Evidence map›Paper›PMID 40277912›Full record

ReviewCells2025

Resistance in Lung Cancer Immunotherapy and How to Overcome It: Insights from the Genetics Perspective and Combination Therapies Approach.

Paweł Zieliński, Maria Stępień, Hanna Chowaniec, Kateryna Kalyta, Joanna Czerniak, Martyna Borowczyk, Ewa Dwojak, Magdalena Mroczek, Grzegorz Dworacki, Antonina Ślubowska and 3 more

Abstract readReview
In one paragraph

Review in Cells, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Review
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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

13 authors.

Paweł ZielińskiChair of Pathomorphology and Clinical Immunology, Poznan University of Medical Sciences, 61-701 Poznan, Poland.ORCID 0000-0002-8552-2566
Maria StępieńUniversité Paris-Saclay, UVSQ, INSERM, END-ICAP, 94805 Versailles, France.ORCID 0000-0002-3377-4665
Hanna ChowaniecChair of Pathomorphology and Clinical Immunology, Poznan University of Medical Sciences, 61-701 Poznan, Poland.ORCID 0009-0004-7928-1702
Kateryna KalytaFaculty of Biology, University of Basel, 4123 Basel, Switzerland.ORCID 0009-0008-9535-7382
Joanna CzerniakChair of Pathomorphology and Clinical Immunology, Poznan University of Medical Sciences, 61-701 Poznan, Poland.ORCID 0009-0009-4033-6645
Martyna BorowczykDepartment of Endocrinology, Internal Medicine and Metabolism, Poznan University of Medical Sciences, 61-701 Poznan, Poland.ORCID 0000-0002-4824-8131
Ewa DwojakChair of Pathomorphology and Clinical Immunology, Poznan University of Medical Sciences, 61-701 Poznan, Poland.
Magdalena MroczekDepartment of Neurology, University Hospital Basel, 4123 Basel, Switzerland.ORCID 0000-0002-8731-0540
Grzegorz DworackiChair of Pathomorphology and Clinical Immunology, Poznan University of Medical Sciences, 61-701 Poznan, Poland.
Antonina ŚlubowskaDepartment of Biostatistics and Research Methodology, Faculty of Medicine, Collegium Medicum, Cardinal Stefan Wyszynski University of Warsaw, 02-004 Warsaw, Poland.
Hanna MarkiewiczDepartment of Histology and Embryology, Faculty of Medicine, Medical University of Warsaw, 02-004 Warsaw, Poland.ORCID 0009-0001-2548-0552
Rafał AłtynIT Department, Poznan University of Medical Sciences, 61-701 Poznan, Poland.
Paula DoboszChair of Pathomorphology and Clinical Immunology, Poznan University of Medical Sciences, 61-701 Poznan, Poland.ORCID 0000-0002-5134-0975

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lung cancer with the highest number of new cases diagnosed in Europe and in Poland, remains an example of malignancy with a very poor prognosis despite the recent progress in medicine. Different treatment strategies are now available for cancer therapy based on its type, molecular subtype and other factors including overall health, the stage of disease and cancer molecular profile. Immunotherapy is emerging as a potential addition to surgery, chemotherapy, radiotherapy or other targeted therapies, but also considered a mainstay therapy mode. This combination is an area of active investigation in order to enhance efficacy and overcome resistance. Due to the complexity and dynamic of cancer's ecosystem, novel therapeutic targets and strategies need continued research into the cellular and molecular mechanisms within the tumour microenvironment. From the genetic point of view, several signatures ranging from a few mutated genes to hundreds of them have been identified and associated with therapy resistance and metastatic potential. ML techniques and AI can enhance the predictive potential of genetic signatures and model the prognosis. Here, we present the overview of already existing treatment approaches, the current findings of key aspects of immunotherapy, such as immune checkpoint inhibitors (ICIs), existing molecular biomarkers like PD-L1 expression, tumour mutation burden, immunoscore, and neoantigens, as well as their roles as predictive markers for treatment response and resistance.

Indexed as

Drug Resistance, NeoplasmImmunotherapyLung NeoplasmsBiomarkers, TumorCombined Modality TherapyHumansImmune Checkpoint InhibitorsTumor MicroenvironmentBiomarkers, TumorImmune Checkpoint Inhibitorscheckpoint inhibitorsimmunotherapy resistancelung cancertumour microenvironment

Identifiers

PMID40277912
PMCPMC12026305

What Socratic 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 Socratic graph.