Evidence map›Paper›PMID 33827905›Full record

ArticleJournal for immunotherapy of cancer2021

Intratumoral CD103+ CD8+ T cells predict response to PD-L1 blockade.

Romain Banchereau, Avantika S Chitre, Alexis Scherl, Thomas D Wu, Namrata S Patil, Patricia de Almeida, Edward E Kadel Iii, Shravan Madireddi, Amelia Au-Yeung, Chikara Takahashi and 20 more

Open access · goldAbstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 108 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
108citing papers in PubMed, 1 pooled it
9.6field-weighted citation impact, top 1% 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

108 citing papers in PubMed, 1 synthesis or guideline pooled it, 144 citations in OpenAlex.

  1. Pooled it
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  13. Tissue-resident memory T cells reshapeFrontiers in immunology · 2026
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48 more citing papers are in PubMed but not listed here.

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

30 authors at 4 institutions in 2 countries.

Romain Banchereau *Department of Oncology Biomarker Development, Genentech Inc, South San Francisco, California, USA.
Avantika S Chitre *Department of Cancer Immunology, Genentech Inc, South San Francisco, California, USA.
Alexis Scherl *Department of Research Pathology, Genentech Inc, South San Francisco, California, USA.
Thomas D Wu *Department of Bioinformatics and Computational Biology, Genentech Inc, South San Francisco, California, USA.
Namrata S Patil *Department of Oncology Biomarker Development, Genentech Inc, South San Francisco, California, USA.
Patricia de AlmeidaDepartment of Cancer Immunology, Genentech Inc, South San Francisco, California, USA.
Edward E Kadel IiiDepartment of Oncology Biomarker Development, Genentech Inc, South San Francisco, California, USA.
Shravan MadireddiDepartment of Cancer Immunology, Genentech Inc, South San Francisco, California, USA.
Amelia Au-YeungDepartment of OMNI Biomarker Development, Genentech Inc, South San Francisco, California, USA.
Chikara TakahashiDepartment of OMNI Biomarker Development, Genentech Inc, South San Francisco, California, USA.
Ying-Jiun ChenDepartment of Microchemistry, Proteomics, Lipidomics, and Next Generation Sequencing, Genentech Inc, South San Francisco, California, USA.
Zora ModrusanDepartment of Microchemistry, Proteomics, Lipidomics, and Next Generation Sequencing, Genentech Inc, South San Francisco, California, USA.
Jacqueline McBrideDepartment of OMNI Biomarker Development, Genentech Inc, South San Francisco, California, USA.
Rhea NersesianDepartment of Oncology Biomarker Development, Genentech Inc, South San Francisco, California, USA.
Ehab A El-GabryVentana Medical Systems Inc, Tucson, Arizona, USA.
Mark D RobidaVentana Medical Systems Inc, Tucson, Arizona, USA.
Jeffrey C HungDepartment of Research Pathology, Genentech Inc, South San Francisco, California, USA.
Marcin KowanetzDepartment of Oncology Biomarker Development, Genentech Inc, South San Francisco, California, USA.
Wei ZouDepartment of Biostatistics Oncology, Genentech Inc, South San Francisco, California, USA.
Mark McClelandDepartment of Oncology Biomarker Development, Genentech Inc, South San Francisco, California, USA.
Patrick CaplaziDepartment of Research Pathology, Genentech Inc, South San Francisco, California, USA.
Shadi Toghi EshgiDepartment of OMNI Biomarker Development, Genentech Inc, South San Francisco, California, USA.
Hartmut KoeppenDepartment of Research Pathology, Genentech Inc, South San Francisco, California, USA.
Priti S HegdeFoundation Medicine, Cambridge, Massachusetts, USA.
Ira MellmanDepartment of Cancer Immunology, Genentech Inc, South San Francisco, California, USA.
W Rodney MathewsDepartment of OMNI Biomarker Development, Genentech Inc, South San Francisco, California, USA.
Thomas PowlesBarts Cancer Center, Queen Mary University, London, UK.
Sanjeev Mariathasan *Department of Oncology Biomarker Development, Genentech Inc, South San Francisco, California, USA ogormanw@gene.com jane.grogan@gmail.com sanj@gene.com.
Jane Grogan *Department of Cancer Immunology, Genentech Inc, South San Francisco, California, USA ogormanw@gene.com jane.grogan@gmail.com sanj@gene.com.
William E O'Gorman *Department of OMNI Biomarker Development, Genentech Inc, South San Francisco, California, USA ogormanw@gene.com jane.grogan@gmail.com sanj@gene.com.ORCID 0000-0003-0753-3355
Ventana Research Corporation (United States) · USAdaptive Biotechnologies (United States) · USFoundation Medicine (United States)Queen Mary University of London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCD8+ tissue-resident memory T (T

methodsHere, we test this by combining high-dimensional single-cell modalities with bulk tumor transcriptomics from 1868 patients enrolled in lung and bladder cancer clinical trials of atezolizumab (anti-programmed cell death ligand 1 (PD-L1)).

results

conclusionsOur analyses indeed demonstrate that the presence of CD103+ CD8+ T

Indexed as

Antibodies, Monoclonal, HumanizedAntigens, CDB7-H1 AntigenBiomarkers, TumorCD8-Positive T-LymphocytesClinical Trials, Phase II as TopicClinical Trials, Phase III as TopicDatabases, GeneticGene Expression ProfilingHumansImmune Checkpoint InhibitorsIntegrin alpha ChainsLung NeoplasmsLymphocytes, Tumor-InfiltratingPhenotypeRandomized Controlled Trials as Topicalpha E integrinsAntibodies, Monoclonal, HumanizedAntigens, CDatezolizumabB7-H1 AntigenBiomarkers, TumorCD274 protein, humanImmune Checkpoint InhibitorsIntegrin alpha ChainsbiomarkersCD8-positive T-lymphocytesgene expression profilingimmunotherapylymphocytestumortumor-infiltrating

Identifiers

PMID33827905
PMCPMC8032254
OpenAlexW3149571937

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.