Evidence map›Paper›PMID 40426148›Full record

ArticleBMC pulmonary medicine2025

Real-world treatment patterns and outcomes for patients with non-metastatic non-small cell lung cancer: retrospective analyses in Canada, England, and Germany.

Alastair Greystoke, Melinda J Daumont, Caroline Rault, Hannah Baltus, Philip Q Ding, Gabrielle Emanuel, Stefano Lucherini, Lien Vo, Valeria M Saglimbene, Eleanor Ralphs and 5 more

Abstract read
In one paragraph

Article in BMC pulmonary medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
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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

15 authors.

Alastair Greystoke *Newcastle Hospital and Newcastle University, Newcastle Upon Tyne, UK. alastair.greystoke@newcastle.ac.uk.
Melinda J DaumontWorldwide Health Economics & Outcomes Research, Bristol Myers Squibb, Braine-L'Alleud, Belgium.
Caroline RaultData Gnosis, Rennes, France.
Hannah Baltus *Institute for Social Medicine and Epidemiology, University of Lübeck, Lübeck, Germany.
Philip Q DingDepartment of Oncology, University of Calgary, Oncology Outcomes, Calgary, AB, Canada.
Gabrielle EmanuelReal World Data Analytics Markets, Bristol Myers Squibb, Uxbridge, UK.
Stefano LucheriniWorldwide Health Economics & Outcomes Research, Bristol Myers Squibb, Uxbridge, UK.
Lien VoWorldwide Health Economics & Outcomes Research, Bristol Myers Squibb, Princeton, NJ, USA.
Valeria M SaglimbeneReal World Solutions, IQVIA Ltd, Milan, Italy.
Eleanor RalphsReal World Solutions, IQVIA Ltd, London, UK.
Cátia LealReal World Solutions, IQVIA Ltd, Lisbon, Portugal.
Minouk J SchoemakerReal World Solutions, IQVIA Ltd, Amsterdam, Netherlands.
Alexander KatalinicInstitute for Social Medicine and Epidemiology, University of Lübeck, Lübeck, Germany.
Annika Waldmann *Institute for Social Medicine and Epidemiology, University of Lübeck, Lübeck, Germany.
Winson Y Cheung *Department of Oncology, University of Calgary, Oncology Outcomes, Calgary, AB, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRecent therapeutic advancements for non-metastatic non-small cell lung cancer (NSCLC) have increased the need for real-world baselines against which future changes in patient management and clinical outcomes can be compared.

methodsData on patient characteristics, initial treatment, and overall survival (OS) were derived from adult patients diagnosed with stage I-IIIC NSCLC (2010-2020) in a regional Canadian database (Oncology Outcomes [O2]), an English national registry (Cancer Analysis System [CAS]), and four regional German registries (VONKOdb) and retrospectively analyzed separately using analogous methodology.

resultsData from 85,433 patients were analyzed. Stage at diagnosis varied, with proportions with stage I NSCLC ranging from 30.9% (VONKOdb) to 44.2% (O2) and with stage III disease from 36.9% (O2) to 48.5% (VONKOdb). Across the data sources, proportions receiving surgery ± other treatments were similar for stages I and II, but decreased through stages IIIA, IIIB, and IIIC (range, 24.7-42.7%, 4.6-21.8%, and 0.9-7.5%, respectively). Overall, 70.3-85.2% of patients received active treatment for NSCLC, with a trend toward lower proportions among those with stage III disease. Reached median OS tended to be longest in patients with resected stage I/II NSCLC (range, 28.8-128.0 months) and shortest in patients with stage IIIB/IIIC disease treated with systemic anticancer therapy (SACT) alone, radiotherapy alone, or SACT + palliative radiotherapy (range, 4.8-21.2 months).

conclusionsThese data provide insights into treatment pathways and survival outcomes before the widespread use of immunotherapy-based and targeted therapies and will serve as an important baseline for future evaluations of emerging treatments for patients with non-metastatic NSCLC.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsAdultAgedAged, 80 and overCanadaEnglandFemaleGermanyHumansMaleMiddle AgedNeoplasm StagingRegistriesRetrospective StudiesTreatment OutcomeDatabaseI-O OptimiseReal-world evidenceRegistriesSurvivalTreatment patterns

Identifiers

PMID40426148
PMCPMC12107783

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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.