Evidence mapPaperPMID 41680842Full record

ReviewCancer cell international2026

Multi-tyrosine kinase inhibitors: exploring immunomodulatory effects on various immune cell types in cancer.

Fatemeh Keshavarz, Mohsen Soltanshahi, Malaksima Ayadilord, Faezeh Mortazavi, Mahdi Shabani, Seyed Amir Jalali

Abstract readReview
In one paragraph

Review in Cancer cell international, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

6 authors.

Fatemeh KeshavarzDepartment of Immunology, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Mohsen SoltanshahiDepartment of Immunology, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Malaksima AyadilordDepartment of Immunology, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Faezeh MortazaviIranian Blood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Tehran, Iran.
Mahdi ShabaniDepartment of Immunology, Shahid Beheshti University of Medical Sciences, Tehran, Iran. msshabani@yahoo.com.
Seyed Amir JalaliDepartment of Immunology, Shahid Beheshti University of Medical Sciences, Tehran, Iran. jalali5139@yahoo.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

TKIs, or tyrosine kinase inhibitors, are pharmaceutical agents used in cancer treatment because they can block or inhibit enzymes called tyrosine kinases. These enzymes are essential in regulating cell processes such as growth, differentiation, metabolism, and survival. Multi-TKIs target several tyrosine kinases at once, improving therapeutic outcomes while affecting multiple signaling pathways simultaneously. However, a major challenge with multi-TKIs is that they often impact normal cells that rely on the same pathways, creating a need to balance treatment effectiveness with manageable side effects. TKIs play a crucial role in immune system regulation by modifying cell activation and development, either enhancing or suppressing immune responses. They can influence various cells in both innate and adaptive immunity and act on immunological checkpoints that control T cell activity. Additionally, TKIs can be part of resistance mechanisms, requiring careful understanding of their effects. Gaining insight into how TKIs interact with the immune system enhances patient care and improves medication efficacy.

Indexed as

CancerImmune cellImmunomodulatoryImmunotherapyTKI

Identifiers

PMID41680842
PMCPMC12998203

What Socratic holds

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LicenceCC BY-NC-ND
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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 Socratic graph.