Liquid biopsy of wash samples obtained via endoscopic ultrasound-guided fine-needle biopsy: Comparison with liquid biopsy of plasma in pancreatic cancer.

genomics liquid biopsy mutation neoplasms oncogenes pancreas

Journal

Diagnostic cytopathology
ISSN: 1097-0339
Titre abrégé: Diagn Cytopathol
Pays: United States
ID NLM: 8506895

Informations de publication

Date de publication:
22 Mar 2024
Historique:
revised: 11 03 2024
received: 17 02 2024
accepted: 13 03 2024
medline: 22 3 2024
pubmed: 22 3 2024
entrez: 22 3 2024
Statut: aheadofprint

Résumé

Pancreatic cancer (PC) has a poor prognosis and limited treatment options. Liquid biopsy, which analyzes circulating tumor DNA (ctDNA) in blood, holds promise for precision medicine; however, low ctDNA detection rates pose challenges. This study aimed to investigate the utility of wash samples obtained via endoscopic ultrasound-guided fine-needle biopsy (EUS-FNB) as a liquid biopsy for PC. A total of 166 samples (42 formalin-fixed paraffin-embedded [FFPE] tissues, 80 wash samples, and 44 plasma samples) were collected from 48 patients with PC for genomic analysis. DNA was extracted and quantified, and 60 significantly mutated genes were sequenced. The genomic profiles of FFPE tissues, wash samples, and plasma samples were compared. Finally, the ability to detect druggable mutations in 80 wash samples and 44 plasma samples was investigated. The amount of DNA was significantly lower in plasma samples than in wash samples. Genomic analysis revealed a higher detection rate of oncogenic mutations in FFPE tissues (98%) and wash samples (96%) than in plasma samples (18%) and a comparable detection rate in FFPE tissues and wash samples. Tumor-derived oncogenic mutations were detected more frequently in wash samples than in plasma samples. Furthermore, the oncogenic mutations detection rate remained high in wash samples at all PC stages but low in plasma samples even at advanced PC stages. Using wash samples was more sensitive than plasma samples for identifying oncogenic and druggable mutations. The wash sample obtained via EUS-FNB is an ideal specimen for use as a liquid biopsy for PC.

Identifiants

pubmed: 38516904
doi: 10.1002/dc.25306
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Uehara Memorial Foundation
Organisme : Takeda Science Foundation
Organisme : Japan Society for the Promotion of Science
Organisme : Pancreas Research Foundation of Japan
Organisme : Chiba Foundation for Health Promotion and Disease Prevention
Organisme : the Medical and Welfare Network Chiba
Organisme : Yasuda Memorial Medical Foundation
Organisme : KAKENHI Grant-in-Aid for Scientific Research
ID : 20H03668
Organisme : KAKENHI Grant-in-Aid for Young Scientists
ID : 21K15963

Informations de copyright

© 2024 Wiley Periodicals LLC.

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Auteurs

Hiroshi Ohyama (H)

Department of Gastroenterology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Genome Analysis Center, Yamanashi Central Hospital, Yamanashi, Japan.
Department of Gastroenterology, Yamanashi Central Hospital, Yamanashi, Japan.

Yosuke Hirotsu (Y)

Genome Analysis Center, Yamanashi Central Hospital, Yamanashi, Japan.

Kenji Amemiya (K)

Genome Analysis Center, Yamanashi Central Hospital, Yamanashi, Japan.

Hiroyuki Amano (H)

Department of Gastroenterology, Yamanashi Central Hospital, Yamanashi, Japan.

Sumio Hirose (S)

Department of Gastroenterology, Yamanashi Central Hospital, Yamanashi, Japan.

Toshio Oyama (T)

Department of Pathology, Yamanashi Central Hospital, Yamanashi, Japan.

Yuji Iimuro (Y)

Department of Surgery, Yamanashi Central Hospital, Yamanashi, Japan.

Yuichiro Kojima (Y)

Department of Gastroenterology, Yamanashi Central Hospital, Yamanashi, Japan.

Rintaro Mikata (R)

Department of Gastroenterology, Graduate School of Medicine, Chiba University, Chiba, Japan.

Hitoshi Mochizuki (H)

Genome Analysis Center, Yamanashi Central Hospital, Yamanashi, Japan.
Department of Gastroenterology, Yamanashi Central Hospital, Yamanashi, Japan.

Naoya Kato (N)

Department of Gastroenterology, Graduate School of Medicine, Chiba University, Chiba, Japan.

Masao Omata (M)

Genome Analysis Center, Yamanashi Central Hospital, Yamanashi, Japan.
Department of Gastroenterology, Yamanashi Central Hospital, Yamanashi, Japan.
University of Tokyo, Tokyo, Japan.

Classifications MeSH