Evidence map›Paper›PMID 32064107›Full record

ArticleMolecular and clinical oncology2020

Detection of circulating tumor cells in patients with lung cancer using metallic micro-cavity array filter: A pilot study.

Hideo Ichimura, Takeshi Nawa, Yusuke Yamamoto, Kei Shimizu, Keisuke Kobayashi, Shinsuke Kitazawa, Hisashige Kanbara, Taihei Odagiri, Katsuya Endo, Tatsuya Matsunaga and 3 more

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Article in Molecular and clinical oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

6 citing papers in PubMed, 9 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

13 authors at 3 institutions in 1 country.

Hideo IchimuraDepartment of Thoracic Surgery, Hitachi General Hospital, Hitachi, Ibaraki 317-0077, Japan.
Takeshi NawaDepartment of Respiratory Medicine, Hitachi General Hospital, Hitachi, Ibaraki 317-0077, Japan.
Yusuke YamamotoDepartment of Respiratory Medicine, Hitachi General Hospital, Hitachi, Ibaraki 317-0077, Japan.
Kei ShimizuDepartment of Respiratory Medicine, Hitachi General Hospital, Hitachi, Ibaraki 317-0077, Japan.
Keisuke KobayashiDepartment of Thoracic Surgery, Hitachi General Hospital, Hitachi, Ibaraki 317-0077, Japan.
Shinsuke KitazawaDepartment of Thoracic Surgery, Hitachi General Hospital, Hitachi, Ibaraki 317-0077, Japan.
Hisashige KanbaraLife Science Business Headquaters, Hitachi Chemical Co., Ltd., Chikusei, Ibaraki 308-0861, Japan.
Taihei OdagiriLife Science Business Headquaters, Hitachi Chemical Co., Ltd., Chikusei, Ibaraki 308-0861, Japan.
Katsuya EndoLife Science Business Headquaters, Hitachi Chemical Co., Ltd., Chikusei, Ibaraki 308-0861, Japan.
Tatsuya MatsunagaLife Science Business Headquaters, Hitachi Chemical Co., Ltd., Chikusei, Ibaraki 308-0861, Japan.
Seita NakamuraLife Science Business Headquaters, Hitachi Chemical Co., Ltd., Chikusei, Ibaraki 308-0861, Japan.
Satomi YagiLife Science Business Headquaters, Hitachi Chemical Co., Ltd., Chikusei, Ibaraki 308-0861, Japan.
Yukio SatoDepartment of Thoracic Surgery, University of Tsukuba, Tsukuba, Ibaraki 305-8575, Japan.
Hitachi General Hospital · JPHitachi (Japan) · JPUniversity of Tsukuba · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We have developed a metallic micro-cavity array filter and an automated detection system for capturing circulating tumor cells (CTCs). In this single institutional pilot study, we assessed the ability of this device to detect CTCs in patients with lung cancer at each stage. Patients diagnosed with lung cancer, undergoing planned surgery for lung cancer, or suspected of having lung cancer were recruited (40 recruited and 2 excluded). Blood samples were obtained from the patients and 3 ml whole blood was applied to the device without any preparation. The captured cells were stained to differentiate the nucleus, and determine cytokeratin and CD45 expression. Subsequently, two operators blinded to clinical information counted the number of CTCs. Sample collection was performed at the time of recruitment, before treatment and ~3 months after initial blood collection. CTC counts at recruitment were 1.4±0.4, 1.8±1.2, 1.3±0.6 and 7.4±5.1 (mean ± SE) in clinical stages I, II, III and IV, respectively. No significant difference was observed among the stages. These data indicated the ability of this device to detect CTCs at early or non-metastatic stages of lung cancer. Further research on a larger scale is needed for a more accurate assessment of the device, and research on the utility of captured cells remains a future challenge.

Indexed as

circulating tumor cellclinical stagelung cancermicro-cavity array filter

Identifiers

PMID32064107
PMCPMC7016515
OpenAlexW2999463847

What OpenQuestion holds

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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.