Evidence map›Paper›PMID 37649478›Full record

ReviewFrontiers in immunology2023

Tumor-associated macrophages mediate resistance of EGFR-TKIs in non-small cell lung cancer: mechanisms and prospects.

Daoan Cheng, Kele Ge, Xue Yao, Banglu Wang, Rui Chen, Weiqing Zhao, Cheng Fang, Mei Ji

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
5.4field-weighted citation impact, top 4% 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

23 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Macrophage ferroptosis in hematologic malignancies: emerging mechanisms and therapeutic implications.Apoptosis : an international journal on programmed cell death · 2026
    Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. Article
  11. Review
  12. Exosome-based immunotherapy in hepatocellular carcinoma.Clinical and experimental medicine · 2025
    Review
  13. Review
  14. Review
  15. Article
  16. Article
  17. Therapeutic advances of targeting receptor tyrosine kinases in cancer.Signal transduction and targeted therapy · 2024
    Review
  18. Review
  19. Article
  20. 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

8 authors at 1 institution in 1 country.

Daoan ChengDepartments of Oncology, the Third Affiliated Hospital of Soochow University, Changzhou, China.
Kele GeDepartments of Oncology, the Third Affiliated Hospital of Soochow University, Changzhou, China.
Xue YaoDepartments of Oncology, the Third Affiliated Hospital of Soochow University, Changzhou, China.
Banglu WangDepartments of Oncology, the Third Affiliated Hospital of Soochow University, Changzhou, China.
Rui ChenDepartments of Oncology, the Third Affiliated Hospital of Soochow University, Changzhou, China.
Weiqing ZhaoDepartments of Oncology, the Third Affiliated Hospital of Soochow University, Changzhou, China.
Cheng FangDepartments of Oncology, the Third Affiliated Hospital of Soochow University, Changzhou, China.
Mei JiDepartments of Oncology, the Third Affiliated Hospital of Soochow University, Changzhou, China.
Soochow University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs) are the first-line standard treatment for advanced non-small cell lung cancer (NSCLC) with EGFR mutation. However, resistance to EGFR-TKIs is inevitable. Currently, most studies on the mechanism of EGFR-TKIs resistance mainly focus on the spontaneous resistance phenotype of NSCLC cells. Studies have shown that the tumor microenvironment (TME) also mediates EGFR-TKIs resistance in NSCLC. Tumor-associated macrophages (TAMs), one of the central immune cells in the TME of NSCLC, play an essential role in mediating EGFR-TKIs resistance. This study aims to comprehensively review the current mechanisms underlying TAM-mediated resistance to EGFR-TKIs and discuss the potential efficacy of combining EGFR-TKIs with targeted TAMs therapy. Combining EGFR-TKIs with TAMs targeting may improve the prognosis of NSCLC with EGFR mutation to some extent.

Indexed as

Carcinoma, Non-Small-Cell LungLung NeoplasmsTyrosine Kinase InhibitorsDrug Resistance, NeoplasmErbB ReceptorsHumansMutationTumor-Associated MacrophagesTumor MicroenvironmentEGFR protein, humanErbB ReceptorsTyrosine Kinase InhibitorsEGFR-TKIsexosomeNSCLCresistancetumor-associated macrophages

Identifiers

PMID37649478
PMCPMC10463184
OpenAlexW4385876039

What OpenQuestion holds

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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.