Evidence map›Paper›PMID 35681723›Full record

ArticleCancers2022

Extracellular Vesicle-Based Bronchoalveolar Lavage Fluid Liquid Biopsy for EGFR Mutation Testing in Advanced Non-Squamous NSCLC.

In Ae Kim, Jae Young Hur, Hee Joung Kim, Wan Seop Kim, Kye Young Lee

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

Article in Cancers, 2022. 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 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 7% 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.

NCT05469022 phase2recruitingnot on this map

A Phase II, Single-Center, Single-Arm, Prospective Study of Neoadjuvant Lazertinib Therapy in Resectable EGFR-Mutation Positive Lung Adenocarcinoma Patients Detected by Broncho-alveolar Lavage Fluid(BALF) Liquid Biopsy

TypeinterventionalSponsorKonkuk University Medical CenterRan2022 to 2027Enrolled40ConditionsNon Small Cell Lung CancerArmsNeoadjuvant lazertinib
NCT07331701 not yet recruitingnot on this mapstarted 2026, after this paper: background citation

Association of BAL Fluid T-Cell Immune Activity With Tumor PD-L1 Expression and Its Prognostic Value: A Prospective Observational Study

Typeobservational_patient_registrySponsorSeoul National University HospitalRan2026 to 2027Enrolled60ConditionsLung Neoplasms, Tumor Immune Microenvironment
3 · Its place in the literature

Who cites it

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Roles of Exosomes in Chronic Rhinosinusitis: A Systematic Review.International journal of molecular sciences · 2022
    Pooled it
  2. Bronchoalveolar lavage fluidTranslational lung cancer research · 2026
    Article
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  4. Article
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  8. Article
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  15. A prospective phase 2 study of expeditiousTranslational lung cancer research · 2023
    Article
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  19. 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

5 authors at 2 institutions in 1 country.

In Ae KimPrecision Medicine Lung Cancer Center, Konkuk University Medical Center, Seoul 05030, Korea.ORCID 0000-0002-8994-2891
Jae Young HurPrecision Medicine Lung Cancer Center, Konkuk University Medical Center, Seoul 05030, Korea.ORCID 0000-0001-6105-9899
Hee Joung KimPrecision Medicine Lung Cancer Center, Konkuk University Medical Center, Seoul 05030, Korea.
Wan Seop KimPrecision Medicine Lung Cancer Center, Konkuk University Medical Center, Seoul 05030, Korea.ORCID 0000-0001-7704-5942
Kye Young LeePrecision Medicine Lung Cancer Center, Konkuk University Medical Center, Seoul 05030, Korea.ORCID 0000-0003-4687-5593
Konkuk University · KRKonkuk University Medical Center · KR

Funding

Chong Kun Dang Pharmaceutical Corp. KUH1010868
6 · The paper itself

Abstract

To overcome the limitations of the tissue biopsy and plasma cfDNA liquid biopsy, we performed the EV-based BALF liquid biopsy of 224 newly diagnosed stage III-IV NSCLC patients and compared it with tissue genotyping and 110 plasma liquid biopsies. Isolation of EVs from BALF was performed by ultracentrifugation. EGFR genotyping was performed through peptide nucleic acid clamping-assisted fluorescence melting curve analysis. Compared with tissue-based genotyping, BALF liquid biopsy demonstrated a sensitivity, specificity, and concordance rates of 97.8%, 96.9%, and 97.7%, respectively. The performance of BALF liquid biopsy was almost identical to that of standard tissue-based genotyping. In contrast, plasma cfDNA-based liquid biopsy (n = 110) demonstrated sensitivity, specificity, and concordance rates of 48.5%, 86.3%, and 63.6%, respectively. The mean turn-around time of BALF liquid biopsy was significantly shorter (2.6 days) than that of tissue-based genotyping (13.9 days; p < 0.001). Therefore, the use of EV-based BALF shortens the time for confirmation of EGFR mutation status for starting EGFR-TKI treatment and can hence potentially improve clinical outcomes. As a result, we suggest that EV-based BALF EGFR testing in advanced lung NSCLC is a highly accurate rapid method and can be used as an alternative method for lung tissue biopsy.

Indexed as

bronchoalveolar lavage (BAL)EGFR mutation testingextracellular vesiclesliquid biopsyNSCLC

Identifiers

PMID35681723
PMCPMC9179452
OpenAlexW4281841133

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.