Evidence map›Paper›PMID 26923772›Full record

ArticleBMC cancer2016

Vimentin and Ki67 expression in circulating tumour cells derived from castrate-resistant prostate cancer.

C R Lindsay, S Le Moulec, F Billiot, Y Loriot, M Ngo-Camus, P Vielh, K Fizazi, C Massard, F Farace

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in BMC cancer, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01786031 (Prostate Cancer Evaluation of TaRgets in Genito Urinary Screening Program), which is not on this map. Cited by 53 papers.

0numbers the graph read from it
0cells of the map it votes in
53citing papers in PubMed
6.3field-weighted citation impact, top 2% 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.

NCT01786031 nacompletednot on this map

Prostate Cancer Evaluation of TaRgets in Genito Urinary Screening Program

TypeinterventionalSponsorGustave Roussy, Cancer Campus, Grand ParisRan2012 to 2015Enrolled55ConditionsMetastatic Castration Resistant Prostate Cancer PatientsArmsmetastasis biopsy
3 · Its place in the literature

Who cites it

53 citing papers in PubMed, 98 citations in OpenAlex.

  1. Trial
  2. The effect of aspirin on circulating tumor cells in metastatic colorectal and breast cancer patients: a phase II trial study.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2018
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  10. MKI67 with arterial hypertension predict a poor survival for prostate cancer patients, a real-life investigation.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2024
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  20. Can we use Ki67 expression to predict prostate cancer aggressiveness?Revista do Colegio Brasileiro de Cirurgioes · 2022
    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

9 authors at 4 institutions in 1 country.

C R LindsayINSERM U981, University of Paris-Sud XI, Translational Research Laboratory, Gustave Roussy Cancer Campus, Villejuif, France. colin.lindsay@gustaveroussy.fr.
S Le MoulecDepartment of Medical Oncology, Bergonie Cancer Institute, Bordeaux, France. sylvestre.lemoulec@gmail.com.
F BilliotINSERM U981, University of Paris-Sud XI, Translational Research Laboratory, Gustave Roussy Cancer Campus, Villejuif, France. fanny.billiot@gustaveroussy.fr.
Y LoriotDepartment of Medical Oncology, Gustave Roussy Cancer Campus, Villejuif, France. yohann.loriot@gustaveroussy.fr.
M Ngo-CamusDepartment of Medical Oncology, Gustave Roussy Cancer Campus, Villejuif, France. maud.ngocamus@gustaveroussy.fr.
P VielhINSERM U981, University of Paris-Sud XI, Translational Research Laboratory, Gustave Roussy Cancer Campus, Villejuif, France. philippe.vielh@gustaveroussy.fr.
K FizaziDepartment of Medical Oncology, Gustave Roussy Cancer Campus, Villejuif, France. karim.fizazi@gustaveroussy.fr.
C MassardDepartment of Medical Oncology, Gustave Roussy Cancer Campus, Villejuif, France. christophe.massard@gustaveroussy.fr.
F FaraceINSERM U981, University of Paris-Sud XI, Translational Research Laboratory, Gustave Roussy Cancer Campus, Villejuif, France. francoise.farace@gustaveroussy.fr.
Institut Gustave Roussy · FRInserm · FRInstitut Bergonié · FRUniversité Paris-Sud · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHigh circulating tumor cell (CTC) counts are associated with poor prognosis in advanced prostate cancer, and recently CTC number was suggested to be a surrogate for survival in metastatic castrate-resistant prostate cancer (mCRPC). Ki67 and vimentin are well-characterised markers of tumour cell proliferation and the epithelial-mesenchymal transition (EMT), respectively. Here we asked if the expression of vimentin and Ki67 in CTCs offered prognostic or predictive information in mCRPC.

methodsIn two separate patient cohorts, anti-vimentin or anti-Ki67 antibodies were added to the free channel in the CellSearch® system for analysis of peripheral blood samples. For each cohort, association of CTC number with clinical characteristics were assessed using Fisher's exact, Mann-Whitney and chi-squared tests. Kaplan-Meier method and log-rank tests were used to analyse overall survival (OS) of vimentin-expressing and Ki67-expressing CTC patient cohorts.

resultsIn this retrospective analysis, CTC vimentin expression was analysed in 142 blood samples from 93 patients, and CTC Ki67 expression was analysed in 90 blood samples from 51 patients. In the vimentin cohort, 80/93 (86 %) of baseline samples from patients were CTC-positive overall (≥1 total CTC per 7.5 mls blood), and 30/93 (32.3 %) vimentin CTC-positive (≥1 vimentin-positive CTC per 7.5 mls blood). 41/51 (80.4 %) of baseline samples from patients in the Ki67 cohort were CTC-positive overall, and 23/51 (45.1 %) Ki67 CTC-positive (≥1 Ki67-positive CTC per 7.5 mls blood). There was no significant difference in baseline PSA in patients with vimentin-positive CTC at baseline versus those with no vimentin-positive CTC at baseline (p = 0.33). A significant reduction in OS was shown in patients with vimentin-positive CTC compared to those without vimentin-positive CTC (median 305 days vs 453 days, p = 0.0293). There was no significant difference in baseline PSA in patients with Ki67-positive CTC at baseline versus those without Ki67-positive CTC (p = 0.228), but OS was significantly reduced in the Ki67-positive CTC group (median 512 days vs 751 days, p = 0.0091). No changes in relative proportion of vimentin- or Ki67-positive CTCs were observed in post-treatment samples compared to baseline.

conclusionsAnalysis of vimentin and Ki67 expression can straightforwardly be assessed in CTCs from patients with mCRPC. Poorer survival outcomes were observed in vimentin- and Ki67-positive CTC patients. TRANSLATIONAL STUDY PROTOCOLS: CEC-CTC (IDRCB2008-AOO585-50) and Petrus ( NCT01786031 ).

Indexed as

Biomarkers, TumorAgedAged, 80 and overCombined Modality TherapyGene ExpressionHumansImmunophenotypingKi-67 AntigenMaleMiddle AgedNeoplasm MetastasisNeoplasm StagingNeoplastic Cells, CirculatingPrognosisProstatic Neoplasms, Castration-ResistantReproducibility of ResultsBiomarkers, TumorKi-67 AntigenVimentin

Identifiers

PMID26923772
PMCPMC4770547
OpenAlexW2289256168

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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.