Evidence map›Paper›PMID 34676147›Full record

ReviewOncoimmunology2021

Trial watch: intratumoral immunotherapy.

Juliette Humeau, Julie Le Naour, Lorenzo Galluzzi, Guido Kroemer, Jonathan G Pol

Registry-linked trialOpen access · goldAbstract readReview
In one paragraph

Review in Oncoimmunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05751837 (Feasibility Study of Intra-Tumoral Lipopolysaccharide Immunotherapy for Intra-Abdominal Tumors), which is not on this map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
4.0field-weighted citation impact, top 4% 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.

NCT05751837 phase1completednot on this mapstarted 2023, after this paper: background citation

Feasibility Study of Intra-Tumoral Lipopolysaccharide Immunotherapy for Intra-Abdominal Tumors

TypeinterventionalSponsorPatrick Wagner, MD, FACSRan2023 to 2024Enrolled12ConditionsAbdominal Cancer, MalignancyArmsLipopolysaccharide
3 · Its place in the literature

Who cites it

38 citing papers in PubMed, 57 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
  4. Tumor-embedded Immunity and TRM Cell Functions in Cancer.Mini reviews in medicinal chemistry · 2026
    Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Article
  15. Review
  16. Immunotherapies for locally aggressive cancers.Advanced drug delivery reviews · 2024
    Review
  17. Article
  18. Review
  19. Article
  20. CD8Nature communications · 2024
    Article
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

5 authors at 4 institutions in 6 countries.

Juliette HumeauCanada Department of Medicine, Institute for Research in Immunology and Cancer (Iric), Université de Montréal, Montreal, QC, Canada.ORCID 0000-0002-1991-8001
Julie Le NaourCentre de Recherche des Cordeliers, Equipe labellisée par la Ligue contre le cancer, INSERM, Sorbonne Université, Université de Paris, Paris, France.ORCID 0000-0002-3749-2171
Lorenzo GalluzziDepartment of Radiation Oncology, Weill Cornell Medical College, New York, NY, USA.ORCID 0000-0003-2257-8500
Guido KroemerCentre de Recherche des Cordeliers, Equipe labellisée par la Ligue contre le cancer, INSERM, Sorbonne Université, Université de Paris, Paris, France.ORCID 0000-0002-9334-4405
Jonathan G PolCentre de Recherche des Cordeliers, Equipe labellisée par la Ligue contre le cancer, INSERM, Sorbonne Université, Université de Paris, Paris, France.ORCID 0000-0002-8355-7562
Université Paris-Saclay · FRCornell University · USInstitut Gustave Roussy · FRKarolinska University Hospital · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

While chemotherapy and radiotherapy remain the first-line approaches for the management of most unresectable tumors, immunotherapy has emerged in the past two decades as a game-changing treatment, notably with the clinical success of immune checkpoint inhibitors. Immunotherapies aim at (re)activating anticancer immune responses which occur in two main steps: (1) the activation and expansion of tumor-specific T cells following cross-presentation of tumor antigens by specialized myeloid cells (priming phase); and (2) the immunological clearance of malignant cells by these antitumor T lymphocytes (effector phase). Therapeutic vaccines, adjuvants, monoclonal antibodies, cytokines, immunogenic cell death-inducing agents including oncolytic viruses, anthracycline-based chemotherapy and radiotherapy, as well as adoptive cell transfer, all act at different levels of this cascade to (re)instate cancer immunosurveillance. Intratumoral delivery of these immunotherapeutics is being tested in clinical trials to promote superior antitumor immune activity in the context of limited systemic toxicity.

Indexed as

NeoplasmsOncolytic VirusesAntibodies, MonoclonalHumansImmunologic FactorsImmunotherapyAntibodies, MonoclonalImmunologic FactorsAntitumor immunitycancer immunosurveillanceimmunotherapyin situ vaccinationintralesional injection

Identifiers

PMID34676147
PMCPMC8526014
OpenAlexW3205381631

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.