Evidence map›Paper›PMID 31553731›Full record

ArticlePloS one2019

Detection and prognostic relevance of circulating tumour cells (CTCs) in Asian breast cancers using a label-free microfluidic platform.

Yoon-Sim Yap, Man Chun Leong, Yong Wei Chua, Kiley Wei Jen Loh, Guek Eng Lee, Elaine Hsuen Lim, Rebecca Dent, Raymond Chee Hui Ng, John Heng-Chi Lim, Garima Singh and 6 more

Abstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Review
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  4. Use and application of organ-on-a-chip platforms in cancer research.Journal of cell communication and signaling · 2023
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  11. Hexokinase 2 discerns a novel circulating tumor cell population associated with poor prognosis in lung cancer patients.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
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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

16 authors.

Yoon-Sim YapDivision of Medical Oncology, National Cancer Centre Singapore, Singapore.ORCID 0000-0002-0347-5066
Man Chun LeongBiolidics Ltd, Singapore.
Yong Wei ChuaDepartment of Pathology, Singapore General Hospital, Singapore.
Kiley Wei Jen LohDivision of Medical Oncology, National Cancer Centre Singapore, Singapore.
Guek Eng LeeDivision of Medical Oncology, National Cancer Centre Singapore, Singapore.
Elaine Hsuen LimDivision of Medical Oncology, National Cancer Centre Singapore, Singapore.
Rebecca DentDivision of Medical Oncology, National Cancer Centre Singapore, Singapore.
Raymond Chee Hui NgDivision of Medical Oncology, National Cancer Centre Singapore, Singapore.
John Heng-Chi LimClinical Trials and Epidemiology Office, National Cancer Centre Singapore, Singapore.
Garima SinghBiolidics Ltd, Singapore.
Angela TanBiolidics Ltd, Singapore.
Guofeng GuanBiolidics Ltd, Singapore.
Andrew WuBiolidics Ltd, Singapore.
Yi Fang LeeBiolidics Ltd, Singapore.
Ali Asgar S BhagatBiolidics Ltd, Singapore.ORCID 0000-0002-4695-8762
Darren Wan-Teck LimDivision of Medical Oncology, National Cancer Centre Singapore, Singapore.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesWe aimed to study the prevalence of CTCs in breast cancer (BC) patients undergoing neoadjuvant or palliative therapy with a label-free microfluidic platform (ClearCell FX), and its prognostic relevance in metastatic BC (mBC). MATERIALS AND

methodsPeripheral blood samples were collected from 108 BC patients before starting a new line of treatment ("baseline"), majority of whom had mBC (76/108; 70.4%). CTCs were retrieved by dean flow fractionation that enriched for larger cells, and enumerated using immunofluorescence-based staining. Progression-free survival (PFS) in mBC patients was analysed using Kaplan-Meier method; cox proportional hazard models were used for univariable and multivariable analyses.

resultsThe detection rate of CTCs before starting a new line of treatment was 75.9% (n = 108; median: 8 CTCs/7.5 ml blood) at a cut off of ≥2 CTCs. PFS was inferior for mBC patients with baseline CTC count ≥5 CTCs/7.5 ml blood vs. those with < 5 CTCs/7.5 ml blood (median PFS: 4.3 vs. 7.0 months; p-value: 0.037). The prognostic relevance of CTCs was most significant in patients with HER2- mBC (median PFS: 4.1 vs. 8.3 months; p-value: 0.032), luminal (HR+HER2-) subtype (median PFS: 4.2 vs. 8.3 months; p-value: 0.048), and patients who had one or more prior treatments (median PFS: 4.2 vs. 7.0 months; p-value: 0.02). On multivariable analysis, baseline CTC level (hazard ratio (HR): 1.84, p-value: 0.02) and pre-treatment status (HR: 1.87, p-value: 0.05) were independent predictors of PFS.

conclusionsThis work demonstrates the prognostic significance of CTCs in mBC detected using a label-free size-based enrichment platform.

Indexed as

AdultAgedAsian PeopleBreast NeoplasmsCell CountErb-b2 Receptor Tyrosine KinasesFemaleHumansImmunohistochemistryKaplan-Meier EstimateMicrofluidicsMiddle AgedNeoplastic Cells, CirculatingPrognosisProgression-Free SurvivalProspective StudiesERBB2 protein, humanErb-b2 Receptor Tyrosine Kinases

Identifiers

PMID31553731
PMCPMC6760773

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LicenceCC BY
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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.