Evidence map›Paper›PMID 30940805›Full record

ArticleNature communications2019

Crizotinib-induced immunogenic cell death in non-small cell lung cancer.

Peng Liu, Liwei Zhao, Jonathan Pol, Sarah Levesque, Adriana Petrazzuolo, Christina Pfirschke, Camilla Engblom, Steffen Rickelt, Takahiro Yamazaki, Kristina Iribarren and 24 more

Erratum issuedAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 187 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
187citing papers in PubMed, 1 pooled it
–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

187 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. Review
  4. Article
  5. Article
  6. Article
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  8. Article
  9. Article
  10. Article
  11. Programmed cell death in lung cancer: mechanisms, immune responses, and therapeutics.Apoptosis : an international journal on programmed cell death · 2026
    Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Neutralization of acyl-CoA-binding protein attenuates glucocorticoid-mediated suppression of cancer immunosurveillance.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  18. Article
  19. Article
  20. Review

127 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

34 authors.

Peng LiuFaculty of Medicine, University of Paris Sud, Kremlin-Bicêtre, 94270, France.ORCID http://orcid.org/0000-0002-1682-9222
Liwei ZhaoFaculty of Medicine, University of Paris Sud, Kremlin-Bicêtre, 94270, France.
Jonathan PolCell Biology and Metabolomics Platforms, Gustave Roussy Cancer Campus, Villejuif, 94805, France.
Sarah LevesqueFaculty of Medicine, University of Paris Sud, Kremlin-Bicêtre, 94270, France.
Adriana PetrazzuoloFaculty of Medicine, University of Paris Sud, Kremlin-Bicêtre, 94270, France.
Christina PfirschkeCenter for Systems Biology, Massachusetts General Hospital Research Institute and Harvard Medical School, Boston, 02139, MA, USA.
Camilla EngblomCenter for Systems Biology, Massachusetts General Hospital Research Institute and Harvard Medical School, Boston, 02139, MA, USA.
Steffen RickeltKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, Cambridge, 02139, MA, USA.ORCID http://orcid.org/0000-0002-5224-7764
Takahiro YamazakiDepartment of Radiation Oncology, Weill Cornell Medical College, New York, 14853, NY, USA.
Kristina IribarrenCell Biology and Metabolomics Platforms, Gustave Roussy Cancer Campus, Villejuif, 94805, France.
Laura SenovillaCell Biology and Metabolomics Platforms, Gustave Roussy Cancer Campus, Villejuif, 94805, France.
Lucillia BezuFaculty of Medicine, University of Paris Sud, Kremlin-Bicêtre, 94270, France.
Erika VacchelliCell Biology and Metabolomics Platforms, Gustave Roussy Cancer Campus, Villejuif, 94805, France.
Valentina SicaCell Biology and Metabolomics Platforms, Gustave Roussy Cancer Campus, Villejuif, 94805, France.
Andréa MelisCentre de Recherche INSERM LNC-, UMR1231, Dijon, France.
Tiffany MartinCentre de Recherche INSERM LNC-, UMR1231, Dijon, France.
Lin XiaCenter for Systems Medicine, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100730, China.
Heng YangCenter for Systems Medicine, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100730, China.
Qingqing LiCenter for Systems Medicine, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100730, China.
Jinfeng ChenCenter for Systems Medicine, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100730, China.
Sylvère DurandCell Biology and Metabolomics Platforms, Gustave Roussy Cancer Campus, Villejuif, 94805, France.
Fanny AprahamianCell Biology and Metabolomics Platforms, Gustave Roussy Cancer Campus, Villejuif, 94805, France.
Deborah LefevreCell Biology and Metabolomics Platforms, Gustave Roussy Cancer Campus, Villejuif, 94805, France.
Sophie BroutinDepartment of Pharmacology, Institut Gustave Roussy, Villejuif, 94805, France.
Angelo PaciDepartment of Pharmacology, Institut Gustave Roussy, Villejuif, 94805, France.
Amaury BongersDepartment of Pharmacology, Institut Gustave Roussy, Villejuif, 94805, France.
Veronique Minard-ColinInstitut de Cancérologie, Gustave Roussy Cancer Campus (GRCC), Villejuif, 94805, France.
Eric TartourINSERM U970, Université Paris Descartes Sorbonne Paris-Cité, Paris, 75006, France.ORCID http://orcid.org/0000-0002-7323-468X
Laurence ZitvogelFaculty of Medicine, University of Paris Sud, Kremlin-Bicêtre, 94270, France.
Lionel ApetohCentre de Recherche INSERM LNC-, UMR1231, Dijon, France.
Yuting MaCenter for Systems Medicine, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100730, China.ORCID http://orcid.org/0000-0001-6267-1852
Mikael J PittetCenter for Systems Biology, Massachusetts General Hospital Research Institute and Harvard Medical School, Boston, 02139, MA, USA.
Oliver KeppFaculty of Medicine, University of Paris Sud, Kremlin-Bicêtre, 94270, France. captain.olsen@gmail.com.
Guido KroemerCell Biology and Metabolomics Platforms, Gustave Roussy Cancer Campus, Villejuif, 94805, France. kroemer@orange.fr.

Funding

The Extracellular Matrix in Tumor Progression and MetastasisU54CA163109 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI HYNES, RICHARD O · 2011 to 2015
$3.7M
NCI NIH HHS U54 CA163109
6 · The paper itself

Abstract

Immunogenic cell death (ICD) converts dying cancer cells into a therapeutic vaccine and stimulates antitumor immune responses. Here we unravel the results of an unbiased screen identifying high-dose (10 µM) crizotinib as an ICD-inducing tyrosine kinase inhibitor that has exceptional antineoplastic activity when combined with non-ICD inducing chemotherapeutics like cisplatin. The combination of cisplatin and high-dose crizotinib induces ICD in non-small cell lung carcinoma (NSCLC) cells and effectively controls the growth of distinct (transplantable, carcinogen- or oncogene induced) orthotopic NSCLC models. These anticancer effects are linked to increased T lymphocyte infiltration and are abolished by T cell depletion or interferon-γ neutralization. Crizotinib plus cisplatin leads to an increase in the expression of PD-1 and PD-L1 in tumors, coupled to a strong sensitization of NSCLC to immunotherapy with PD-1 antibodies. Hence, a sequential combination treatment consisting in conventional chemotherapy together with crizotinib, followed by immune checkpoint blockade may be active against NSCLC.

Indexed as

AnimalsAntineoplastic AgentsB7-H1 AntigenCarcinoma, Non-Small-Cell LungCell DeathCell Line, TumorCrizotinibFemaleHumansInterferon-gammaLung NeoplasmsMiceMice, Inbred C57BLProgrammed Cell Death 1 ReceptorT-LymphocytesAntineoplastic AgentsB7-H1 AntigenCrizotinibInterferon-gammaProgrammed Cell Death 1 Receptor

Identifiers

PMID30940805
PMCPMC6445096

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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.