Evidence map›Paper›PMID 35108331›Full record

ArticlePloS one2022

Feasibility of EBUS-TBNA for histopathological and molecular diagnostics of NSCLC-A retrospective single-center experience.

Marija Karadzovska-Kotevska, Hans Brunnström, Jaroslaw Kosieradzki, Lars Ek, Christel Estberg, Johan Staaf, Stefan Barath, Maria Planck

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 13% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Feasibility of EBUS-TBNA for the molecular characterization of non-small cell lung cancer.Jornal brasileiro de pneumologia : publicacao oficial da Sociedade Brasileira de Pneumologia e Tisilogia · 2024
    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

8 authors at 2 institutions in 1 country.

Marija Karadzovska-KotevskaDepartment of Respiratory Diseases and Allergology, Skåne University Hospital Lund, Lund, Sweden.ORCID 0000-0001-8104-0212
Hans BrunnströmDivision of Laboratory Medicine, Department of Genetics and Pathology, Region Skåne, Lund, Sweden.ORCID 0000-0001-7402-138X
Jaroslaw KosieradzkiDepartment of Respiratory Diseases and Allergology, Skåne University Hospital Lund, Lund, Sweden.
Lars EkDepartment of Respiratory Diseases and Allergology, Skåne University Hospital Lund, Lund, Sweden.
Christel EstbergDepartment of Respiratory Diseases and Allergology, Skåne University Hospital Lund, Lund, Sweden.
Johan StaafDivision of Oncology, Department of Clinical Sciences Lund, Lund University, Medicon Village, Lund, Sweden.
Stefan BarathDepartment of Respiratory Diseases and Allergology, Skåne University Hospital Lund, Lund, Sweden.
Maria PlanckDepartment of Respiratory Diseases and Allergology, Skåne University Hospital Lund, Lund, Sweden.
Lund University · SESkåne University Hospital · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA) is a minimally invasive bronchoscopic procedure, well established as a diagnostic modality of first choice for diagnosis and staging of non-small cell lung cancer (NSCLC). The therapeutic decisions for advanced NSCLC require comprehensive profiling of actionable mutations, which is currently considered to be an essential part of the diagnostic process. The purpose of this study was to evaluate the utility of EBUS-TBNA cytology specimen for histological subtyping, molecular profiling of NSCLC by massive parallel sequencing (MPS), as well as for PD-L1 analysis. A retrospective review of 806 EBUS bronchoscopies was performed, resulting in a cohort of 132 consecutive patients with EBUS-TBNA specimens showing NSCLC cells in lymph nodes. Data on patient demographics, radiology features of the suspected tumor and mediastinal engagement, lymph nodes sampled, the histopathological subtype of NSCLC, and performed molecular analysis were collected. The EBUS-TBNA specimen proved sufficient for subtyping NSCLC in 83% and analysis of treatment predictive biomarkers in 77% (MPS in 53%). The adequacy of the EBUS-TBNA specimen was 69% for EGFR gene mutation analysis, 49% for analysis of ALK rearrangement, 36% for ROS1 rearrangement, and 33% for analysis of PD-L1. The findings of our study confirm that EBUS-TBNA cytology aspirate is appropriate for diagnosis and subtyping of NSCLC and largely also for treatment predictive molecular testing, although more data is needed on the utility of EBUS cytology specimen for MPS and PD-L1 analysis.

Indexed as

Gene RearrangementMutationAgedBiomarkers, TumorBronchoscopyCarcinoma, Non-Small-Cell LungEndoscopic Ultrasound-Guided Fine Needle AspirationFeasibility StudiesFemaleFollow-Up StudiesHumansLung NeoplasmsMaleNeoplasm Recurrence, LocalPathology, MolecularPrognosisBiomarkers, Tumor

Identifiers

PMID35108331
PMCPMC8809531
OpenAlexW4210647599

What OpenQuestion holds

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Registered trials

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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.