Evidence map›Paper›PMID 28356330›Full record

ReviewMolecular cancer research : MCR2017

Cancer Immunotherapy: Whence and Whither.

Peter J Stambrook, John Maher, Farzin Farzaneh

Abstract readReview
In one paragraph

Review in Molecular cancer research : MCR, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Article
  5. Review
  6. Cellular immunotherapies for cancer.Irish journal of medical science · 2021
    Review
  7. Review
  8. Tipping the Scales With Zebrafish to Understand Adaptive Tumor Immunity.Frontiers in cell and developmental biology · 2021
    Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Kras and Tumor Immunity: Friend or Foe?Cold Spring Harbor perspectives in medicine · 2018
    Review
  18. The role of neoantigen in immune checkpoint blockade therapy.Experimental hematology & oncology · 2018
    Review
  19. Review
  20. Review
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

3 authors.

Peter J StambrookDepartment of Molecular Genetics, Biochemistry and Microbiology, University of Cincinnati College of Medicine, Cincinnati, Ohio. peter.stambrook@uc.edu.
John MaherKings College London, CAR Mechanics Group, Guy's Hospital, London, United Kingdom.
Farzin FarzanehDivision of Cancer Studies, Department of Haematological Medicine, Kings College London, London, United Kingdom.

Funding

Environmental exposure: Susceptibility alleles in a DNA damage response pathwayR01ES016625 · NIEHS · UNIVERSITY OF CINCINNATI · PI STAMBROOK, PETER J. · 2009 to 2013
$2.5M
NIEHS NIH HHS R01 ES016625
6 · The paper itself

Abstract

The current concepts and practice of cancer immunotherapy evolved from classical experiments that distinguished "self" from "non-self" and the finding that humoral immunity is complemented by cellular immunity. Elucidation of the biology underlying immune checkpoints and interactions between ligands and ligand receptors that govern the immune system's ability to recognize tumor cells as foreign has led to the emergence of new strategies that mobilize the immune system to reverse this apparent tolerance. Some of these approaches have led to new therapies such as the use of mAbs to interfere with the immune checkpoint. Others have exploited molecular technologies to reengineer a subset of T cells to directly engage and kill tumor cells, particularly those of B-cell malignancies. However, before immunotherapy can become a more effective method of cancer care, there are many challenges that remain to be addressed and hurdles to overcome. Included are manipulation of tumor microenvironment (TME) to enhance T effector cell infiltration and access to the tumor, augmentation of tumor MHC expression for adequate presentation of tumor associated antigens, regulation of cytokines and their potential adverse effects, and reduced risk of secondary malignancies as a consequence of mutations generated by the various forms of genetic engineering of immune cells. Despite these challenges, the future of immunotherapy as a standard anticancer therapy is encouraging.

Indexed as

AdenosineCytokinesHumansImmune ToleranceImmunotherapyMajor Histocompatibility ComplexMutationNeoplasmsReceptors, Antigen, T-CellT-LymphocytesTumor MicroenvironmentAdenosineCytokinesReceptors, Antigen, T-Cell

Identifiers

PMID28356330
PMCPMC5457704

What OpenQuestion holds

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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.