Evidence map›Paper›PMID 36918817›Full record

ArticleBMC cancer2023

A text-mining approach to study the real-world effectiveness and potentially fatal immune-related adverse events of PD-1 and PD-L1 inhibitors in older patients with stage III/IV non-small cell lung cancer.

Hanieh Abedian Kalkhoran, Juliëtte Zwaveling, Bert N Storm, Sylvia A van Laar, Johanneke Ea Portielje, Henk Codrington, Dieuwke Luijten, Pepijn Brocken, Egbert F Smit, Loes E Visser

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Article in BMC cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Article
  3. Observational
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Use of proxy indicators for automated surveillance of severe acute respiratory infection, the Netherlands, 2017 to 2023: a proof-of-concept study.Euro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin · 2024
    Article
  10. Article
  11. 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

10 authors.

Hanieh Abedian KalkhoranDepartment of Clinical Pharmacy and Toxicology, Leiden University Medical Centre, Leiden, The Netherlands. h.abedian_kalkhoran@lumc.nl.
Juliëtte ZwavelingDepartment of Clinical Pharmacy and Toxicology, Leiden University Medical Centre, Leiden, The Netherlands.
Bert N StormDepartment of Pharmacy, Haga Teaching Hospital, The Hague, The Netherlands.
Sylvia A van LaarDepartment of Clinical Pharmacy and Toxicology, Leiden University Medical Centre, Leiden, The Netherlands.
Johanneke Ea PortieljeDepartment of Internal Medicine - Medical Oncology, Leiden University Medical Centre, Leiden, The Netherlands.
Henk CodringtonDepartment of Pulmonary Diseases - Pulmonic Oncology, Haga Teaching Hospital, The Hague, The Netherlands.
Dieuwke LuijtenDepartment of Pulmonary Diseases - Pulmonic Oncology, Haga Teaching Hospital, The Hague, The Netherlands.
Pepijn BrockenDepartment of Pulmonary Diseases - Pulmonic Oncology, Haga Teaching Hospital, The Hague, The Netherlands.
Egbert F SmitDepartment of Pulmonary Disease, Leiden University Medical Centre, Leiden, The Netherlands.
Loes E VisserDepartment of Pharmacy, Haga Teaching Hospital, The Hague, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis study was designed to investigate the impact of age on the effectiveness and immune-related adverse events (irAEs) of programmed death-(ligand)1 [PD-(L)1] inhibitors in patients with non-small cell lung cancer (NSCLC) using a novel text-mining technique.

methodsThis retrospective study included patients with stage III/IV NSCLC treated with a PD-(L)1 inhibitor (nivolumab, pembrolizumab, atezolizumab and durvalumab) at Leiden University Medical Centre and Haga Teaching hospital, (both in The Netherlands) from September 2016 to May 2021. All the relevant data was extracted from the structured and unstructured fields of the Electronic Health Records using a novel text-mining tool. Effectiveness [progression-free survival (PFS) and overall survival (OS)] and safety (the incidence of nine potentially fatal irAEs and systemic corticosteroid requirement) outcomes were compared across age subgroups (young: < 65 years, Middle-aged: 65-74 years, and old: ≥ 75 years) after adjustment for confounding.

resultsOf 689 patients, 310 patients (45.0%) were < 65 years, 275 patients (39.9%) were aged between 65 and 74 years, and 104 patients (15.1%) were ≥ 75 years. There was no significant difference between younger and older patients regarding PFS (median PFS 12, 8, 13 months respectively; Hazard ratio (HR)

conclusionsThe use of PD-(L)1 inhibitors is not associated with age related decrease of PFS and OS, nor with increased incidence of serious irAEs compared to younger patients receiving these treatments. Chronological age must therefore not be used as a predictor for the effectiveness or safety of ICIs.

Indexed as

Antineoplastic Agents, ImmunologicalCarcinoma, Non-Small-Cell LungLung NeoplasmsAgedHumansImmune Checkpoint InhibitorsMiddle AgedProgrammed Cell Death 1 ReceptorRetrospective StudiesAntineoplastic Agents, ImmunologicalImmune Checkpoint InhibitorsProgrammed Cell Death 1 ReceptorAnti-PD-(L)1 therapyElderlyImmune checkpoint inhibitor (ICI)Non-small cell lung cancer (NSCLC)Real-world

Identifiers

PMID36918817
PMCPMC10015929

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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.