Evidence map›Paper›PMID 32194728›Full record

ArticleOncology letters2020

Using the polymeric circulating tumor cell chip to capture circulating tumor cells in blood samples of patients with colorectal cancer.

Kazumasa Kure, Masaki Hosoya, Takae Ueyama, Midori Fukaya, Kiichi Sugimoto, Yuichi Tomiki, Takashi Ohnaga, Kazuhiro Sakamoto, Hiromitsu Komiyama

Open access · diamondAbstract read
In one paragraph

Article in Oncology letters, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.7field-weighted citation impact, top 29% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

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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

9 authors at 2 institutions in 1 country.

Kazumasa KureDepartment of Coloproctological Surgery, Juntendo University School of Medicine, Tokyo 113-8421, Japan.
Masaki HosoyaDepartment of Coloproctological Surgery, Juntendo University School of Medicine, Tokyo 113-8421, Japan.
Takae UeyamaDepartment of Coloproctological Surgery, Juntendo University School of Medicine, Tokyo 113-8421, Japan.
Midori FukayaDepartment of Coloproctological Surgery, Juntendo University School of Medicine, Tokyo 113-8421, Japan.
Kiichi SugimotoDepartment of Coloproctological Surgery, Juntendo University School of Medicine, Tokyo 113-8421, Japan.
Yuichi TomikiDepartment of Coloproctological Surgery, Juntendo University School of Medicine, Tokyo 113-8421, Japan.
Takashi OhnagaCentral Research Laboratories, Toyama Industrial Technology Center, Toyama 933-0981, Japan.
Kazuhiro SakamotoDepartment of Coloproctological Surgery, Juntendo University School of Medicine, Tokyo 113-8421, Japan.
Hiromitsu KomiyamaDepartment of Coloproctological Surgery, Juntendo University School of Medicine, Tokyo 113-8421, Japan.
Juntendo University · JPToyama Industrial Technology Center · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The current study clarified the accuracy of a circulating tumor cell (CTC) detection system to diagnose colorectal cancer using blood samples. The system uses the 'polymeric CTC-chip,' (CTC-chip), which is a microfluidic device that is used for CTC isolation. CTCs are considered sensitive diagnostic biomarkers. However, their concentration in the peripheral blood is low and requires highly sensitive and specific capturing techniques. The capture efficiency of the polymeric CTC-chip was first assessed using cell suspensions of the colorectal cancer cell line HCT-116, which was reported as 90.9% in a phosphate-buffered saline suspension and 65.0% in the blood. The CTC-chip was then used to detect CTCs in blood samples obtained from 13 patients with stage II-IV colorectal cancer. On average, the CTCs/ml was lower in patients with stages II and III colorectal cancer (3.3±2.3) than in those with stage IV (7.0±6.2). In patients with stages II-IV, 92% had ≥1 CTC per ml, which was significantly higher than the positive rate (15%) detected using the carbohydrate antigen 19-9 test (CA19-9). Furthermore, CTCs were detected in all patients with stage II and III colorectal cancer, including a number of patients with negative results for the carcinoembryonic antigen (CEA) and CA19-9 tests. With the polymeric CTC-chip detection system, CTCs can be effective cancer markers, particularly for patients with stage II and III colorectal cancer who often exhibit negative conventional serum marker test results. The CTC-chip system may also facilitate the detection of cancer progression based on CTC concentration.

Indexed as

cancer screeningcirculating tumor cellscolorectal cancermicrofluidic devicestumor biomarkers

Identifiers

PMID32194728
PMCPMC7041365
OpenAlexW3002857274

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.