Evidence map›Paper›PMID 37620318›Full record

ArticleNature communications2023

Acquired resistance to anti-PD1 therapy in patients with NSCLC associates with immunosuppressive T cell phenotype.

Stefanie Hiltbrunner, Lena Cords, Sabrina Kasser, Sandra N Freiberger, Susanne Kreutzer, Nora C Toussaint, Linda Grob, Isabelle Opitz, Michael Messerli, Martin Zoche and 5 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed, 2 pooled it
12.0field-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

55 citing papers in PubMed, 2 syntheses or guidelines pooled it, 52 citations in OpenAlex.

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  17. T-Cell Immunity and Lung Cancer.Respirology (Carlton, Vic.) · 2026
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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 1 country.

Stefanie HiltbrunnerDepartment of Medical Oncology and Hematology, University Hospital Zurich, Zurich, 8091, Switzerland.ORCID http://orcid.org/0000-0002-3415-7992
Lena CordsUniversity of Zurich, Zurich, Switzerland.
Sabrina KasserDepartment of Medical Oncology and Hematology, University Hospital Zurich, Zurich, 8091, Switzerland.
Sandra N FreibergerDepartment of Pathology and Molecular Pathology, University Hospital Zurich, 8091, Zurich, Switzerland.ORCID http://orcid.org/0000-0001-6874-9649
Susanne KreutzerFunctional Genomics Center Zurich, ETH and University of Zurich, Zurich, 8057, Switzerland.
Nora C ToussaintNEXUS Personalized Health Technologies, ETH Zurich, Zurich, 8952, Switzerland.ORCID http://orcid.org/0000-0001-7911-7647
Linda GrobNEXUS Personalized Health Technologies, ETH Zurich, Zurich, 8952, Switzerland.ORCID http://orcid.org/0000-0003-3817-7613
Isabelle OpitzDepartment of Thoracic Surgery, University Hospital Zurich, Zurich, 8091, Switzerland.ORCID http://orcid.org/0000-0001-5900-9040
Michael MesserliUniversity of Zurich, Zurich, Switzerland.
Martin ZocheDepartment of Pathology and Molecular Pathology, University Hospital Zurich, 8091, Zurich, Switzerland.ORCID http://orcid.org/0000-0002-0421-7229
Alex SoltermannDepartment of Pathology and Molecular Pathology, University Hospital Zurich, 8091, Zurich, Switzerland.
Markus RechsteinerDepartment of Pathology and Molecular Pathology, University Hospital Zurich, 8091, Zurich, Switzerland.
Maries van den BroekUniversity of Zurich, Zurich, Switzerland.ORCID http://orcid.org/0000-0002-9489-3692
Bernd BodenmillerUniversity of Zurich, Zurich, Switzerland.
Alessandra Curioni-FontecedroDepartment of Medical Oncology and Hematology, University Hospital Zurich, Zurich, 8091, Switzerland. alessandra.curioni-fontecedro@h-fr.ch.
University of Zurich · CHUniversity Hospital of Zurich · CHSIB Swiss Institute of Bioinformatics · CHUniversity of Fribourg · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune checkpoint inhibitor treatment has the potential to prolong survival in non-small cell lung cancer (NSCLC), however, some of the patients develop resistance following initial response. Here, we analyze the immune phenotype of matching tumor samples from a cohort of NSCLC patients showing good initial response to immune checkpoint inhibitors, followed by acquired resistance at later time points. By using imaging mass cytometry and whole exome and RNA sequencing, we detect two patterns of resistance¨: One group of patients is characterized by reduced numbers of tumor-infiltrating CD8

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsB7-H1 AntigenCD8-Positive T-LymphocytesHumansImmune Checkpoint InhibitorsImmunosuppressive AgentsPhenotypeB7-H1 AntigenImmune Checkpoint InhibitorsImmunosuppressive Agents

Identifiers

PMID37620318
PMCPMC10449840
OpenAlexW4386136986

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.