meta-algorithms for subpopulation construction, which focus on identifying good subgroups and good composite subpopulations, respectively. We empirically investigate their performance across a range of simulation scenarios and derive insights into their (dis)advantages across different settings.

READ FULL TEXT

page 1

page 2

page 3

page 4

research
10/30/2018

Recent advances in methodology for clinical trials in small populations: the InSPiRe project

Where there are a limited number of patients, such as in a rare disease,...
research
11/03/2019

Bayesian adaptive N-of-1 trials for estimating population and individual treatment effects

This article presents a novel adaptive design algorithm that can be used...
research
01/08/2020

Contextual Constrained Learning for Dose-Finding Clinical Trials

Clinical trials in the medical domain are constrained by budgets. The nu...
research
03/26/2021

Leveraging Historical Data for High-Dimensional Regression Adjustment, a Composite Covariate Approach

The amount of data collected from patients involved in clinical trials i...
research
07/09/2019

Making Study Populations Visible through Knowledge Graphs

Treatment recommendations within Clinical Practice Guidelines (CPGs) are...
research
11/23/2019

Doctor2Vec: Dynamic Doctor Representation Learning for Clinical Trial Recruitment

Massive electronic health records (EHRs) enable the success of learning ...
research
08/08/2022

Sensitivity Analyses of Clinical Trial Designs: Selecting Scenarios and Summarizing Operating Characteristics

The use of simulation-based sensitivity analyses is fundamental to evalu...

Please sign up or login with your details

Forgot password? Click here to reset