Evidence map›Paper›PMID 36811822›Full record

ArticlePharmacoEconomics - open2023

Evaluation of Cost-Effectiveness of Adjuvant Osimertinib in Patients with Resected EGFR Mutation-Positive Non-small Cell Lung Cancer.

Andre Verhoek, Parneet Cheema, Barbara Melosky, Benoit Samson, Frances A Shepherd, Filippo de Marinis, Thomas John, Yi-Long Wu, Bart Heeg, Nadia Van Dalfsen and 4 more

2 registry-linked trialsOpen access · goldAbstract read
In one paragraph

Article in PharmacoEconomics - open, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
4.1field-weighted citation impact, top 6% 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.

NCT02296125 phase3completednot on this map

A Phase III, Double-blind, Randomised Study to Assess the Safety and Efficacy of AZD9291 Versus a Standard of Care Epidermal Growth Factor Receptor Tyrosine Kinase Inhibitor as First Line Treatment in Patients With Epidermal Growth Factor Receptor Mutation Positive, Locally Advanced or Metastatic Non Small Cell Lung Cancer.

TypeinterventionalSponsorAstraZenecaRan2014 to 2025Enrolled674ConditionsLocally Advanced or Metastatic EGFR Sensitising Mutation Positive Non Small Cell Lung CancerArmsAZD9291 80 mg/40 mg + placebo, Placebo Erlotinib 150/100mg, Placebo Gefitinib 250 mg, Erlotinib 150/100 mg, Gefitinib 250 mg
NCT02511106 phase3active not recruitingnot on this map

A Phase III, Double-blind, Randomized, Placebo-controlled Multi-centre, Study to Assess the Efficacy and Safety of AZD9291 Versus Placebo, in Patients With Epidermal Growth Factor Receptor Mutation Positive Stage IB-IIIA Non-small Cell Lung Carcinoma, Following Complete Tumour Resection With or Without Adjuvant Chemotherapy (ADAURA).

TypeinterventionalSponsorAstraZenecaRan2015 to 2029Enrolled682ConditionsStage IB-IIIA Non-small Cell Lung CarcinomaArmsAZD9291 80 mg/40 mg, Placebo AZD9291 80 mg/40 mg, Open-label AZD9291 80 mg/40 mg
3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 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

14 authors at 9 institutions in 6 countries.

Andre VerhoekCytel, Weena 316-318, 3012 NJ, Rotterdam, The Netherlands. andre.verhoek@cytel.com.ORCID http://orcid.org/0000-0003-3958-0033
Parneet CheemaWilliam Osler Health System, University of Toronto, Toronto, ON, Canada.
Barbara MeloskyDepartment of Medical Oncology, BC Cancer, Vancouver, BC, Canada.
Benoit SamsonCharles LeMoyne Hospital Cancer Center, Greenfield Park, QC, Canada.
Frances A ShepherdDepartment of Medical Oncology and Hematology, University Health Network, Princess Margaret Cancer Centre and the University of Toronto, Toronto, ON, Canada.
Filippo de MarinisDivision of Thoracic Oncology, European Institute of Oncology, IRCCS, Milan, Italy.
Thomas JohnDepartment of Medical Oncology, Austin Health, Melbourne, VIC, Australia.
Yi-Long WuDepartment of Oncology, Guangdong Lung Cancer Institute, Guangdong Provincial People's Hospital and Guangdong Academy of Medical Sciences, Guangzhou, People's Republic of China.
Bart HeegCytel, Weena 316-318, 3012 NJ, Rotterdam, The Netherlands.
Nadia Van DalfsenCytel, Weena 316-318, 3012 NJ, Rotterdam, The Netherlands.
Benjamin BrackeGlobal Health Economics and Payer Evidence, AstraZeneca, Cambridge, UK.
Miguel MirandaGlobal Medical Development, AstraZeneca, Cambridge, UK.
Simon ShawGlobal Medical Affairs, AstraZeneca, Cambridge, UK.
Daniel MoldaverHealth Economics and Payer Evidence, AstraZeneca, Mississauga, ON, Canada.
AstraZeneca (United Kingdom) · GBCytel (United States) · USAstraZeneca (Canada) · CAAustin Health · AUEuropean Institute of Oncology · ITGuangdong Academy of Medical Sciences · CNHôpital Charles-Le Moyne · CAUniversity Health Network · CAUniversity of Toronto · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFor many patients with resected epidermal growth factor receptor mutation-positive (EGFRm) non-small cell lung cancer (NSCLC), current standard of care (SoC) is adjuvant chemotherapy; however, disease recurrence remains high. Based on positive results from ADAURA (NCT02511106), adjuvant osimertinib was approved for treatment of resected stage IB‒IIIA EGFRm NSCLC.

objectiveThe aim was to assess the cost-effectiveness of adjuvant osimertinib in patients with resected EGFRm NSCLC.

methodsA five-health-state, state-transition model with time dependency was developed to estimate lifetime (38 years) costs and survival of resected EGFRm patients treated with adjuvant osimertinib or placebo (active surveillance), with/without prior adjuvant chemotherapy, using a Canadian Public Healthcare perspective. Transitions between health states were modeled using ADAURA and FLAURA (NCT02296125) data, Canadian life tables, and real-world data (CancerLinQ Discovery

resultsIn the reference case, adjuvant osimertinib treatment led to a mean 3.20 additional quality-adjusted life-years (QALYs; (11.77 vs 8.57) per patient, versus active surveillance. The modeled median percentage of patients alive at 10 years was 62.5% versus 39.3%, respectively. Osimertinib was associated with mean added costs of Canadian dollars (C$)114,513 per patient and a cost/QALY (incremental cost-effectiveness ratio) of C$35,811 versus active surveillance. Model robustness was demonstrated by scenario analyses.

conclusionsIn this cost-effectiveness assessment, adjuvant osimertinib was cost-effective compared with active surveillance for patients with completely resected stage IB‒IIIA EGFRm NSCLC after SoC.

Identifiers

PMID36811822
PMCPMC10169948
OpenAlexW4321490951

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

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.