Evidence map›Paper›PMID 30610226›Full record

ReviewNature reviews. Drug discovery2019

Approaches to treat immune hot, altered and cold tumours with combination immunotherapies.

Jérôme Galon, Daniela Bruni

2 registry-linked trialsAbstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Drug discovery, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 2,067 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2,067citing papers in PubMed, 2 pooled it
161.2field-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.

NCT04850755 phase1completednot on this mapstarted 2021, after this paper: background citation

A Phase I Dose Escalation Study of Selinexor Plus Nivolumab and Ipilimumab in Advanced/Metastatic Solid Malignancies

TypeinterventionalSponsorNational University Hospital, SingaporeRan2021 to 2025Enrolled11ConditionsAdvance Solid Malignancies, Metastatic Solid MalignanciesArmsSelinexor in combination with nivolumab and ipilimumab
NCT05405270 recruitingnot on this mapstarted 2022, after this paper: background citation

Predicting Response In Cervical Intraepithelial Neoplasia to Topical Imiquimod Treatment

Typeobservational_patient_registrySponsorCatharina Ziekenhuis EindhovenRan2022 to 2026Enrolled410ConditionsCervical High Grade Squamous Intraepithelial Lesion, Cervical Intraepithelial Neoplasia Grade 2/3, CIN 2/3, Cervical Intraepithelial NeoplasiaArmsImiquimod, 3x vaginal swab for microbiome analysis, Expectative management, 2x vaginal swab for microbiome analysis
3 · Its place in the literature

Who cites it

2,067 citing papers in PubMed, 2 syntheses or guidelines pooled it, 3,331 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. Trial
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Review
  16. Review
  17. Article
  18. Article
  19. Review
  20. Article

2,007 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

2 authors at 2 institutions in 1 country.

Jérôme GalonINSERM, Laboratory of Integrative Cancer Immunology, Sorbonne Université, Sorbonne Paris Cité, Université Paris Descartes, Université Paris Diderot, Centre de Recherche des Cordeliers, Paris, France. jerome.galon@crc.jussieu.fr.ORCID http://orcid.org/0000-0001-9635-1339
Daniela BruniINSERM, Laboratory of Integrative Cancer Immunology, Sorbonne Université, Sorbonne Paris Cité, Université Paris Descartes, Université Paris Diderot, Centre de Recherche des Cordeliers, Paris, France.
Délégation Paris 5 · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immunotherapies are the most rapidly growing drug class and have a major impact in oncology and on human health. It is increasingly clear that the effectiveness of immunomodulatory strategies depends on the presence of a baseline immune response and on unleashing of pre-existing immunity. Therefore, a general consensus emerged on the central part played by effector T cells in the antitumour responses. Recent technological, analytical and mechanistic advances in immunology have enabled the identification of patients who are more likely to respond to immunotherapy. In this Review, we focus on defining hot, altered and cold tumours, the complexity of the tumour microenvironment, the Immunoscore and immune contexture of tumours, and we describe approaches to treat such tumours with combination immunotherapies, including checkpoint inhibitors. In the upcoming era of combination immunotherapy, it is becoming critical to understand the mechanisms responsible for hot, altered or cold immune tumours in order to boost a weak antitumour immunity. The impact of combination therapy on the immune response to convert an immune cold into a hot tumour will be discussed.

Indexed as

Molecular Targeted TherapyAnimalsCancer VaccinesCombined Modality TherapyHumansImmunotherapyNeoplasmsTumor MicroenvironmentCancer Vaccines

Identifiers

PMID30610226
OpenAlexW2907564726

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.