Evidence map›Paper›PMID 34987518›Full record

Trial reportFrontiers in immunology2021

The Tumor Immune Landscape and Architecture of Tertiary Lymphoid Structures in Urothelial Cancer.

Nick van Dijk, Alberto Gil-Jimenez, Karina Silina, Maurits L van Montfoort, Sarah Einerhand, Lars Jonkman, Charlotte S Voskuilen, Dennis Peters, Joyce Sanders, Yoni Lubeck and 7 more

Open access · goldAbstract readClinical Trial
In one paragraph

Trial report in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
6.3field-weighted citation impact, top 3% 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

26 citing papers in PubMed, 39 citations in OpenAlex.

  1. Review
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  16. Tertiary lymphoid structures and their therapeutic implications in cancer.Cellular oncology (Dordrecht, Netherlands) · 2024
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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

17 authors at 4 institutions in 3 countries.

Nick van DijkDepartment of Medical Oncology, The Netherlands Cancer Institute, Amsterdam, Netherlands.
Alberto Gil-JimenezDepartment of Molecular Carcinogenesis, The Netherlands Cancer Institute, Amsterdam, Netherlands.
Karina SilinaInstitute of Experimental Immunology, University of Zurich, Zurich, Switzerland.
Maurits L van MontfoortDepartment of Pathology, The Netherlands Cancer Institute, Amsterdam, Netherlands.
Sarah EinerhandDepartment of Medical Oncology, The Netherlands Cancer Institute, Amsterdam, Netherlands.
Lars JonkmanDepartment of Medical Oncology, Maastricht University Medical Center, Maastricht, Netherlands.
Charlotte S VoskuilenDepartment of Medical Oncology, The Netherlands Cancer Institute, Amsterdam, Netherlands.
Dennis PetersCore Facility Molecular Pathology & Biobanking, The Netherlands Cancer Institute, Amsterdam, Netherlands.
Joyce SandersDepartment of Pathology, The Netherlands Cancer Institute, Amsterdam, Netherlands.
Yoni LubeckDepartment of Pathology, The Netherlands Cancer Institute, Amsterdam, Netherlands.
Annegien BroeksCore Facility Molecular Pathology & Biobanking, The Netherlands Cancer Institute, Amsterdam, Netherlands.
Erik HooijbergDepartment of Pathology, The Netherlands Cancer Institute, Amsterdam, Netherlands.
Daniel J VisDepartment of Molecular Carcinogenesis, The Netherlands Cancer Institute, Amsterdam, Netherlands.
Maries van den BroekInstitute of Experimental Immunology, University of Zurich, Zurich, Switzerland.
Lodewyk F A WesselsDepartment of Molecular Carcinogenesis, The Netherlands Cancer Institute, Amsterdam, Netherlands.
Bas W G van RhijnDepartment of Urology, The Netherlands Cancer Institute, Amsterdam, Netherlands.
Michiel S van der HeijdenDepartment of Medical Oncology, The Netherlands Cancer Institute, Amsterdam, Netherlands.
The Netherlands Cancer Institute · NLOncode Institute · NLUniversity of Zurich · CHMaastricht University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Candidate immune biomarkers have been proposed for predicting response to immunotherapy in urothelial cancer (UC). Yet, these biomarkers are imperfect and lack predictive power. A comprehensive overview of the tumor immune contexture, including Tertiary Lymphoid structures (TLS), is needed to better understand the immunotherapy response in UC. We analyzed tumor sections by quantitative multiplex immunofluorescence to characterize immune cell subsets in various tumor compartments in tumors without pretreatment and tumors exposed to preoperative anti-PD1/CTLA-4 checkpoint inhibitors (NABUCCO trial). Pronounced immune cell presence was found in UC invasive margins compared to tumor and stroma regions. CD8

Indexed as

AgedCD8-Positive T-LymphocytesCell DifferentiationCells, CulturedCTLA-4 AntigenFemaleFluorescent Antibody TechniqueForkhead Transcription FactorsHumansImmune Checkpoint InhibitorsImmunotherapyIpilimumabLymphocyte ActivationMaleMiddle AgedNivolumabCTLA-4 AntigenForkhead Transcription FactorsFOXP3 protein, humanImmune Checkpoint InhibitorsIpilimumabNivolumabPDCD1 protein, humanProgrammed Cell Death 1 Receptorbladder cancerimmunotherapymultiplex immunofluorescencetertiary lymphoid structures (TLS)tumor microenvironmenturothelial cancer

Identifiers

PMID34987518
PMCPMC8721669
OpenAlexW4200371667

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.