Evidence map›Paper›PMID 34405371›Full record

SynthesisPharmacoEconomics2021

Early Cost Effectiveness of Whole-Genome Sequencing as a Clinical Diagnostic Test for Patients with Inoperable Stage IIIB,C/IV Non-squamous Non-small-Cell Lung Cancer.

Martijn J H G Simons, Valesca P Retèl, Bram L T Ramaekers, Rogier Butter, Joanne M Mankor, Marthe S Paats, Joachim G J V Aerts, Zakile A Mfumbilwa, Paul Roepman, Veerle M H Coupé and 3 more

Open access · hybridAbstract readSystematic Review
In one paragraph

Synthesis in PharmacoEconomics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 3 pooled it
2.8field-weighted citation impact, top 8% 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

21 citing papers in PubMed, 3 syntheses or guidelines pooled it, 34 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Article
  5. Article
  6. Article
  7. Observational
  8. Article
  9. Article
  10. How is Value Defined in Molecular Testing in Cancer? A Scoping Review.Applied health economics and health policy · 2025
    Article
  11. Article
  12. Article
  13. Cholangiocarcinoma: The era of liquid biopsy.World journal of gastroenterology · 2025
    Review
  14. Observational
  15. Review
  16. Article
  17. Article
  18. Article
  19. Resource allocation in genetic and genomic medicine.Journal of community genetics · 2022
    Article
  20. 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

13 authors at 6 institutions in 2 countries.

Martijn J H G SimonsDepartment of Clinical Epidemiology and Medical Technology Assessment, Maastricht University Medical Centre, P. Debyelaan 25, P.O. Box 5800, 6202 AZ, Maastricht, The Netherlands.ORCID 0000-0001-5248-1676
Valesca P RetèlDepartment of Psychosocial Research and Epidemiology, Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital, Plesmanlaan 121, 1066 CX, Amsterdam, The Netherlands.ORCID 0000-0002-5624-3234
Bram L T RamaekersDepartment of Clinical Epidemiology and Medical Technology Assessment, Maastricht University Medical Centre, P. Debyelaan 25, P.O. Box 5800, 6202 AZ, Maastricht, The Netherlands.ORCID 0000-0001-5785-9228
Rogier ButterDepartment of Pathology, Cancer Center Amsterdam, Amsterdam University Medical Center, University of Amsterdam, Meibergdreef 9, 1105 AZ, Amsterdam, The Netherlands.ORCID 0000-0002-4277-6814
Joanne M MankorDepartment of Pulmonary Medicine, Erasmus Medical Centre, Doctor Molewaterplein 40, 3015 GD, Rotterdam, The Netherlands.ORCID 0000-0003-3653-9043
Marthe S PaatsDepartment of Pulmonary Medicine, Erasmus Medical Centre, Doctor Molewaterplein 40, 3015 GD, Rotterdam, The Netherlands.
Joachim G J V AertsDepartment of Pulmonary Medicine, Erasmus Medical Centre, Doctor Molewaterplein 40, 3015 GD, Rotterdam, The Netherlands.ORCID 0000-0001-6662-2951
Zakile A MfumbilwaDepartment of Epidemiology and Data Science, Amsterdam University Medical Center-Location VUmc, Van der Boechorststraat 7, 1081 BT, Amsterdam, The Netherlands.ORCID 0000-0002-9705-7227
Paul RoepmanHartwig Medical Foundation, Science Park 408, 1098 XH, Amsterdam, The Netherlands.ORCID 0000-0003-1566-0258
Veerle M H CoupéDepartment of Epidemiology and Data Science, Amsterdam University Medical Center-Location VUmc, Van der Boechorststraat 7, 1081 BT, Amsterdam, The Netherlands.ORCID 0000-0002-9553-9791
Carin A Uyl-de GrootErasmus School of Health Policy and Management/Institute for Medical Technology Assessment, Erasmus University Rotterdam, Burgemeester Oudlaan 50, 3062 PA, Rotterdam, The Netherlands.ORCID 0000-0001-6492-5203
Wim H van HartenDepartment of Psychosocial Research and Epidemiology, Netherlands Cancer Institute-Antoni van Leeuwenhoek Hospital, Plesmanlaan 121, 1066 CX, Amsterdam, The Netherlands.ORCID 0000-0001-9580-0489
Manuela A JooreDepartment of Clinical Epidemiology and Medical Technology Assessment, Maastricht University Medical Centre, P. Debyelaan 25, P.O. Box 5800, 6202 AZ, Maastricht, The Netherlands. m.joore@mumc.nl.ORCID 0000-0002-5649-6768
Erasmus University Rotterdam · NLMaastricht University Medical Centre · NLAmsterdam University Medical Centers · NLThe Netherlands Cancer Institute · NLHartwig Medical Foundation · NLUniversity Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAdvanced non-small-cell lung cancer (NSCLC) harbours many genetic aberrations that can be targeted with systemic treatments. Whole-genome sequencing (WGS) can simultaneously detect these (and possibly new) molecular targets. However, the exact added clinical value of WGS is unknown.

objectiveThe objective of this study was to determine the early cost effectiveness of using WGS in diagnostic strategies compared with currently used molecular diagnostics for patients with inoperable stage IIIB,C/IV non-squamous NSCLC from a Dutch healthcare perspective.

methodsA decision tree represented the diagnostic pathway, and a cohort state transition model represented disease progression. Three diagnostic strategies were modelled: standard of care (SoC) alone, WGS as a diagnostic test, and SoC followed by WGS. Treatment effectiveness was based on a systematic review. Probabilistic cost-effectiveness analyses were performed, and threshold analyses (using €80,000 per quality-adjusted life-year [QALY]) was used to explore the early cost effectiveness of WGS.

resultsWGS as a diagnostic test resulted in more QALYs (0.002) and costs (€1534 [incremental net monetary benefit -€1349]), and SoC followed by WGS resulted in fewer QALYs (-0.002) and more costs (€1059 [-€1194]) compared with SoC alone. WGS as a diagnostic test was only cost effective if it was priced at €2000 per patient and identified 2.7% more actionable patients than SoC alone. Treating these additional identified patients with new treatments costing >€4069 per month decreased the probability of cost effectiveness.

conclusionsOur analysis suggests that providing WGS as a diagnostic test is cost effective compared with SoC followed by WGS and SoC alone if costs for WGS decrease and additional patients with actionable targets are identified. This cost-effectiveness model can be used to incorporate new findings iteratively and to support ongoing decision making regarding the use of WGS in this rapidly evolving field.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsCost-Benefit AnalysisDiagnostic Tests, RoutineHumansQuality-Adjusted Life Years

Identifiers

PMID34405371
PMCPMC8599348
OpenAlexW3195223644

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.