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Comparison of the slow‐pull and aspiration methods of endobronchial ultrasound‐guided transbronchial needle aspiration for next‐generation sequencing‐compatible tissue collection in non‐small cell lung cancer

BACKGROUND: Personalized treatment for non‐small cell lung cancer (NSCLC) has advanced rapidly, and elucidating the genetic changes that trigger this disease is crucial for appropriate treatment selection. Both slow‐pull and aspiration methods of endobronchial ultrasound‐guided transbronchial needle...

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Autores principales: Kajita, Yukihito, Teranishi, Shuhei, Sawazumi, Tomoe, Watanabe, Haruka, Nagaoka, Satoshi, Tanaka, Anna, Suzukawa, Yuichirou, Motobayashi, Yuto, Hirose, Tomofumi, Maeda, Chihiro, Seki, Kenichi, Tashiro, Ken, Kobayashi, Nobuaki, Yamamoto, Masaki, Kudo, Makoto, Inayama, Yoshiaki, Kaneko, Takeshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10587950/
https://www.ncbi.nlm.nih.gov/pubmed/37732488
http://dx.doi.org/10.1002/cam4.6561
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author Kajita, Yukihito
Teranishi, Shuhei
Sawazumi, Tomoe
Watanabe, Haruka
Nagaoka, Satoshi
Tanaka, Anna
Suzukawa, Yuichirou
Motobayashi, Yuto
Hirose, Tomofumi
Maeda, Chihiro
Seki, Kenichi
Tashiro, Ken
Kobayashi, Nobuaki
Yamamoto, Masaki
Kudo, Makoto
Inayama, Yoshiaki
Kaneko, Takeshi
author_facet Kajita, Yukihito
Teranishi, Shuhei
Sawazumi, Tomoe
Watanabe, Haruka
Nagaoka, Satoshi
Tanaka, Anna
Suzukawa, Yuichirou
Motobayashi, Yuto
Hirose, Tomofumi
Maeda, Chihiro
Seki, Kenichi
Tashiro, Ken
Kobayashi, Nobuaki
Yamamoto, Masaki
Kudo, Makoto
Inayama, Yoshiaki
Kaneko, Takeshi
author_sort Kajita, Yukihito
collection PubMed
description BACKGROUND: Personalized treatment for non‐small cell lung cancer (NSCLC) has advanced rapidly, and elucidating the genetic changes that trigger this disease is crucial for appropriate treatment selection. Both slow‐pull and aspiration methods of endobronchial ultrasound‐guided transbronchial needle aspiration (EBUS‐TBNA) are accepted methods for collecting samples suitable for next‐generation sequencing (NGS) to examine driver gene mutations and translocations in NSCLC. Here, we aimed to determine which of these two methods is superior for obtaining higher‐quality samples from patients with NSCLC. METHODS: Seventy‐one patients diagnosed with NSCLC via EBUS‐TBNA using the slow‐pull or aspiration (20‐mL negative pressure) methods between July 2019 and September 2022 were included. A total of 203 tissue samples from the 71 patients were fixed in formalin, embedded in paraffin, and mounted on slides. The presence of tissue cores, degree of blood contamination, and number of tumor cells were compared between the groups. The success rate of NGS, using Oncomine Dx Target Test Multi‐CDx, was also compared between the groups. RESULTS: The slow‐pull method was associated with a higher yield of tissue cores, lower degree of blood contamination, and higher number of tumor cells than the aspiration method. The success rate of the NGS was also significantly higher for the slow‐pull group (95%) than for the aspiration group (68%). CONCLUSION: Overall, these findings suggest that the slow‐pull method is a superior technique for EBUS‐TBNA to obtain high‐quality tissue samples for NGS. The slow‐pull method may contribute to the identification of driver gene mutations and translocations and facilitate personalized treatment of NSCLC.
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spelling pubmed-105879502023-10-21 Comparison of the slow‐pull and aspiration methods of endobronchial ultrasound‐guided transbronchial needle aspiration for next‐generation sequencing‐compatible tissue collection in non‐small cell lung cancer Kajita, Yukihito Teranishi, Shuhei Sawazumi, Tomoe Watanabe, Haruka Nagaoka, Satoshi Tanaka, Anna Suzukawa, Yuichirou Motobayashi, Yuto Hirose, Tomofumi Maeda, Chihiro Seki, Kenichi Tashiro, Ken Kobayashi, Nobuaki Yamamoto, Masaki Kudo, Makoto Inayama, Yoshiaki Kaneko, Takeshi Cancer Med RESEARCH ARTICLES BACKGROUND: Personalized treatment for non‐small cell lung cancer (NSCLC) has advanced rapidly, and elucidating the genetic changes that trigger this disease is crucial for appropriate treatment selection. Both slow‐pull and aspiration methods of endobronchial ultrasound‐guided transbronchial needle aspiration (EBUS‐TBNA) are accepted methods for collecting samples suitable for next‐generation sequencing (NGS) to examine driver gene mutations and translocations in NSCLC. Here, we aimed to determine which of these two methods is superior for obtaining higher‐quality samples from patients with NSCLC. METHODS: Seventy‐one patients diagnosed with NSCLC via EBUS‐TBNA using the slow‐pull or aspiration (20‐mL negative pressure) methods between July 2019 and September 2022 were included. A total of 203 tissue samples from the 71 patients were fixed in formalin, embedded in paraffin, and mounted on slides. The presence of tissue cores, degree of blood contamination, and number of tumor cells were compared between the groups. The success rate of NGS, using Oncomine Dx Target Test Multi‐CDx, was also compared between the groups. RESULTS: The slow‐pull method was associated with a higher yield of tissue cores, lower degree of blood contamination, and higher number of tumor cells than the aspiration method. The success rate of the NGS was also significantly higher for the slow‐pull group (95%) than for the aspiration group (68%). CONCLUSION: Overall, these findings suggest that the slow‐pull method is a superior technique for EBUS‐TBNA to obtain high‐quality tissue samples for NGS. The slow‐pull method may contribute to the identification of driver gene mutations and translocations and facilitate personalized treatment of NSCLC. John Wiley and Sons Inc. 2023-09-21 /pmc/articles/PMC10587950/ /pubmed/37732488 http://dx.doi.org/10.1002/cam4.6561 Text en © 2023 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle RESEARCH ARTICLES
Kajita, Yukihito
Teranishi, Shuhei
Sawazumi, Tomoe
Watanabe, Haruka
Nagaoka, Satoshi
Tanaka, Anna
Suzukawa, Yuichirou
Motobayashi, Yuto
Hirose, Tomofumi
Maeda, Chihiro
Seki, Kenichi
Tashiro, Ken
Kobayashi, Nobuaki
Yamamoto, Masaki
Kudo, Makoto
Inayama, Yoshiaki
Kaneko, Takeshi
Comparison of the slow‐pull and aspiration methods of endobronchial ultrasound‐guided transbronchial needle aspiration for next‐generation sequencing‐compatible tissue collection in non‐small cell lung cancer
title Comparison of the slow‐pull and aspiration methods of endobronchial ultrasound‐guided transbronchial needle aspiration for next‐generation sequencing‐compatible tissue collection in non‐small cell lung cancer
title_full Comparison of the slow‐pull and aspiration methods of endobronchial ultrasound‐guided transbronchial needle aspiration for next‐generation sequencing‐compatible tissue collection in non‐small cell lung cancer
title_fullStr Comparison of the slow‐pull and aspiration methods of endobronchial ultrasound‐guided transbronchial needle aspiration for next‐generation sequencing‐compatible tissue collection in non‐small cell lung cancer
title_full_unstemmed Comparison of the slow‐pull and aspiration methods of endobronchial ultrasound‐guided transbronchial needle aspiration for next‐generation sequencing‐compatible tissue collection in non‐small cell lung cancer
title_short Comparison of the slow‐pull and aspiration methods of endobronchial ultrasound‐guided transbronchial needle aspiration for next‐generation sequencing‐compatible tissue collection in non‐small cell lung cancer
title_sort comparison of the slow‐pull and aspiration methods of endobronchial ultrasound‐guided transbronchial needle aspiration for next‐generation sequencing‐compatible tissue collection in non‐small cell lung cancer
topic RESEARCH ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10587950/
https://www.ncbi.nlm.nih.gov/pubmed/37732488
http://dx.doi.org/10.1002/cam4.6561
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