Evidence map›Paper›PMID 39624385›Full record

ArticleERJ open research2024

Utility of adding oesophageal to endobronchial endosonography when staging lung cancer: a randomised trial.

Masahide Oki, Hideo Saka, Yukio Seki, Yoshihito Kogure, Hideyuki Niwa, Arisa Yamada, Atsushi Torii, Chiyoe Kitagawa, Masahiko Ando

Abstract read
In one paragraph

Article in ERJ open research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. 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

9 authors.

Masahide OkiDepartment of Respiratory Medicine, NHO Nagoya Medical Center, Nagoya, Japan.ORCID https://orcid.org/0000-0003-2164-238X
Hideo SakaDepartment of Respiratory Medicine, NHO Nagoya Medical Center, Nagoya, Japan.
Yukio SekiDepartment of Thoracic Surgery, NHO Nagoya Medical Center, Nagoya, Japan.
Yoshihito KogureDepartment of Respiratory Medicine, NHO Nagoya Medical Center, Nagoya, Japan.
Hideyuki NiwaDepartment of Respiratory Medicine, NHO Nagoya Medical Center, Nagoya, Japan.
Arisa YamadaDepartment of Respiratory Medicine, NHO Nagoya Medical Center, Nagoya, Japan.
Atsushi ToriiDepartment of Respiratory Medicine, NHO Nagoya Medical Center, Nagoya, Japan.
Chiyoe KitagawaDepartment of Respiratory Medicine, NHO Nagoya Medical Center, Nagoya, Japan.
Masahiko AndoDepartment of Advanced Medicine, Nagoya University Hospital, Nagoya, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Both combined endobronchial ultrasonography (EBUS) and transoesophageal bronchoscopic ultrasonography (EUS-B) and EBUS alone have been recommended for preoperative mediastinal staging of nonsmall cell lung cancer (NSCLC). However, no randomised study comparing these two methods has been published. The purpose of the present study was to compare the sensitivity of EBUS and that of combined EBUS and EUS-B (EBUS/EUS-B) in terms of detecting N2/N3 disease during staging of NSCLC. Methods: Patients with known or suspected, potentially operable NSCLC were recruited and randomised to undergo EBUS or EBUS/EUS-B under conscious sedation. The primary end-point was a comparison of the sensitivity of EBUS alone and EBUS/EUS-B. Results: A total of 240 patients were enrolled and randomised, among whom 219 (105 EBUS group; 114 EBUS/EUS-B group) were included in the analysis. The sensitivities of EBUS and EBUS/EUS-B in terms of detecting N2/N3 disease were 75.0% and 79.3% respectively (p=0.698). In the EBUS/EUS-B group, only EUS-B yielded diagnostic results in two patients; the sensitivity thus increased from 72.4% to 79.3% on addition of EUS-B to EBUS. Conclusions: The difference in the sensitivities of EBUS alone and EBUS/EUS-B in terms of diagnosing N2/N3 disease was not statistically significant. Although the increase in sensitivity with the addition of EUS-B is modest, it is maximised when EUS-B is used to sample lymph nodes not accessible by EBUS alone.

Identifiers

PMID39624385
PMCPMC11609961

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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.