Evidence map›Paper›PMID 30224106›Full record

ReviewValue in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research2018

Methodological Issues in Assessing the Economic Value of Next-Generation Sequencing Tests: Many Challenges and Not Enough Solutions.

Kathryn A Phillips, Patricia A Deverka, Deborah A Marshall, Sarah Wordsworth, Dean A Regier, Kurt D Christensen, James Buchanan

Erratum issuedAbstract readReview
In one paragraph

Review in Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 43 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 5 pooled it
–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

43 citing papers in PubMed, 5 syntheses or guidelines pooled it.

  1. Pooled it
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  6. Quantifying Downstream Healthcare Utilization in Studies of Genomic Testing.Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research · 2020
    Trial
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  8. Is next generation sequencing for the diagnosis of rare diseases worth its cost? A user-based approach to valuation.The European journal of health economics : HEPAC : health economics in prevention and care · 2026
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Kathryn A PhillipsDepartment of Clinical Pharmacy; Center for Translational and Policy Research on Personalized Medicine (TRANSPERS); UCSF Philip R. Lee Institute for Health Policy; and UCSF Helen Diller Family Comprehensive Cancer Center, University of California San Francisco, San Francisco, CA, USA. Electronic address: kathryn.Phillips@ucsf.edu.
Patricia A DeverkaAmerican Institutes for Research, Chapel Hill, NC, USA.
Deborah A MarshallDepartment of Community Health Sciences, University of Calgary, Calgary, Alberta, Canada.
Sarah WordsworthNuffield Department of Population Health, Medical Sciences Division, University of Oxford, Oxford, UK.
Dean A RegierCancer Control BC, School of Population and Public Health, University of British Columbia, Vancouver, British Columbia, Canada.
Kurt D ChristensenBrigham and Women's Hospital, Harvard University, Boston, MA, USA.
James BuchananNuffield Department of Population Health, Medical Sciences Division, University of Oxford, Oxford, UK.

Funding

Risk-Benefit Trade-Offs for Whole Genome SequencingR01HG007063 · NHGRI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI PHILLIPS, KATHRYN A · 2013 to 2016
$2.5M
NHGRI NIH HHS R01 HG007063
6 · The paper itself

Abstract

backgroundClinical use of next-generation sequencing (NGS) tests has been increasing, but few studies have examined their economic value. Several studies have noted that there are methodological challenges to conducting economic evaluations of NGS tests.

objectiveOur objective was to examine key methodological challenges for conducting economic evaluations of NGS tests, prioritize these challenges for future research, and identify how studies have attempted solutions to address these challenges.

methodsWe identified challenges for economic evaluations of NGS tests using prior literature and expert judgment of the co-authors. We used a modified Delphi assessment to prioritize challenges, based on importance and probability of resolution. Using a structured literature review and article extraction we then assessed whether published economic evaluations had addressed these challenges.

resultsWe identified 11 challenges for conducting economic evaluations of NGS tests. The experts identified three challenges as the top priorities for future research: complex model structure, timeframe, and type of analysis and comparators used. Of the 15 published studies included in our literature review, four studies described specific solutions relevant to five of the 11 identified challenges.

conclusionsMajor methodological challenges to economic evaluations of NGS tests remain to be addressed. Our results can be used to guide future research and inform decision-makers on how to prioritize research on the economic assessment of NGS tests.

Indexed as

Cost-Benefit AnalysisDelphi TechniqueHigh-Throughput Nucleotide SequencingHumansTechnology Assessment, Biomedicaleconomicsmethods developmentnext-generation sequencingpersonalized medicineprecision medicine

Identifiers

PMID30224106
PMCPMC6159915

What OpenQuestion holds

Textmetadata
LicenceTDM
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.