Evidence map›Paper›PMID 35164813›Full record

ReviewJournal of experimental & clinical cancer research : CR2022

Blockade of novel immune checkpoints and new therapeutic combinations to boost antitumor immunity.

Adrià Archilla-Ortega, Carla Domuro, Juan Martin-Liberal, Purificación Muñoz

Abstract readReview
In one paragraph

Review in Journal of experimental & clinical cancer research : CR, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers.

0numbers the graph read from it
0cells of the map it votes in
50citing 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

50 citing papers in PubMed.

  1. cGAMP suppresses FTO expression to promote mCellular and molecular life sciences : CMLS · 2026
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  10. PD-1Journal of experimental & clinical cancer research : CR · 2025
    Article
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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

4 authors.

Adrià Archilla-OrtegaAging and Cancer Group, Oncobell Program, Bellvitge Biomedical Research Institute (IDIBELL), Av. Gran Vía de L'Hospitalet 199-203, 08907, Barcelona, Spain.
Carla DomuroAging and Cancer Group, Oncobell Program, Bellvitge Biomedical Research Institute (IDIBELL), Av. Gran Vía de L'Hospitalet 199-203, 08907, Barcelona, Spain.
Juan Martin-LiberalMedical Oncology Department, Catalan Institute of Oncology (ICO) Hospitalet, IDIBELL, Barcelona, Spain.
Purificación MuñozAging and Cancer Group, Oncobell Program, Bellvitge Biomedical Research Institute (IDIBELL), Av. Gran Vía de L'Hospitalet 199-203, 08907, Barcelona, Spain. p.munoz@idibell.cat.ORCID http://orcid.org/0000-0002-3751-2099

Funding

Government of Andorra ATC0XX - AND-2019/2020Instituto de Salud Carlos III PI19/01210Ministerio de Ciencia e Innovación PID2020-113495RB-I00Ministerio de Ciencia e Innovación SAF2017-84976R
6 · The paper itself

Abstract

Immunotherapy has emerged as a promising strategy for boosting antitumoral immunity. Blockade of immune checkpoints (ICs), which regulate the activity of cytotoxic T lymphocytes (CTLs) and natural killer (NK) cells has proven clinical benefits. Antibodies targeting CTLA-4, PD-1, and PD-L1 are IC-blockade drugs approved for the treatment of various solid and hematological malignancies. However, a large subset of patients does not respond to current anti-IC immunotherapy. An integrative understanding of tumor-immune infiltrate, and IC expression and function in immune cell populations is fundamental to the design of effective therapies. The simultaneous blockade of newly identified ICs, as well as of previously described ICs, could improve antitumor response. We review the potential for novel combinatory blockade strategies as antitumoral therapy, and their effects on immune cells expressing the targeted ICs. Preclinical evidence and clinical trials involving the blockade of the various ICs are reported. We finally discuss the rationale of IC co-blockade strategy with respect to its downstream signaling in order to improve effective antitumoral immunity and prevent an increased risk of immune-related adverse events (irAEs).

Indexed as

HumansImmune Checkpoint InhibitorsImmunityImmunotherapyKiller Cells, NaturalNeoplasmsImmune Checkpoint InhibitorsCytotoxic T lymphocytesImmune checkpointImmunotherapyNK cellsTumor microenvironment

Identifiers

PMID35164813
PMCPMC8842574

What OpenQuestion holds

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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.