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Lymphadenopathy Tissue Sampling by EUS-Guided Fine-Needle Biopsy Contributes to Meeting the Conditions for Genomic Profiling.
Sugimoto, Mitsuru; Takagi, Tadayuki; Suzuki, Rei; Konno, Naoki; Asama, Hiroyuki; Sato, Yuki; Irie, Hiroki; Nakamura, Jun; Takasumi, Mika; Hashimoto, Minami; Kato, Tsunetaka; Hashimoto, Yuko; Hikichi, Takuto; Ohira, Hiromasa.
Afiliação
  • Sugimoto M; Department of Gastroenterology, School of Medicine.
  • Takagi T; Department of Gastroenterology, School of Medicine.
  • Suzuki R; Department of Gastroenterology, School of Medicine.
  • Konno N; Department of Gastroenterology, School of Medicine.
  • Asama H; Department of Gastroenterology, School of Medicine.
  • Sato Y; Department of Gastroenterology, School of Medicine.
  • Irie H; Department of Gastroenterology, School of Medicine.
  • Nakamura J; Department of Gastroenterology, School of Medicine.
  • Takasumi M; Department of Endoscopy, Fukushima Medical University Hospital.
  • Hashimoto M; Department of Gastroenterology, School of Medicine.
  • Kato T; Department of Endoscopy, Fukushima Medical University Hospital.
  • Hashimoto Y; Department of Gastroenterology, School of Medicine.
  • Hikichi T; Department of Endoscopy, Fukushima Medical University Hospital.
  • Ohira H; Department of Gastroenterology, School of Medicine.
J Clin Gastroenterol ; 2024 Jul 17.
Article em En | MEDLINE | ID: mdl-39042483
ABSTRACT
BACKGROUND AND

AIMS:

EUS-guided fine-needle biopsy (EUS-FNB) performed with a Franseen needle or Fork-tip needle enables greater tissue acquisition. However, it is unknown whether EUS-FNB could contribute to lymphadenopathy genomic profiling. The aim of this study was to determine the efficacy of EUS-FNB using a Franseen or Fork-tip needle for tissue acquisition and genomic profiling in patients with lymphadenopathy. PATIENTS AND

METHODS:

Patients with abdominal lymphadenopathy who underwent EUS-guided fine needle aspiration (FNA)/EUS-FNB were included in this study. The amount of acquired tissue and its suitability for genomic profiling were compared between FNA and FNB. Specimen quality was evaluated by a widely used pathologic adequacy scoring system (0 insufficient; 1 to 2 cytologic; 3 limited histologic; 4 to 5 sufficient histologic). The criteria of FoundationOne CDx (F1CDx) and NCC Oncopanel (NOP) were used to assess the suitability for genomic profiling.

RESULTS:

In total, 72 patients underwent EUS-FNA, and the other 20 patients underwent EUS-FNB. The pathologic adequacy score and suitability for genomic profiling based on the criteria were significantly higher for FNB than for FNA [histologic adequacy score 5 (4 to 5) versus 3 (0 to 5), P<0.01; F1CDx 16.7% vs. 0%, P=0.01; NOP 66.7% vs. 7.5%, P<0.01]. In multivariate analysis, EUS-FNB was identified as the only factor that influenced the suitability for genomic profiling based on the above-mentioned criteria (odds ratio 19.5, 95% CI 3.74-102, P<0.01).

CONCLUSIONS:

EUS-FNB performed using Franseen or Fork-tip needles may result in greater lymphadenopathy tissue acquisition and thus enhanced suitability for genomic profiling compared with EUS-FNA.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article