Evidence map›Paper›PMID 36826141›Full record

ArticleCurrent oncology (Toronto, Ont.)2023

Cost Savings of Expedited Care with Upfront Next-Generation Sequencing Testing versus Single-Gene Testing among Patients with Metastatic Non-Small Cell Lung Cancer Based on Current Canadian Practices.

Brandon S Sheffield, Kiefer Eaton, Bruno Emond, Marie-Hélène Lafeuille, Annalise Hilts, Patrick Lefebvre, Laura Morrison, Andrea L Stevens, Emmanuel M Ewara, Parneet Cheema

Open access · goldAbstract read
In one paragraph

Article in Current oncology (Toronto, Ont.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
7.9field-weighted citation impact, top 2% 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

27 citing papers in PubMed, 33 citations in OpenAlex.

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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

10 authors at 3 institutions in 2 countries.

Brandon S SheffieldWilliam Osler Health System, Brampton, ON L6R 3J7, Canada.
Kiefer EatonJanssen, Inc., Toronto, ON M3C 1L9, Canada.ORCID 0000-0002-4369-233X
Bruno EmondAnalysis Group, Inc., Montréal, QC H3B 0G7, Canada.ORCID 0000-0002-0060-765X
Marie-Hélène LafeuilleAnalysis Group, Inc., Montréal, QC H3B 0G7, Canada.
Annalise HiltsAnalysis Group, Inc., Montréal, QC H3B 0G7, Canada.
Patrick LefebvreAnalysis Group, Inc., Montréal, QC H3B 0G7, Canada.
Laura MorrisonAnalysis Group, Inc., Montréal, QC H3B 0G7, Canada.
Andrea L StevensJanssen Global Services, Inc., Raritan, NJ 08869, USA.ORCID 0000-0002-2892-7065
Emmanuel M EwaraJanssen, Inc., Toronto, ON M3C 1L9, Canada.
Parneet CheemaWilliam Osler Health System, Brampton, ON L6R 3J7, Canada.
Group for Research in Decision Analysis · CAWilliam Osler Health System · CAJanssen (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study assessed the total costs of testing, including the estimated costs of delaying care, associated with next-generation sequencing (NGS) versus single-gene testing strategies among patients with newly diagnosed metastatic non-small cell lung cancer (mNSCLC) from a Canadian public payer perspective. A decision tree model considered testing for genomic alterations using tissue biopsy NGS or single-gene strategies following Canadian guideline recommendations. Inputs included prevalence of mNSCLC, the proportion that tested positive for each genomic alteration, rebiopsy rates, time to test results, testing/medical costs, and costs of delaying care based on literature, public data, and expert opinion. Among 1,000,000 hypothetical publicly insured adult Canadians (382 with mNSCLC), the proportion of patients that tested positive for a genomic alteration with an approved targeted therapy was 38.0% for NGS and 26.1% for single-gene strategies. The estimated mean time to appropriate targeted therapy initiation was 5.1 weeks for NGS and 9.2 weeks for single-gene strategies. Based on literature, each week of delayed care cost CAD 406, translating to total mean per-patient costs of CAD 3480 for NGS and CAD 5632 for single-gene strategies. NGS testing with mNSCLC in current Canadian practice resulted in more patients with an identified mutation, shorter time to appropriate targeted therapy initiation, and lower total testing costs compared to single-gene strategies.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsAdultCanadaCost SavingsHigh-Throughput Nucleotide SequencingHumanseconomic modelmedical costsnext-generation sequencingnon-small cell lung cancertesting costs

Identifiers

PMID36826141
PMCPMC9955559
OpenAlexW4321105941

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.