Evidence map›Paper›PMID 36189320›Full record

ArticleFrontiers in immunology2022

CyTOF analysis identifies unusual immune cells in urine of BCG-treated bladder cancer patients.

Eva Castellano, Célia Samba, Gloria Esteso, Laura Simpson, Elena Vendrame, Eva M García-Cuesta, Sheila López-Cobo, Mario Álvarez-Maestro, Ana Linares, Asier Leibar and 5 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.6field-weighted citation impact, top 10% 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

13 citing papers in PubMed, 13 citations in OpenAlex.

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  11. Intratumoral PD1Cells · 2023
    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

15 authors at 4 institutions in 2 countries.

Eva CastellanoDepartment of Immunology and Oncology, National Centre for Biotechnology (CNB) Spanish National Research Council (CSIC), Madrid, Spain.
Célia SambaDepartment of Immunology and Oncology, National Centre for Biotechnology (CNB) Spanish National Research Council (CSIC), Madrid, Spain.
Gloria EstesoDepartment of Immunology and Oncology, National Centre for Biotechnology (CNB) Spanish National Research Council (CSIC), Madrid, Spain.
Laura SimpsonDepartment of Medicine, Stanford University School of Medicine, Stanford, CA, United States.
Elena VendrameDepartment of Medicine, Stanford University School of Medicine, Stanford, CA, United States.
Eva M García-CuestaDepartment of Immunology and Oncology, National Centre for Biotechnology (CNB) Spanish National Research Council (CSIC), Madrid, Spain.
Sheila López-CoboDepartment of Immunology and Oncology, National Centre for Biotechnology (CNB) Spanish National Research Council (CSIC), Madrid, Spain.
Mario Álvarez-MaestroUrology Department, La Paz University Hospital Institute for Health Research (IdiPAZ), Madrid, Spain.
Ana LinaresUrology Unit, Infanta Sofia Hospital, Madrid, Spain.
Asier LeibarUrology Unit, Infanta Sofia Hospital, Madrid, Spain.
Thanmayi RanganathDepartment of Medicine, Stanford University School of Medicine, Stanford, CA, United States.
Hugh T ReyburnDepartment of Immunology and Oncology, National Centre for Biotechnology (CNB) Spanish National Research Council (CSIC), Madrid, Spain.
Luis Martínez-PiñeiroUrology Department, La Paz University Hospital Institute for Health Research (IdiPAZ), Madrid, Spain.
Catherine BlishDepartment of Medicine, Stanford University School of Medicine, Stanford, CA, United States.
Mar Valés-GómezDepartment of Immunology and Oncology, National Centre for Biotechnology (CNB) Spanish National Research Council (CSIC), Madrid, Spain.
Stanford University · USHospital Universitario Infanta Sofía · ESCentro Nacional de Biotecnología · ESConsejo Superior de Investigaciones Científicas · ES

Funding

Modeling the influence of sex on natural killer cell networksDP2AI112193 · NIAID · STANFORD UNIVERSITY · PI BLISH, CATHERINE A · 2013 to 2015
$2.5M
NIAID NIH HHS DP2 AI112193
6 · The paper itself

Abstract

High grade non-muscle-invasive bladder tumours are treated with transurethral resection followed by recurrent intravesical instillations of Bacillus Calmette Guérin (BCG). Although most bladder cancer patients respond well to BCG, there is no clinical parameter predictive of treatment response, and when treatment fails, the prognosis is very poor. Further, a high percentage of NMIBC patients treated with BCG suffer unwanted effects that force them to stop treatment. Thus, early identification of patients in which BCG treatment will fail is really important. Here, to identify early stage non-invasive biomarkers of non-responder patients and patients at risk of abandoning the treatment, we longitudinally analysed the phenotype of cells released into the urine of bladder cancer patients 3-7 days after BCG instillations. Mass cytometry (CyTOF) analyses revealed a large proportion of granulocytes and monocytes, mostly expressing activation markers. A novel population of CD15

Indexed as

Urinary Bladder NeoplasmsAdministration, IntravesicalBCG VaccineHumansPilot ProjectsPrognosisBCG VaccineBCG - Bacille Calmette-Guérin vaccinebladder cancergranulocytesimmune responseleukocytesmass cytometry (CyTOF)urine cells

Identifiers

PMID36189320
PMCPMC9520259
OpenAlexW4295928750

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.