Evidence mapPaperPMID 39000121Full record

ReviewInternational journal of molecular sciences2024

The Role of Aging and Senescence in Immune Checkpoint Inhibitor Response and Toxicity.

Sidharth S Jain, Giselle Burton Sojo, Harry Sun, Benjamin N Friedland, Megan E McNamara, Marcel O Schmidt, Anton Wellstein

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
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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

7 authors.

Sidharth S JainGeorgetown Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC 20007, USA.ORCID 0000-0002-6263-651X
Giselle Burton SojoGeorgetown Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC 20007, USA.
Harry SunGeorgetown Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC 20007, USA.ORCID 0009-0001-1181-1234
Benjamin N FriedlandGeorgetown Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC 20007, USA.
Megan E McNamaraGeorgetown Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC 20007, USA.
Marcel O SchmidtGeorgetown Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC 20007, USA.ORCID 0000-0002-3991-2766
Anton WellsteinGeorgetown Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC 20007, USA.ORCID 0000-0002-0570-4950

Funding

Tissue Culture and Biobanking Shared ResourceP30CA051008 · GEORGETOWN UNIVERSITY · 1990 to 2025
$20.3M
TRAINING GRANT IN TUMOR BIOLOGYT32CA009686 · GEORGETOWN UNIVERSITY · 1996 to 2025
$2.2M
Pharmacological Sciences Training Program (PSTP)T32GM142520 · GEORGETOWN UNIVERSITY · 2025 to 2025
$321k
Decoding the Tissue of Origin of Cellular Damage from Cell-free DNA in Liquid BiopsiesF30CA250307 · NCI · GEORGETOWN UNIVERSITY · 2024 to 2025
$109k
NCI NIH HHS F30 CA250307NCI NIH HHS R01 CA231291NCI NIH HHS T32 CA009686NIGMS NIH HHS T32 GM142520NIH HHS 3P30CA051008-28S1NIH HHS 5F30CA250307-02NIH HHS 5R01CA231291-05NIH HHS 5T32CA009686-27NIH HHS 5T32GM142520-02
6 · The paper itself

Abstract

Cellular senescence accumulates with age and has been shown to impact numerous physiological and pathological processes, including immune function. The role of cellular senescence in cancer is multifaceted, but the impact on immune checkpoint inhibitor response and toxicity has not been fully evaluated. In this review, we evaluate the impact of cellular senescence in various biological compartments, including the tumor, the tumor microenvironment, and the immune system, on immune checkpoint inhibitor efficacy and toxicity. We provide an overview of the impact of cellular senescence in normal and pathological contexts and examine recent studies that have connected aging and cellular senescence to immune checkpoint inhibitor treatment in both the pre-clinical and clinical contexts. Overall, senescence plays a multi-faceted, context-specific role and has been shown to modulate immune-related adverse event incidence as well as immune checkpoint inhibitor response.

Indexed as

Cellular SenescenceImmune Checkpoint InhibitorsNeoplasmsTumor MicroenvironmentAgingAnimalsHumansImmune Checkpoint Inhibitorsagingcellular senescenceimmune checkpoint inhibitorimmune-related adverse events

Identifiers

PMID39000121
PMCPMC11241020

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.