Extrapolating Survival Data Using Historical Trial-Based a Priori Distributions.


Journal

Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research
ISSN: 1524-4733
Titre abrégé: Value Health
Pays: United States
ID NLM: 100883818

Informations de publication

Date de publication:
09 2019
Historique:
received: 16 02 2018
revised: 28 02 2019
accepted: 22 03 2019
entrez: 13 9 2019
pubmed: 13 9 2019
medline: 14 4 2020
Statut: ppublish

Résumé

To show how clinical trial data can be extrapolated using historical trial data-based a priori distributions. Extrapolations based on 30-month pivotal multiple myeloma trial data were compared with 75-month data from the same trial. The 30-month data represent a typical decision-making scenario where early results from a clinical trial are extrapolated. Mature historical trial data with the same comparator as in the pivotal trial were incorporated in 2 stages. First, the parametric distribution selection was based on the historical trial data. Second, the shape parameter estimate of the historical trial was used to define an informative a priori distribution for the shape of the 30-month pivotal trial data. The method was compared with standard approaches, fitting parametric distributions to the 30-month data with noninformative prior. The predicted survival of each method was compared with the observed survival (ΔAUC) in the 75-month trial data. The Weibull had the best fit to the historical trial and the log-normal to the 30-month pivotal trial data. The ΔAUC of the Weibull with informative priors was considerably smaller compared with the standard Weibull. Also, the predicted median survival based on the Weibull with informative priors was more accurate (melphalan and prednisone [MP] 40 months, and bortezomib [V] combined with MP [VMP] 62 months) than based on the standard Weibull (MP 45 months and VMP 72 months) when compared with the observed median (MP 41.3 months and VMP 56.4 months). Extrapolation of clinical trial data is improved by using historical trial data-based informative a priori distributions.

Identifiants

pubmed: 31511177
pii: S1098-3015(19)32125-4
doi: 10.1016/j.jval.2019.03.017
pii:
doi:

Substances chimiques

Antineoplastic Agents 0
Bortezomib 69G8BD63PP
Melphalan Q41OR9510P
Prednisone VB0R961HZT

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1012-1017

Informations de copyright

Copyright © 2019 ISPOR–The Professional Society for Health Economics and Outcomes Research. Published by Elsevier Inc. All rights reserved.

Auteurs

Fanni Soikkeli (F)

Ingress Health, Rotterdam, The Netherlands. Electronic address: fanni.soikkeli@ingress-health.com.

Mahmoud Hashim (M)

Ingress Health, Rotterdam, The Netherlands.

Mario Ouwens (M)

AstraZeneca R&D, Mölndal, Sweden.

Maarten Postma (M)

Department of Health Sciences, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.

Bart Heeg (B)

Ingress Health, Rotterdam, The Netherlands.

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Classifications MeSH