Within trial comparison of survival time projections from short-term follow-up with long-term follow-up findings.

Long-term follow-up Randomized controlled trials Restricted mean survival time Survival estimates

Journal

ESC heart failure
ISSN: 2055-5822
Titre abrégé: ESC Heart Fail
Pays: England
ID NLM: 101669191

Informations de publication

Date de publication:
10 2022
Historique:
revised: 04 10 2021
received: 14 06 2021
accepted: 11 11 2021
pubmed: 9 7 2022
medline: 6 12 2022
entrez: 8 7 2022
Statut: ppublish

Résumé

Data on long-term treatment effects are scarce, despite the intent to use new therapies for many years and the need of patients, physicians and payers to have a better understanding of the lifetime benefits of treatments. The restricted mean or median survival time (RMST) calculated using age instead of time, hypothetically enables estimation of long-term gain in event-free or overall survival from the short-term (within-trial) effects of an intervention, compared with its control. Tha aim of the study is to use trials with long-term follow-up available through extension studies to compare the long-term projections estimated using RMST from within-trial follow-up data with the actual long-term outcomes in the extension studies. We estimated the median long-term survival time using age instead of follow-up time and compared these model-based projections with the actual long-term estimates in the (i) SCD-HeFT trial vs. SCD-HeFT long-term outcomes; (ii) SOLVD trial vs. SOLVD 12 year follow-up; (iii) STICH trial vs. STICHES; and (iv) ACCORD study vs. ACCORDION. In the long-term follow-up of SCD-HeFT, gain in survival with ICD vs. placebo over a median of 11.0 years was +1.4 years of life. The RMST model-derived survival projection from the within-trial data (median follow-up of 3.4 years) gave an estimated survival gain of +1.2 years. In STICHES, over a median follow-up of 9.8 years, coronary artery bypass grafting (CABG) vs. medical care led to a survival extension of +1.4 years in favour of CABG. RMST projections using within-trial data from STICH (median follow-up of 4.9 years), gave an extended survival of +2.4 years in favour of CABG in younger patients. In the long-term follow-up of SOLVD, enalapril vs. placebo led to a survival gain of +0.8 years over a median follow-up of 12.1 years. The RMST projections from the within-trial data (median follow-up of 2.8 years) gave a survival extension of +0.3 years in favour of enalapril. In the long-term follow-up ACCORDION study, with a median follow-up of 8.8 years, intensive vs. a standard anti-hyperglycaemic treatment did not influence long-term survival, which was concordant with the RMST projections from the short-term ACCORD study with median follow-up of 4.9 years. Age-based survival projections using within-trial data generally provided concordant results with the actual survival measured in long-term follow-up extension studies. Our findings suggest that age-based lifetime projections may be used as means to assess the long-term treatment effects.

Identifiants

pubmed: 35799450
doi: 10.1002/ehf2.13731
pmc: PMC9715817
doi:

Substances chimiques

Enalapril 69PN84IO1A

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

3655-3658

Subventions

Organisme : British Heart Foundation
ID : RE/18/6/34217
Pays : United Kingdom

Informations de copyright

© 2021 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology.

Références

J Am Coll Cardiol. 2018 Jun 12;71(23):2640-2642
pubmed: 29880123
ESC Heart Fail. 2022 Oct;9(5):3655-3658
pubmed: 35799450
N Engl J Med. 2015 Dec 3;373(23):2289-90
pubmed: 26630151
Stat Med. 2008 Nov 20;27(26):5525-55
pubmed: 18613251
J Clin Oncol. 2014 Aug 1;32(22):2380-5
pubmed: 24982461
JACC Heart Fail. 2020 Dec;8(12):984-995
pubmed: 33039448
Circulation. 2018 Oct 9;138(15):1599-1601
pubmed: 30354516
Circulation. 2016 Nov 1;134(18):1314-1324
pubmed: 27573034

Auteurs

João Pedro Ferreira (JP)

INSERM, Centre d'Investigations Cliniques-1433, INI CRCT, INSERM U1116, CHRU Nancy, Université de Lorraine, Nancy, France.
British Heart Foundation Cardiovascular Research Centre, University of Glasgow, 126 University Place, Glasgow, G12 8TA, UK.

Brian L Claggett (BL)

Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

Kieran F Docherty (KF)

British Heart Foundation Cardiovascular Research Centre, University of Glasgow, 126 University Place, Glasgow, G12 8TA, UK.

Pardeep S Jhund (PS)

British Heart Foundation Cardiovascular Research Centre, University of Glasgow, 126 University Place, Glasgow, G12 8TA, UK.

Faiez Zannad (F)

INSERM, Centre d'Investigations Cliniques-1433, INI CRCT, INSERM U1116, CHRU Nancy, Université de Lorraine, Nancy, France.

Scott D Solomon (SD)

Cardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

John J V McMurray (JJV)

British Heart Foundation Cardiovascular Research Centre, University of Glasgow, 126 University Place, Glasgow, G12 8TA, UK.

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