Design and estimation in clinical trials with subpopulation selection

Type: Article

Publication Date: 2018-08-07

Citations: 24

DOI: https://doi.org/10.1002/sim.7925

Abstract

Population heterogeneity is frequently observed among patients' treatment responses in clinical trials because of various factors such as clinical background, environmental, and genetic factors. Different subpopulations defined by those baseline factors can lead to differences in the benefit or safety profile of a therapeutic intervention. Ignoring heterogeneity between subpopulations can substantially impact on medical practice. One approach to address heterogeneity necessitates designs and analysis of clinical trials with subpopulation selection. Several types of designs have been proposed for different circumstances. In this work, we discuss a class of designs that allow selection of a predefined subgroup. Using the selection based on the maximum test statistics as the worst-case scenario, we then investigate the precision and accuracy of the maximum likelihood estimator at the end of the study via simulations. We find that the required sample size is chiefly determined by the subgroup prevalence and show in simulations that the maximum likelihood estimator for these designs can be substantially biased.

Locations

  • PubMed Central - View
  • Europe PMC (PubMed Central) - View - PDF
  • Lancaster EPrints (Lancaster University) - View - PDF
  • PubMed - View
  • Statistics in Medicine - View - PDF

Similar Works

Action Title Year Authors
+ PDF Chat Estimation of treatment effect in a subpopulation: An empirical Bayes approach 2015 Changyu Shen
Xiaochun Li
Jaesik Jeong
+ Practical Considerations for Subgroups Quantification, Selection and Adaptive Enrichment in Confirmatory Trials 2019 Jianchang Lin
Veronica Bunn
Rachael Liu
+ Design and Analysis Considerations in Clinical Trials With a Sensitive Subpopulation 2010 Yan Zhao
Alex Dmitrienko
Roy Tamura
+ A Framework of Statistical Methods for Identification of Subgroups with Differential Treatment Effects in Randomized Trials 2015 Lei Shen
Ying Ding
Chakib Battioui
+ PDF Chat Comparing Approaches to Treatment Effect Estimation for Subgroups in Clinical Trials 2016 Marius Thomas
Björn Bornkamp
+ PDF Chat Phase II Trials for Heterogeneous Patient Populations with a Time-to-Event Endpoint 2017 Sin‐Ho Jung
+ Logical Inference on Treatment Efficacy When Subgroups Exist 2020 Ying Ding
Wei Yue
Xinjun Wang
+ Assessment of Methods to Identify Patient Subgroups with Enhanced Treatment Response in Randomized Clinical Trials 2015 Richard C. Zink
Lei Shen
Russell D. Wolfinger
Hollins Showalter
+ Statistical design considerations for trials that study multiple indications 2020 Alexander Kaizer
Joseph S. Koopmeiners
Nan Chen
Brian P. Hobbs
+ Statistical design considerations for trials that study multiple indications 2020 Alexander Kaizer
Joseph S. Koopmeiners
Nan Chen
Brian P. Hobbs
+ Statistical design considerations for trials that study multiple indications 2020 Alexander Kaizer
Joseph S. Koopmeiners
Nan Chen
Brian P. Hobbs
+ Comparing algorithms for characterizing treatment effect heterogeneity in randomized trials 2022 Sophie Sun
Konstantinos Sechidis
Yao Chen
Jiarui Lu
Chong Ma
Ardalan Mirshani
David Ohlssen
Marc Vandemeulebroecke
Björn Bornkamp
+ PDF Chat Bayesian Approaches to Subgroup Analysis and Related Adaptive Clinical Trial Designs 2019 Ciara Nugent
Wentian Guo
Peter Müller
Yuan Ji
+ Identification of biomarker-defined populations in precision medicine 2023 Cynthia Huber
+ Subgroup Analysis in Clinical Trials 2017 Alex Dmitrienko
Gautier Paux
+ A comparative study of subgroup identification methods for differential treatment effect: Performance metrics and recommendations 2017 Demissie Alemayehu
Yang Chen
Marianthi Markatou
+ Comparing Approaches to Treatment Effect Estimation for Subgroups in Clinical Trials 2016 Marius Thomas
Björn Bornkamp
+ Comparing Approaches to Treatment Effect Estimation for Subgroups in Clinical Trials 2016 Marius Thomas
Björn Bornkamp
+ Subgroup Identification for Tailored Therapies: Methods and Consistent Evaluation 2020 Lei Shen
Hollins Showalter
Chakib Battioui
Brian T. Denton
+ PDF Chat Robustness of testing procedures for confirmatory subpopulation analyses based on a continuous biomarker 2018 Alexandra Gráf
Gernot Wassmer
Tim Friede
Roland G. Gera
Martin Posch

Works That Cite This (19)

Action Title Year Authors
+ PDF Chat Adaptive enrichment trial designs using joint modelling of longitudinal and time-to-event data 2024 Abigail Burdon
Richard D. Baird
Thomas Jaki
+ Point estimation for adaptive trial designs 2021 David S. Robertson
Babak Choodari‐Oskooei
Munyaradzi Dimairo
Laura Flight
Philip Pallmann
Thomas Jaki
+ PDF Chat The Adaptive designs CONSORT Extension (ACE) statement: a checklist with explanation and elaboration guideline for reporting randomised trials that use an adaptive design 2020 Munyaradzi Dimairo
Philip Pallmann
James Wason
Susan Todd
Thomas Jaki
Steven A. Julious
Adrian Mander
Christopher J. Weir
Franz Koenig
Marc K. Walton
+ PDF Chat The Adaptive designs CONSORT Extension (ACE) Statement: A checklist with explanation and elaboration guideline for reporting randomised trials that use an adaptive design 2019 Munyaradzi Dimairo
Philip Pallmann
James Wason
Susan Todd
Thomas Jaki
Steven A. Julious
Adrian Mander
Christopher J. Weir
Franz Koenig
Marc K. Walton
+ PDF Chat The adaptive designs CONSORT extension (ACE) statement: a checklist with explanation and elaboration guideline for reporting randomised trials that use an adaptive design 2020 Munyaradzi Dimairo
Philip Pallmann
James Wason
Susan Todd
Thomas Jaki
Steven A. Julious
Adrian Mander
Christopher J. Weir
Franz Koenig
Marc K. Walton
+ A conditional error function approach for adaptive enrichment designs with continuous endpoints 2019 Marius Placzek
Tim Friede
+ PDF Chat On estimating the selected treatment mean under a two‐stage adaptive design 2023 Masihuddin
Neeraj Misra
+ PDF Chat Point and interval estimation in two‐stage adaptive designs with time to event data and biomarker‐driven subpopulation selection 2020 Peter Kimani
Susan Todd
Lindsay A. Renfro
Ekkehard Glimm
Jamal Nasir Khan
John A. Kairalla
Nigel Stallard
+ Efficient adaptive designs for clinical trials of interventions for COVID-19 2020 Nigel Stallard
Lisa V. Hampson
Norbert Benda
Werner Brannath
Tom Burnett
Tim Friede
Peter Kimani
Franz Koenig
Johannes Krisam
Pavel Mozgunov
+ PDF Chat Point estimation for adaptive trial designs I: A methodological review 2022 David S. Robertson
Babak Choodari‐Oskooei
Munyaradzi Dimairo
Laura Flight
Philip Pallmann
Thomas Jaki