Cost-effectiveness of a new autoantibody test added to Computed Tomography (CT) compared to CT surveillance alone in the diagnosis of lung cancer amongst patients with indeterminate pulmonary nodules.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2020
Historique:
received: 24 05 2019
accepted: 28 07 2020
entrez: 3 9 2020
pubmed: 3 9 2020
medline: 21 10 2020
Statut: epublish

Résumé

Oncimmune's EarlyCDT®-Lung is a simple ELISA blood test that measures seven lung cancer specific autoantibodies and is used in the assessment of malignancy risk in patients with indeterminate pulmonary nodules (IPNs). The objective of this study was to examine the cost-effectiveness of EarlyCDT-Lung in the diagnosis of lung cancer amongst patients with IPNs in addition to CT surveillance, compared to CT surveillance alone which is the current recommendation by the British Thoracic Society guidelines. A model consisting of a combination of a decision tree and Markov model was developed using the outcome measure of the quality adjusted life year (QALY). A life-time time horizon was adopted. The model was parameterized using a range of secondary sources. At £70 per test, EarlyCDT-Lung and CT surveillance was found to be cost-effective compared to CT surveillance alone with an incremental cost-effectiveness ratio (ICER) of less than £2,500 depending on the test accuracy parameters used. It was also found that EarlyCDT-Lung can be priced up to £1,177 and still be cost-effective based on cost-effectiveness acceptance threshold of £20,000 / QALY. Further research to resolve parameter uncertainty, was not found to be of value. The results here demonstrate that at £70 per test the EarlyCDT-Lung will have a positive impact on patient outcomes and coupled with CT surveillance is a cost-effective approach to the management of patients with IPNs. The conclusions drawn from this analysis are robust to realistic variation in the parameters used in the model.

Identifiants

pubmed: 32877432
doi: 10.1371/journal.pone.0237492
pii: PONE-D-19-14772
pmc: PMC7467291
doi:

Substances chimiques

Autoantibodies 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0237492

Déclaration de conflit d'intérêts

I have read the journal's policy and the authors of this manuscript have the following competing interests: LJ, MF, GHF, AM, and AH are full-time employees of Oncimmune Limited. This does not alter our adherence to PLOS ONE policies on sharing data and materials.

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Auteurs

Andrew John Sutton (AJ)

Institute of Health Economics, Edmonton, Alberta, Canada.

Gurdeep S Sagoo (GS)

Test Evaluation Group, Institute of Health Sciences, University of Leeds, Leeds, United Kingdom.

Leon Jackson (L)

Oncimmune Limited, City Hospital, Clinical Sciences Building, Nottingham, United Kingdom.

Mike Fisher (M)

Oncimmune Limited, City Hospital, Clinical Sciences Building, Nottingham, United Kingdom.

Geoffrey Hamilton-Fairley (G)

Oncimmune Limited, City Hospital, Clinical Sciences Building, Nottingham, United Kingdom.

Andrea Murray (A)

Oncimmune Limited, City Hospital, Clinical Sciences Building, Nottingham, United Kingdom.

Adam Hill (A)

Oncimmune Limited, City Hospital, Clinical Sciences Building, Nottingham, United Kingdom.
Institute of Global Health Innovation, Imperial College London, South Kensington Campus, London, United Kingdom.

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Classifications MeSH