Evidence map›Paper›PMID 33786799›Full record

ArticlePharmacoEconomics2021

Cost-Effectiveness Analysis of Afatinib, Erlotinib, and Gefitinib as First-Line Treatments for EGFR Mutation-Positive Non-Small-Cell Lung Cancer in Ontario, Canada.

Yong-Jin Kim, Mark Oremus, Helen H Chen, Thomas McFarlane, Danielle Fearon, Susan Horton

Abstract read
PubMed Publisher
In one paragraph

Article in PharmacoEconomics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

1 citing paper in PubMed, 8 citations in OpenAlex.

  1. Receptor tyrosine kinase inhibitors in cancer.Cellular and molecular life sciences : CMLS · 2023
    Review
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

6 authors at 1 institution in 1 country.

Yong-Jin KimSchool of Public Health and Health Systems, University of Waterloo, Lyle Hallman North Building-2714, 200 University Ave W, Waterloo, ON, N2L 3G1, Canada. y238kim@uwaterloo.ca.ORCID http://orcid.org/0000-0002-3055-9943
Mark OremusSchool of Public Health and Health Systems, University of Waterloo, Lyle Hallman North Building-2714, 200 University Ave W, Waterloo, ON, N2L 3G1, Canada.ORCID http://orcid.org/0000-0001-8190-253X
Helen H ChenSchool of Public Health and Health Systems, University of Waterloo, Lyle Hallman North Building-2714, 200 University Ave W, Waterloo, ON, N2L 3G1, Canada.ORCID http://orcid.org/0000-0002-9401-7895
Thomas McFarlaneSchool of Pharmacy, University of Waterloo, Kitchener, ON, Canada.ORCID http://orcid.org/0000-0003-0871-8773
Danielle FearonSchool of Public Health and Health Systems, University of Waterloo, Lyle Hallman North Building-2714, 200 University Ave W, Waterloo, ON, N2L 3G1, Canada.
Susan HortonSchool of Public Health and Health Systems, University of Waterloo, Lyle Hallman North Building-2714, 200 University Ave W, Waterloo, ON, N2L 3G1, Canada.ORCID http://orcid.org/0000-0002-9243-4767
University of Waterloo · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe objective of this study was to compare the cost effectiveness of first-line epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) for the treatment of non-small-cell lung cancer.

methodsThis study used Ontario Cancer Registry-linked administrative data to identify patients with a primary diagnosis of lung cancer who received EGFR-TKIs as first-line treatment between 1 January, 2014 and 31 August, 2019. A net benefit regression approach accounting for baseline covariates and propensity scores was used to estimate incremental net benefits and incremental cost-effectiveness ratios. Outcome measures were calculated over a 68-month period and were discounted with an annual rate of 1.5%. Sensitivity analyses were conducted to assess and characterize the uncertainties.

resultsA total of 547 patients were included in the study, of whom 20.1%, 23.6%, and 56.3% received afatinib, erlotinib, and gefitinib, respectively. Erlotinib was dominated by afatinib and gefitinib. Compared to gefitinib, afatinib was associated with higher effectiveness (adjusted incremental quality-adjusted life-year: 0.21), higher total costs (adjusted incremental costs: $9745), and an incremental cost-effectiveness ratio of $46,506 per quality-adjusted life-year gained. Results from the sensitivity analyses indicated the findings of the base-case analysis were robust.

conclusionsContrary to previously published studies, our study established head-to-head comparisons of effectiveness and treatment-related costs of first-line EGFR-TKIs. Our findings suggest afatinib was the most cost-effective option among the three EGFR-TKIs.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsAfatinibAntineoplastic Combined Chemotherapy ProtocolsCost-Benefit AnalysisErbB ReceptorsErlotinib HydrochlorideGefitinibHumansMutationOntarioProtein Kinase InhibitorsAfatinibEGFR protein, humanErbB ReceptorsErlotinib HydrochlorideGefitinibProtein Kinase Inhibitors

Identifiers

PMID33786799
OpenAlexW3143019137

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.