Evidence map›Paper›PMID 33686237›Full record

ReviewNature reviews. Drug discovery2021

Beyond immune checkpoint blockade: emerging immunological strategies.

Shawn P Kubli, Thorsten Berger, Daniel V Araujo, Lillian L Siu, Tak W Mak

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Drug discovery, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 251 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
251citing papers in PubMed, 1 pooled it
34.3field-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.

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

251 citing papers in PubMed, 1 synthesis or guideline pooled it, 466 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Targeting BCL9/BCL9L enhances CD4Acta pharmacologica Sinica · 2026
    Article
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  8. Phase I Trial of Ipatasertib plus Atezolizumab Enhances PI3K/AKT Pathway Immune Responses in Solid Tumors and Refractory Glioblastoma.Clinical cancer research : an official journal of the American Association for Cancer Research · 2026
    Article
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  10. Universal off-the-shelf TGF-Acta pharmaceutica Sinica. B · 2026
    Article
  11. Article
  12. Review
  13. FN1Oncogene · 2026
    Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. Article

191 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

5 authors at 2 institutions in 2 countries.

Shawn P KubliOntario Cancer Institute, Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Thorsten BergerOntario Cancer Institute, Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Daniel V AraujoDivision of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.ORCID http://orcid.org/0000-0002-7013-5408
Lillian L SiuDivision of Medical Oncology and Hematology, Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada.
Tak W MakOntario Cancer Institute, Princess Margaret Cancer Centre, University Health Network, Toronto, ON, Canada. tmak@uhnres.utoronto.ca.
University Health Network · CAUniversity of Toronto · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The success of checkpoint inhibitors has accelerated the clinical implementation of a vast mosaic of single agents and combination immunotherapies. However, the lack of clinical translation for a number of immunotherapies as monotherapies or in combination with checkpoint inhibitors has clarified that new strategies must be employed to advance the field. The next chapter of immunotherapy should examine the immuno-oncology therapeutic failures, and consider the complexity of immune cell-cancer cell interactions to better design more effective anticancer drugs. Herein, we briefly review the history of immunotherapy and checkpoint blockade, highlighting important clinical failures. We discuss the critical aspects - beyond T cell co-receptors - of immune processes within the tumour microenvironment (TME) that may serve as avenues along which new therapeutic strategies in immuno-oncology can be forged. Emerging insights into tumour biology suggest that successful future therapeutics will focus on two key factors: rescuing T cell homing and dysfunction in the TME, and reappropriating mononuclear phagocyte function for TME inflammatory remodelling. New drugs will need to consider the complex cell networks that exist within tumours and among cancer types.

Indexed as

Immune Checkpoint InhibitorsNeoplasmsAntineoplastic AgentsHumansImmunotherapyTumor MicroenvironmentAntineoplastic AgentsImmune Checkpoint Inhibitors

Identifiers

PMID33686237
OpenAlexW3134659811

What OpenQuestion holds

Textmetadata
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.