Evidence map›Paper›PMID 30523282›Full record

ReviewNature reviews. Clinical oncology2019

Cancer immunoediting and resistance to T cell-based immunotherapy.

Jake S O'Donnell, Michele W L Teng, Mark J Smyth

4 registry-linked trialsAbstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Clinical oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 4 registered trials, which are not on this map. Cited by 1,050 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
1,050citing papers in PubMed, 2 pooled it
46.1field-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.

NCT05173246 phase2recruitingnot on this mapstarted 2020, after this paper: background citation

JS001 Combined With Nab-paclitaxel and Cisplatin or Carboplatin as First-line Treatment for Unresectable or Advanced Small Cell Esophageal Carcinoma : a Prospective, Single Arm, Multicenter, Phase II Clinical Trial

TypeinterventionalSponsorSun Yat-sen UniversityRan2020 to 2026Enrolled43ConditionsEsophageal Small Cell CarcinomaArmsJS001, nab-paclitaxel, Cisplatin, Carboplatin
NCT05546619 naunknown statusnot on this mapstarted 2022, after this paper: background citation

Research on Effectiveness and Safety of the Treatment, Hyperthermic Intraperitoneal Chemotherapy Combined With Tislelizumab and Targeted Therapy, That is Used for High-risk Hepatocellular Carcinoma After R0 Resection

TypeinterventionalSponsorSulai LiuRan2022 to 2025Enrolled30ConditionsHepatocellular CarcinomaArmsHIPEC+tislelizumab + targeted therapy
NCT05929092 naunknown statusnot on this mapstarted 2023, after this paper: background citation

Total Body Irradiation/ Fludarabine/ Busulfan/ Cyclophosphamide (TFBC) Combined With Umbilical Cord Blood Transplantation (UCBT) in the Treatment of High-risk Malignant Hematological Diseases

TypeinterventionalSponsorThe First Affiliated Hospital of Soochow UniversityRan2023 to 2026Enrolled40ConditionsHematopoietic Stem Cell Transplantation, Malignant Hematological DiseasesArmsUmbilical Cord Blood Transplantation
NCT05986981 phase2unknown statusnot on this mapstarted 2023, after this paper: background citation

Single-arm, Open-label Clinical Study on the Safety, Tolerability, and Preliminary Efficacy of MUC1 Therapeutic Tumor Vaccine in Advanced Solid Cancers

TypeinterventionalSponsorPeking Union Medical College HospitalRan2023 to 2024Enrolled20ConditionsSolid Tumor, AdultArmsVaccine
3 · Its place in the literature

Who cites it

1,050 citing papers in PubMed, 2 syntheses or guidelines pooled it, 1,751 citations in OpenAlex.

  1. Pooled it
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  11. Quantitative nanoscale imaging shows peptide-MHC I complexes are monomeric and spatially regulated in human dendritic cells.Proceedings of the National Academy of Sciences of the United States of America · 2026
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  14. European journal of nuclear medicine and molecular imaging · 2026
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  17. Universal off-the-shelf TGF-Acta pharmaceutica Sinica. B · 2026
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990 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

3 authors at 1 institution in 1 country.

Jake S O'DonnellImmunology in Cancer and Infection Laboratory, QIMR Berghofer Medical Research Institute, Queensland, Australia.
Michele W L Teng *Cancer Immunoregulation and Immunotherapy Laboratory, QIMR Berghofer Medical Research Institute, Queensland, Australia. Michele.Teng@qimrberghofer.edu.au.
Mark J Smyth *Immunology in Cancer and Infection Laboratory, QIMR Berghofer Medical Research Institute, Queensland, Australia. Mark.Smyth@qimrberghofer.edu.au.ORCID http://orcid.org/0000-0001-7098-7240
The University of Queensland · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Anticancer immunotherapies involving the use of immune-checkpoint inhibitors or adoptive cellular transfer have emerged as new therapeutic pillars within oncology. These treatments function by overcoming or relieving tumour-induced immunosuppression, thereby enabling immune-mediated tumour clearance. While often more effective and better tolerated than traditional and targeted therapies, many patients have innate or acquired resistance to immunotherapies. Cancer immunoediting is the process whereby the immune system can both constrain and promote tumour development, which proceeds through three phases termed elimination, equilibrium and escape. Throughout these phases, tumour immunogenicity is edited, and immunosuppressive mechanisms that enable disease progression are acquired. The mechanisms of resistance to immunotherapy seem to broadly overlap with those used by cancers as they undergo immunoediting to evade detection by the immune system. In this Review, we discuss how a deeper understanding of the mechanisms underlying the cancer immunoediting process can provide insight into the development of resistance to immunotherapies and the strategies that can be used to overcome such resistance.

Indexed as

Drug Resistance, NeoplasmAdoptive TransferDisease ProgressionHumansImmunologic FactorsImmunotherapyNeoplasmsT-LymphocytesTumor MicroenvironmentImmunologic Factors

Identifiers

PMID30523282
OpenAlexW2902185751

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.