Evidence map›Paper›PMID 40927977›Full record

ArticleJournal of comparative effectiveness research2025

Composite endpoints in health technology assessment: Part 1 - an illustration of best modeling practice.

Andrew Briggs, Aris Angelis, Jieling Chen, David Booth, Jason A Davis, Muthiah Vaduganathan, Pardeep S Jhund

Abstract read
In one paragraph

Article in Journal of comparative effectiveness research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Andrew BriggsDepartment of Health Services Research & Policy, London School of Hygiene & Tropical Medicine, London, UK.ORCID 0000-0002-0777-1997
Aris AngelisDepartment of Health Services Research & Policy, London School of Hygiene & Tropical Medicine, London, UK.ORCID 0000-0002-0261-4634
Jieling ChenGlobal Market Access & Pricing, AstraZeneca R&D, Gaithersburg, MD 20878, USA.
David BoothHealth Economics & Outcomes Research Ltd, Cardiff, UK.
Jason A DavisHealth Economics & Outcomes Research Ltd, Cardiff, UK.
Muthiah VaduganathanCardiovascular Division & Center for Cardiometabolic Implementation Science, Brigham & Women's Hospital, Harvard Medical School, Boston, MA 02115, USA.
Pardeep S JhundBritish Heart Foundation, University of Glasgow, Glasgow, UK.ORCID 0000-0003-4306-5317

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Composite endpoints amalgamate multiple clinical outcomes into a single measure, offering efficiency gains in clinical trials through increased event rates and reduced sample sizes, thus accelerating clinical development and regulatory approval. However, employing composite endpoints introduces complexities into health technology assessments (HTAs), particularly in economic modeling, due to the varying clinical significance and cost implications of the components. In this paper, we explore best modeling practice for HTAs that are based on clinical trials that employ composite endpoints. We examine regulatory guidance and discuss statistical solutions for differential component impacts, before presenting a case study based on a recent dapagliflozin submission for reimbursement in heart failure. Our investigation reveals that while composite endpoints can streamline trial analyses and hasten regulatory approval, they also pose a risk of bias in HTA if treatment effects for the components are inappropriately pooled. The paper discusses HTA principles in the context of composite endpoint trials and proposes strategies to develop modeling scenarios and interpret results, especially concerning whether to combine or split out estimates of component treatment effects. A particular focus is the accurate capture of uncertainty, both in terms of the parameter inputs to the model and over the ultimate decision to reimburse. This paper serves as a potential resource for researchers, practitioners and decision-makers, offering insights into best modeling practices that can unlock the full potential of composite endpoints in the pursuit of evidence-based healthcare decision-making.

Indexed as

Endpoint DeterminationModels, EconomicTechnology Assessment, BiomedicalBenzhydryl CompoundsClinical Trials as TopicGlucosidesHeart FailureHumansUncertaintyBenzhydryl CompoundsdapagliflozinGlucosidescase studycomposite endpointscost-effectivenesshealth economic modelinghealth technology assessmentuncertainty

Identifiers

PMID40927977
PMCPMC12465925

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.