Evidence map›Paper›PMID 38385113›Full record

ArticleOncology letters2024

Next‑generation sequencing to identify genetic mutations in pancreatic cancer using intraoperative peritoneal washing fluid.

Yutaka Nakano, Gaku Shimane, Kohei Nakamura, Reika Takamatsu, Eriko Aimono, Hiroshi Yagi, Yuta Abe, Yasushi Hasegawa, Shutaro Hori, Masayuki Tanaka and 4 more

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.8field-weighted citation impact, top 25% of its field
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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. 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 at 1 institution in 1 country.

Yutaka NakanoDepartment of Surgery, Keio University School of Medicine, Tokyo 160-8582, Japan.
Gaku ShimaneDepartment of Surgery, Keio University School of Medicine, Tokyo 160-8582, Japan.
Kohei NakamuraGenomics Unit, Keio University School of Medicine, Tokyo 160-8582, Japan.
Reika TakamatsuGenomics Unit, Keio University School of Medicine, Tokyo 160-8582, Japan.
Eriko AimonoGenomics Unit, Keio University School of Medicine, Tokyo 160-8582, Japan.
Hiroshi YagiDepartment of Surgery, Keio University School of Medicine, Tokyo 160-8582, Japan.
Yuta AbeDepartment of Surgery, Keio University School of Medicine, Tokyo 160-8582, Japan.
Yasushi HasegawaDepartment of Surgery, Keio University School of Medicine, Tokyo 160-8582, Japan.
Shutaro HoriDepartment of Surgery, Keio University School of Medicine, Tokyo 160-8582, Japan.
Masayuki TanakaDepartment of Surgery, Keio University School of Medicine, Tokyo 160-8582, Japan.
Yohei MasugiDepartment of Pathology, Keio University School of Medicine, Tokyo 160-8582, Japan.
Minoru KitagoDepartment of Surgery, Keio University School of Medicine, Tokyo 160-8582, Japan.
Hiroshi NishiharaGenomics Unit, Keio University School of Medicine, Tokyo 160-8582, Japan.
Yuko KitagawaDepartment of Surgery, Keio University School of Medicine, Tokyo 160-8582, Japan.
Keio University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The efficacy of next-generation sequencing (NGS) of tumor-derived DNA from intraoperative peritoneal washing fluid (IPWF) of patients with pancreatic ductal adenocarcinoma (PDAC) who intend to undergo curative resection remains unclear. The aim of the present study was to evaluate whether genomic mutations in tumor-derived DNA from IPWF samples of patients with PDAC who intend to undergo curative resection could be detected using NGS. A total of 12 such patients were included in this study. Cytology of IPWF (CY) was assessed and NGS of genomic tumor-derived DNA from the IPWF was performed to determine whether genomic mutations could be detected in these patient samples. A total of 2 patients (16.7%) had a CY(+) status and 1 patient (8.3%) showed intraoperative macro-peritoneal dissemination; 11 patients underwent radical surgery. Actionable gene alterations were detected in 8 (80.0%) out of the 10 patients with CY(-) status based on NGS of IPWF samples, and 3 (37.5%) patients among those with actionable gene mutations identified from IPWF samples underwent peritoneal dissemination after surgery within ~12 months. The most common genomic mutation was in

Indexed as

cytologyIPWFNGSpancreatic cancertumor-derived DNA

Identifiers

PMID38385113
PMCPMC10877230
OpenAlexW4391474397

What OpenQuestion holds

Textmetadata
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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.