Evidence map›Paper›PMID 39195310›Full record

ArticleCurrent oncology (Toronto, Ont.)2024

Real-World Treatment Patterns, Health Outcomes, and Healthcare Resource Use in Advanced Common EGFR-Positive Non-Small Cell Lung Cancer Patients Treated with Osimertinib in Alberta.

Winson Y Cheung, Chantelle Carbonell, Vishal Navani, Randeep S Sangha, Emmanuel M Ewara, Julia Elia-Pacitti, Sandra Iczkovitz, Tamer N Jarada, Matthew T Warkentin

Abstract read
In one paragraph

Article in Current oncology (Toronto, Ont.), 2024. 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
–field-weighted citation impact
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.

  1. Observational
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

9 authors.

Winson Y CheungDepartment of Oncology, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 1N4, Canada.
Chantelle CarbonellDepartment of Oncology, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 1N4, Canada.ORCID 0009-0004-6384-3424
Vishal NavaniDepartment of Oncology, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 1N4, Canada.
Randeep S SanghaDepartment of Oncology, Faculty of Medicine & Dentistry, University of Alberta, Edmonton, AB T6G 2R3, Canada.
Emmanuel M EwaraJohnson & Johnson Innovative Medicine, Toronto, ON M3C 1L9, Canada.
Julia Elia-PacittiJohnson & Johnson Innovative Medicine, Toronto, ON M3C 1L9, Canada.
Sandra IczkovitzJohnson & Johnson Innovative Medicine, Toronto, ON M3C 1L9, Canada.
Tamer N JaradaDepartment of Oncology, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 1N4, Canada.ORCID 0000-0002-9390-1742
Matthew T WarkentinDepartment of Oncology, Cumming School of Medicine, University of Calgary, Calgary, AB T2N 1N4, Canada.

Funding

Janssen Inc. Canada N/A
6 · The paper itself

Abstract

There is limited information on the treatment trajectory and outcomes of patients with advanced cEGFRm NSCLC treated with osimertinib in routine clinical practice in Canada. By using and analyzing population-based administrative data and detailed chart abstraction in the province of Alberta, our objective was to capture Canadian-specific real-world treatment patterns, health outcomes, and healthcare resource utilization (HCRU) in advanced cEGFRm NSCLC patients who were (a) treated with osimertinib and (b) those receiving treatment after osimertinib. In our study cohort, we found that the overall survival rates for real-world patients receiving osimertinib were less favorable than those observed in clinical trials (24.0 versus 38.6 months). The attrition rate after osimertinib was substantial and high HCRU persisted across many years after diagnosis and treatment. This study provides important real-world evidence on contemporary survival, treatment patterns, and healthcare use among cEGFRm NSCLC patients treated with osimertinib and suggests that further research efforts are needed to improve therapeutic options in both the first and subsequent line settings.

Indexed as

AcrylamidesAniline CompoundsCarcinoma, Non-Small-Cell LungErbB ReceptorsLung NeoplasmsAgedAged, 80 and overAlbertaAntineoplastic AgentsFemaleHumansIndolesMaleMiddle AgedPyrimidinesTreatment OutcomeAcrylamidesAniline CompoundsAntineoplastic AgentsEGFR protein, humanErbB ReceptorsIndolesosimertinibPyrimidinesadvanced diseasenon-small cell lung cancerosimertiniboutcomestreatment

Identifiers

PMID39195310
PMCPMC11352775

What OpenQuestion holds

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LicenceCC BY
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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.