Evidence map›Paper›PMID 30811434›Full record

Trial reportPloS one2019

Detection of circulating tumor cells in drainage venous blood from colorectal cancer patients using a new filtration and cytology-based automated platform.

Masayuki Tsutsuyama, Hayao Nakanishi, Mayumi Yoshimura, Taihei Oshiro, Takashi Kinoshita, Koji Komori, Yasuhiro Shimizu, Yoshiyuki Ichinosawa, Seichin Kinuta, Kentaro Wajima and 4 more

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

16 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
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  4. Role of circulating tumor cells in breast cancer.Breast cancer (Tokyo, Japan) · 2025
    Review
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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 2 institutions in 1 country.

Masayuki TsutsuyamaDepartment of Gastroenterological Surgery, Aichi Cancer Center Central Hospital, Chikusa-ku, Nagoya, Japan.
Hayao NakanishiDepartment of Pathology and Molecular Diagnostics, Aichi Cancer Center Central Hospital, Chikusa-ku, Nagoya, Japan.ORCID 0000-0002-8885-9404
Mayumi YoshimuraDepartment of Pathology and Molecular Diagnostics, Aichi Cancer Center Central Hospital, Chikusa-ku, Nagoya, Japan.
Taihei OshiroDepartment of Gastroenterological Surgery, Aichi Cancer Center Central Hospital, Chikusa-ku, Nagoya, Japan.
Takashi KinoshitaDepartment of Gastroenterological Surgery, Aichi Cancer Center Central Hospital, Chikusa-ku, Nagoya, Japan.
Koji KomoriDepartment of Gastroenterological Surgery, Aichi Cancer Center Central Hospital, Chikusa-ku, Nagoya, Japan.ORCID 0000-0002-6834-995X
Yasuhiro ShimizuDepartment of Gastroenterological Surgery, Aichi Cancer Center Central Hospital, Chikusa-ku, Nagoya, Japan.
Yoshiyuki IchinosawaOptnics Precision Co. Ltd., Ashikaga, Tochigi, Japan.
Seichin KinutaOptnics Precision Co. Ltd., Ashikaga, Tochigi, Japan.
Kentaro WajimaMaruyasu Industries Co. Ltd., Okazaki, Aichi, Japan.
Yasufumi SakakibaraMaruyasu Industries Co. Ltd., Okazaki, Aichi, Japan.
Yasushi YatabeDepartment of Pathology and Molecular Diagnostics, Aichi Cancer Center Central Hospital, Chikusa-ku, Nagoya, Japan.
Seiji ItoDepartment of Gastroenterological Surgery, Aichi Cancer Center Central Hospital, Chikusa-ku, Nagoya, Japan.
Yasuhiro KoderaDepartment of Gastroenterological Surgery, Nagoya University Graduate School of Medicine, Showa-ku, Nagoya, Japan.
Aichi Cancer Center · JPNagoya University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Numerous technologies exist to detect circulating tumor cells (CTCs), although reports on cytological detection of CTCs remain limited. We recently developed a cytology-based CTC detection device using glass slides and light microscopy. In this study, we automated this previously manual device to improve its efficiency and cost effectiveness for clinical applications. We conducted a pilot study using this device to compare CTCs in peripheral blood (PB) and draining venous blood (DVB) from patients with colorectal cancer (CRC). The cytology-based automated CTC detection platform consisted of a disposable filtration device with a three-dimensional (3D) metal filter and multichannel automated CTC enrichment device. This platform allowed rapid and gentle filtration of CTCs and their efficient transfer from the filter to glass slides for subsequent Papanicolaou (Pap) and immunocytochemical (ICC) staining. Cytological diagnosis of CTCs was performed by observing permanent glass slide specimens by light microscopy. The current pilot clinical study enrolled CRC patients (n = 26) with stage I-IV tumors, who underwent surgery. PB was collected before surgery, and DVB was obtained from the mesenteric vein immediately after resection. Based on the CTC morphology obtained from PB and DVB samples, we proposed the following cytological criteria for the diagnosis of CTCs: pan-cytokeratin-positive, atypical cells with malignant morphological features identified by Pap staining. The numbers of CTCs defined by these criteria were significantly higher in DVB than PB from CRC patients (p<0.01), and the number of CTCs in DVB was increased significantly with stage progression (p<0.05). These results suggest that DVB may be another potential source of CTCs other than PB for liquid biopsies including downstream analysis. This automated cytology-based CTC detection device therefore provides a unique and powerful tool to investigate the significance of CTCs in CRC patients in a clinical setting.

Indexed as

AutomationCell SeparationColorectal NeoplasmsMicroscopyNeoplastic Cells, CirculatingAdultAgedAged, 80 and overBiomarkers, TumorFemaleFiltrationHumansMaleMiddle AgedPilot ProjectsBiomarkers, Tumor

Identifiers

PMID30811434
PMCPMC6392262
OpenAlexW2917918011

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.