Franseen needle in endobronchial ultrasound-guided transbronchial needle aspiration: a phase II prospective study

Author:

Shikano Kohei12ORCID,Ikari Jun12,Nakajima Takahiro3,Ota Masayuki42,Shiko Yuki56,Naito Akira12,Abe Mitsuhiro12,Kawasaki Takeshi12,Ikeda Jun-Ichiro42,Ozawa Yoshihito56,Suzuki Takuji12

Affiliation:

1. Department of Respirology , Graduate School of Medicine, , 1-8-1 Inohana, Chuo-Ku, Chiba , Japan

2. Chiba University , Graduate School of Medicine, , 1-8-1 Inohana, Chuo-Ku, Chiba , Japan

3. Department of General Thoracic Surgery, Dokkyo Medical University , 880 Kitakobayashi, Mibu, Shimotsuga, Tochigi , Japan

4. Department of Diagnostic Pathology , Graduate School of Medicine, , 1-8-1 Inohana, Chuo-Ku, Chiba , Japan

5. Biostatistics Section , Clinical Research Center, , 1-8-1 Inohana, Chuo-Ku, Chiba , Japan

6. Chiba University Hospital , Clinical Research Center, , 1-8-1 Inohana, Chuo-Ku, Chiba , Japan

Abstract

Abstract Background Endobronchial ultrasound-guided transbronchial needle aspiration (EBUS-TBNA) has been used to diagnose and stage lung cancer. Acquire™ Pulmonary and Expect™ Pulmonary dedicated EBUS-TBNA needles were introduced as the Franseen and Lancet needles, respectively. It is still unclear whether the Franseen or Lancet needles yield a higher quality specimen especially focusing on next-generation sequencing-based molecular testing. Methods A single-center, prospective study performed at the Chiba University Hospital randomly assigned patients to two groups: Group A, wherein the first and second EBUS-TBNA were performed using Lancet and Franseen needles, respectively, and Group B, wherein the first and second EBUS-TBNA were performed using Franseen and Lancet needles, respectively. Each specimen was compared and analyzed pathologically. The primary outcome was the histological tissue area except blood clot and the cellularity of each sample. We also examined the success rate of molecular testing. Results Twelve patients who underwent EBUS-TBNA between November 2022 and February 2023 were enrolled in this study. The tissue area of the specimens obtained by the Franseen and Lancet needles was 13.3 ± 6.4 mm2 and 10.6 ± 6.3 mm2, respectively (P = .355). The tumor cellularity in the specimens obtained using the Franseen and Lancet needles was 54.0 ± 30.3 and 46.2 ± 36.3%, respectively (P = .608). The success rate of molecular testing using the single-pass sample by Franseen needle was 85.7 and 57.1% by Lancet needle. No serious complications were reported. Conclusions The Franseen needle tended to show a greater amount of specimen with higher tumor cellularity than the Lancet needle which may contribute higher success rate of molecular testing. Further studies must be conducted to validate the results of this study. Key findings What is known and what is new?  What is the implication, and what should change now? 

Funder

Chiba Foundation for Health Promotion & Disease Prevention

Publisher

Oxford University Press (OUP)

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3