Transbronchial mediastinal cryobiopsy in the diagnosis of mediastinal lesions: a randomised trial.


Journal

The European respiratory journal
ISSN: 1399-3003
Titre abrégé: Eur Respir J
Pays: England
ID NLM: 8803460

Informations de publication

Date de publication:
12 2021
Historique:
received: 08 01 2021
accepted: 27 04 2021
pubmed: 8 5 2021
medline: 11 1 2022
entrez: 7 5 2021
Statut: epublish

Résumé

Guidelines recommend endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA) as an initial investigatory technique for mediastinal nodal staging in lung cancer. However, EBUS-TBNA can be limited by the inadequacy of intact tissues, which might restrict its diagnostic yield in mediastinal lesions of certain aetiologies. We have previously shown that EBUS-guided transbronchial mediastinal cryobiopsy can provide intact samples with greater volume. This randomised study determined the diagnostic yield and safety of transbronchial mediastinal cryobiopsy monitored by endosonography for the diagnosis of mediastinal lesions. Patients with a mediastinal lesion of ≥1 cm in the short axis were recruited. Following identification of the mediastinal lesion by linear EBUS, fine-needle aspiration and cryobiopsy were sequentially performed in a randomised order. Primary end-points were diagnostic yield, defined as the percentage of patients for whom mediastinal biopsy provided a definite diagnosis, and procedure-related adverse events. In total, 197 patients were enrolled and randomly allocated. The overall diagnostic yield was 79.9% and 91.8% for TBNA and transbronchial mediastinal cryobiopsy, respectively (p=0.001). Diagnostic yields were similar for metastatic lymphadenopathy (94.1% Transbronchial cryobiopsy performed under EBUS guidance is a safe and useful approach that offers diagnostic histological samples of mediastinal lesions.

Sections du résumé

BACKGROUND
Guidelines recommend endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA) as an initial investigatory technique for mediastinal nodal staging in lung cancer. However, EBUS-TBNA can be limited by the inadequacy of intact tissues, which might restrict its diagnostic yield in mediastinal lesions of certain aetiologies. We have previously shown that EBUS-guided transbronchial mediastinal cryobiopsy can provide intact samples with greater volume.
METHODS
This randomised study determined the diagnostic yield and safety of transbronchial mediastinal cryobiopsy monitored by endosonography for the diagnosis of mediastinal lesions. Patients with a mediastinal lesion of ≥1 cm in the short axis were recruited. Following identification of the mediastinal lesion by linear EBUS, fine-needle aspiration and cryobiopsy were sequentially performed in a randomised order. Primary end-points were diagnostic yield, defined as the percentage of patients for whom mediastinal biopsy provided a definite diagnosis, and procedure-related adverse events.
RESULTS
In total, 197 patients were enrolled and randomly allocated. The overall diagnostic yield was 79.9% and 91.8% for TBNA and transbronchial mediastinal cryobiopsy, respectively (p=0.001). Diagnostic yields were similar for metastatic lymphadenopathy (94.1%
CONCLUSIONS
Transbronchial cryobiopsy performed under EBUS guidance is a safe and useful approach that offers diagnostic histological samples of mediastinal lesions.

Identifiants

pubmed: 33958432
pii: 13993003.00055-2021
doi: 10.1183/13993003.00055-2021
pii:
doi:

Banques de données

ChiCTR
['ChiCTR1900025531']

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Commentaires et corrections

Type : CommentIn
Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright ©The authors 2021. For reproduction rights and permissions contact permissions@ersnet.org.

Déclaration de conflit d'intérêts

Conflict of interest: J. Zhang has nothing to disclose. Conflict of interest: J-R. Guo has nothing to disclose. Conflict of interest: Z-S. Huang has nothing to disclose. Conflict of interest: W-L. Fu has nothing to disclose. Conflict of interest: N. Wu has nothing to disclose. Conflict of interest: X-L. Wu has nothing to disclose. Conflict of interest: W.M. Kuebler has nothing to disclose. Conflict of interest: F.J.F. Herth reports personal fees for advisory board activities and lecture fees from Pulmonx, Erbe, Olympus and Uptake, outside the submitted work. Conflict of interest: Y. Fan has nothing to disclose.

Auteurs

Jing Zhang (J)

Dept of Respiratory Disease, Xinqiao Hospital, Third Military Medical University, Chongqing, China.

Jie-Ru Guo (JR)

Dept of Respiratory Disease, Xinqiao Hospital, Third Military Medical University, Chongqing, China.

Zan-Sheng Huang (ZS)

Dept of Respiratory Disease, Xinqiao Hospital, Third Military Medical University, Chongqing, China.

Wan-Lei Fu (WL)

Dept of Pathology, Xinqiao Hospital, Third Military Medical University, Chongqing, China.

Xian-Li Wu (XL)

Dept of Respiratory Disease, Xinqiao Hospital, Third Military Medical University, Chongqing, China.

Na Wu (N)

Dept of Epidemiology, College of Preventive Medicine, Third Military Medical University, Chongqing, China.

Wolfgang M Kuebler (WM)

Institute of Physiology, Charité Universitätsmedizin, Berlin, Germany.

Felix J F Herth (FJF)

Dept of Pneumology and Critical Care Medicine, Thoraxklinik, University of Heidelberg, Heidelberg, Germany.
Translational Lung Research Center Heidelberg, University of Heidelberg, Heidelberg, Germany.
Felix J.F. Herth and Ye Fan contributed equally to this article as lead authors and supervised the work.

Ye Fan (Y)

Dept of Respiratory Disease, Xinqiao Hospital, Third Military Medical University, Chongqing, China fanye2008728@googlemail.com.
Felix J.F. Herth and Ye Fan contributed equally to this article as lead authors and supervised the work.

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