Evidence map›Paper›PMID 31631254›Full record

ArticlePharmacoEconomics2020

Influence of Modeling Choices on Value of Information Analysis: An Empirical Analysis from a Real-World Experiment.

David D Kim, Gregory F Guzauskas, Caroline S Bennette, Anirban Basu, David L Veenstra, Scott D Ramsey, Josh J Carlson

Abstract read
PubMed Publisher
In one paragraph

Article in PharmacoEconomics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.5field-weighted citation impact, top 18% of its field
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

0 citing papers in PubMed, 3 citations in OpenAlex.

No citing paper in PubMed yet.

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 at 4 institutions in 1 country.

David D KimCenter for the Evaluation of Value and Risk in Health, Institute for Clinical Research and Health Policy Studies, Tufts Medical Center, 800 Washington St., Box 63, Boston, MA, 02111, USA. dkim3@tuftsmedicalcenter.org.ORCID 0000-0002-3383-8972
Gregory F GuzauskasDepartment of Pharmacy, University of Washington, Seattle, WA, USA.
Caroline S BennetteFlatiron Health, New York, NY, USA.
Anirban BasuDepartment of Pharmacy, University of Washington, Seattle, WA, USA.
David L VeenstraDepartment of Pharmacy, University of Washington, Seattle, WA, USA.
Scott D RamseyHutchinson Institute for Cancer Outcomes Research, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
Josh J CarlsonDepartment of Pharmacy, University of Washington, Seattle, WA, USA.
University of Washington · USFlatiron Health (United States) · USFred Hutch Cancer Center · USTufts Medical Center · US

Funding

SWOG NCORP Research BaseUG1CA189974 · NCI · THE HOPE FOUNDATION · PI CHARLES D. BLANKE, DAWN HERSHMAN · 2014 to 2026
$80.6M
NCI NIH HHS UG1 CA189974Patient-Centered Outcomes Research Institute ME-1303-5889
6 · The paper itself

Abstract

backgroundValue of information (VOI) analysis often requires modeling to characterize and propagate uncertainty. In collaboration with a cancer clinical trial group, we integrated a VOI approach to assessing trial proposals.

objectiveThis paper aims to explore the impact of modeling choices on VOI results and to share lessons learned from the experience.

methodsAfter selecting two proposals (A: phase III, breast cancer; B: phase II, pancreatic cancer) for in-depth evaluations, we categorized key modeling choices relevant to trial decision makers (characterizing uncertainty of efficacy, evidence thresholds to change clinical practice, and sample size) and modelers (cycle length, survival distribution, simulation runs, and other choices). Using a $150,000 per quality-adjusted life-year (QALY) threshold, we calculated the patient-level expected value of sample information (EVSI) for each proposal and examined whether each modeling choice led to relative change of more than 10% from the averaged base-case estimate. We separately analyzed the impact of the effective time horizon.

resultsThe base-case EVSI was $118,300 for Proposal A and $22,200 for Proposal B per patient. Characterizing uncertainty of efficacy was the most important choice in both proposals (e.g. Proposal A: $118,300 using historical data vs. $348,300 using expert survey), followed by the sample size and the choice of survival distribution. The assumed effective time horizon also had a substantial impact on the population-level EVSI.

conclusionsModeling choices can have a substantial impact on VOI. Therefore, it is important for groups working to incorporate VOI into research prioritization to adhere to best practices, be clear in their reporting and justification for modeling choices, and to work closely with the relevant decision makers, with particular attention to modeling choices.

Indexed as

Models, EconomicBreast NeoplasmsClinical Trials, Phase II as TopicClinical Trials, Phase III as TopicCost-Benefit AnalysisFemaleHumansPancreatic NeoplasmsQuality-Adjusted Life YearsResearch DesignTechnology Assessment, BiomedicalUncertainty

Identifiers

PMID31631254
OpenAlexW2981299873

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.