Reweighting Randomized Controlled Trial Evidence to Better Reflect Real Life - A Case Study of the Innovative Medicines Initiative.


Journal

Clinical pharmacology and therapeutics
ISSN: 1532-6535
Titre abrégé: Clin Pharmacol Ther
Pays: United States
ID NLM: 0372741

Informations de publication

Date de publication:
10 2020
Historique:
received: 05 11 2019
accepted: 31 03 2020
pubmed: 18 4 2020
medline: 25 5 2021
entrez: 18 4 2020
Statut: ppublish

Résumé

Evidence from randomized controlled trials available for timely health technology assessments of new pharmacological treatments and regulatory decision making may not be generalizable to local patient populations, often resulting in decisions being made under uncertainty. In recent years, several reweighting approaches have been explored to address this important question of generalizability to a target population. We present a case study of the Innovative Medicines Initiative to illustrate the inverse propensity score reweighting methodology, which may allow us to estimate the expected treatment benefit if a clinical trial had been run in a broader real-world target population. We learned that identifying treatment effect modifiers, understanding and managing differences between patient characteristic data sets, and balancing the closeness of trial and target patient populations with effective sample size are key to successfully using this methodology and potentially mitigating some of this uncertainty around local decision making.

Identifiants

pubmed: 32301116
doi: 10.1002/cpt.1854
pmc: PMC7540324
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

817-825

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2020 The Authors. Clinical Pharmacology & Therapeutics published by Wiley Periodicals LLC on behalf of American Society for Clinical Pharmacology and Therapeutics.

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Auteurs

Michael Happich (M)

Lilly Research Centre, Eli Lilly and Company, Surrey, UK.

Alan Brnabic (A)

Eli Lilly and Company, Sydney, New South Wales, Australia.

Douglas Faries (D)

Lilly Corporate Center, Eli Lilly and Company, Indianapolis, Indiana, USA.

Keith Abrams (K)

Department of Health Sciences, University of Leicester, Leicester, UK.

Katherine B Winfree (KB)

Lilly Corporate Center, Eli Lilly and Company, Indianapolis, Indiana, USA.

Allicia Girvan (A)

Lilly Corporate Center, Eli Lilly and Company, Indianapolis, Indiana, USA.

Pall Jonsson (P)

National Institute for Health and Care Excellence (NICE), Manchester, UK.

Joseph Johnston (J)

Lilly Corporate Center, Eli Lilly and Company, Indianapolis, Indiana, USA.

Mark Belger (M)

Lilly Research Centre, Eli Lilly and Company, Surrey, UK.

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Classifications MeSH