Evidence map›Paper›PMID 40562703›Full record

ArticleJournal for immunotherapy of cancer2025

Mapping immune activity in HPV-negative head and neck squamous cell carcinoma: a spatial multiomics analysis.

Natalie Zwing, Lena Voith von Voithenberg, Laurent Alberti, Sascha Michael Gabriel, Josep M Monné Rodriguez, Romi Feddersen, Jean-Philippe Foy, Francesca Damiola, Nicolas Gadot, Pierre Saintigny and 1 more

Abstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

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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

11 authors.

Natalie Zwing *Roche Pharma Research and Early Development, Roche Innovation Center Munich, F Hoffmann-La Roche Ltd, Penzberg, Germany.
Lena Voith von Voithenberg *Roche Pharma Research and Early Development, Early Development Oncology, Roche Innovation Center Zurich, F Hoffmann-La Roche Ltd, Schlieren, Switzerland lena.voith_von_voithenberg@roche.com.ORCID http://orcid.org/0000-0002-8646-2817
Laurent Alberti *INSERM 1052, CNRS 5286, Centre Léon Bérard, Centre de Recherche en Cancérologie de Lyon, Université Claude Bernard Lyon 1, Lyon, France.
Sascha Michael Gabriel *Roche Pharma Research and Early Development, Roche Innovation Center Munich, F Hoffmann-La Roche Ltd, Penzberg, Germany.
Josep M Monné RodriguezRoche Pharma Research and Early Development, Early Development Oncology, Roche Innovation Center Zurich, F Hoffmann-La Roche Ltd, Schlieren, Switzerland.
Romi FeddersenRoche Pharma Research and Early Development, Roche Innovation Center Munich, F Hoffmann-La Roche Ltd, Penzberg, Germany.
Jean-Philippe FoySorbonne University, INSERM UMRS 938 Centre de Recherche de Saint Antoine, Department of Oral and Maxillo-Facial Surgery, Pitié-Salpêtrière Hospital, Assistance Publique des Hôpitaux de Paris, Paris, France.
Francesca DamiolaPlateforme Anatomopathologie Recherche, Centre de Recherche en Cancérologie (CRCL), INSERM U1052, CNRS UMR 5286, Centre Léon Bérard, Université Claude Bernard Lyon 1, Lyon, France.
Nicolas GadotPlateforme Anatomopathologie Recherche, Centre de Recherche en Cancérologie (CRCL), INSERM U1052, CNRS UMR 5286, Centre Léon Bérard, Université Claude Bernard Lyon 1, Lyon, France.
Pierre Saintigny *INSERM 1052, CNRS 5286, Centre Léon Bérard, Centre de Recherche en Cancérologie de Lyon, Université Claude Bernard Lyon 1, Lyon, France.ORCID http://orcid.org/0000-0002-8090-9323
Bruno Gomes *Roche Pharma Research and Early Development, Early Development Oncology, Roche Innovation Center Basel, F Hoffmann-La Roche AG, Basel, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHead and neck squamous cell carcinoma (HNSCC) exhibits low response rates to immunotherapies, with only about 15-25% of patients responding to monotherapy and 30-45% to combination therapy. This limited effectiveness is attributed to significant intertumor and intratumor heterogeneity, which affects the immunological activity of individual tumors and their regions, thereby influencing immunotherapy outcomes. Various biomarkers at the gene and protein expression levels have been identified to predict the response to immunotherapy in HNSCC.

methodsIn this study, we evaluated intertumor heterogeneity using a 27-gene expression signature to stratify tumors by their immunologic activity status. We investigated intertumor heterogeneity at the molecular and cellular level and further analyzed intratumor spatial heterogeneity within and across these subgroups by using spatial multiomics approaches.

resultsImmunologically active tumors showed increased interferon-γ and interferon-α signaling and upregulation of major histocompatibility complex-I signaling and genes involved in antigen presentation. Chemokines such as

conclusionsThe spatial analysis at multiple omics levels allowed for a detailed investigation of molecular and cell type markers to further distinguish between immunologically active and immunosuppressive microenvironments and their spatial heterogeneity. Our study demonstrates that, besides gene expression signatures, cell colocalization signatures can infer immunological activity in HNSCC, thus predicting immunotherapy response.

Indexed as

Head and Neck NeoplasmsSquamous Cell Carcinoma of Head and NeckBiomarkers, TumorFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansImmunotherapyMaleMultiomicsTumor MicroenvironmentBiomarkers, TumorBiomarkerGene expression profiling - GEPHead and Neck CancerImmunotherapy

Identifiers

PMID40562703
PMCPMC12198833

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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.