Evidence map›Paper›PMID 40395448›Full record

ArticleEndoscopy international open2025

Benefits of macroscopic on-site evaluation in endoscopic ultrasound-guided tissue acquisition for comprehensive genomic profiling.

Junya Sato, Hirotoshi Ishiwatari, Kazuma Ishikawa, Hiroki Sakamoto, Takuya Doi, Masahiro Yamamura, Kazunori Takada, Yoichi Yamamoto, Masao Yoshida, Sayo Ito and 4 more

Abstract read
In one paragraph

Article in Endoscopy international open, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Junya SatoDivision of Endoscopy, Shizuoka Cancer Center, Sunto-gun, Japan.ORCID 0000-0003-0514-4452
Hirotoshi IshiwatariDivision of Endoscopy, Shizuoka Cancer Center, Sunto-gun, Japan.ORCID 0000-0002-6719-4466
Kazuma IshikawaDepartment of Medical Oncology, Sapporo Medical University, Sapporo, Japan.
Hiroki SakamotoDivision of Endoscopy, Shizuoka Cancer Center, Sunto-gun, Japan.
Takuya DoiDivision of Endoscopy, Shizuoka Cancer Center, Sunto-gun, Japan.ORCID 0009-0009-7202-0178
Masahiro YamamuraDivision of Endoscopy, Shizuoka Cancer Center, Sunto-gun, Japan.
Kazunori TakadaDivision of Endoscopy, Shizuoka Cancer Center, Sunto-gun, Japan.
Yoichi YamamotoDivision of Endoscopy, Shizuoka Cancer Center, Sunto-gun, Japan.
Masao YoshidaDivision of Endoscopy, Shizuoka Cancer Center, Sunto-gun, Japan.ORCID 0000-0001-7272-0187
Sayo ItoDivision of Endoscopy, Shizuoka Cancer Center, Sunto-gun, Japan.ORCID 0000-0003-0916-5445
Noboru KawataDivision of Endoscopy, Shizuoka Cancer Center, Sunto-gun, Japan.
Kenichiro ImaiDivision of Endoscopy, Shizuoka Cancer Center, Sunto-gun, Japan.
Kinichi HottaDivision of Endoscopy, Shizuoka Cancer Center, Sunto-gun, Japan.
Hiroyuki OnoDivision of Endoscopy, Shizuoka Cancer Center, Sunto-gun, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and study aims: Matched therapy based on comprehensive genomic profiling is a potential treatment option for patients with inoperable pancreatic cancer; however, the optimal method for obtaining tissue samples suitable for comprehensive genomic profiling using endoscopic ultrasound-guided tissue acquisition remains unclear. This study aimed to determine the optimal endoscopic ultrasound-guided tissue acquisition method to obtain samples for comprehensive genomic profiling. Patients and methods: This retrospective study included 86 consecutive patients with pancreatic cancer who underwent comprehensive genomic profiling using FoundationOne CDx (Foundation Medicine Inc.) and endoscopic ultrasound-guided tissue acquisition between June 2019 and January 2023. Macroscopic visible core length was measured using on-site macroscopic evaluation in all patients. Foundation Medicine Inc. reported analysis results categorized as passed (successful FoundationOne CDx), qualified, or failed. We investigated factors predicting successful FoundationOne CDx treatment. Results: Needles sized 22, 20, and 19 gauge were used in 63, one, and 23 patients, respectively. The stylet slow-pull and suction techniques were performed in 43 and 41 patients, respectively. Median total macroscopic visible core length in the formalin-fixed paraffin-embedded blocks subjected to FoundationOne CDx was 41 mm. The success rate for FoundationOne CDx was 66%. Multiple linear regression analysis revealed that macroscopic visible core length independently affected successful FoundationOne CDx ( Conclusions: In tissue specimens obtained using endoscopic ultrasound-guided tissue acquisition, macroscopic visible core length can be associated with an appropriate sample for FoundationOne CDx.

Indexed as

Endoscopic ultrasonographyPancreasTissue diagnosis

Identifiers

PMID40395448
PMCPMC12090978

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.