Evidence map›Paper›PMID 36966334›Full record

ReviewMolecular cancer2023

Unleashing the potential of combining FGFR inhibitor and immune checkpoint blockade for FGF/FGFR signaling in tumor microenvironment.

Ruiwen Ruan, Li Li, Xuan Li, Chunye Huang, Zhanmin Zhang, Hongguang Zhong, Shaocheng Zeng, Qianqian Shi, Yang Xia, Qinru Zeng and 7 more

Open access · goldFull text readReview
In one paragraph

Review in Molecular cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 85 papers.

0numbers the graph read from it
0cells of the map it votes in
85citing papers in PubMed
15.7field-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

85 citing papers in PubMed, 102 citations in OpenAlex.

  1. Trial
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  8. FGFR Inhibitor AZD4547 Disrupts Inflammatory CAF Crosstalk With Cancer Cells and Macrophages and Attenuates Metastasis in Pancreatic Cancer.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2026
    Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. FGF family in health and disease.Molecular biomedicine · 2026
    Review
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. Review

25 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

17 authors at 3 institutions in 1 country.

Ruiwen Ruan *Department of Oncology, First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi Province, 330006, China.
Li Li *Department of Oncology, First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi Province, 330006, China.
Xuan Li *Department of Oncology, First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi Province, 330006, China.
Chunye HuangDepartment of Oncology, First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi Province, 330006, China.
Zhanmin ZhangDepartment of Oncology, First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi Province, 330006, China.
Hongguang ZhongDepartment of Oncology, First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi Province, 330006, China.
Shaocheng ZengDepartment of Oncology, First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi Province, 330006, China.
Qianqian ShiDepartment of Oncology, First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi Province, 330006, China.
Yang XiaDepartment of Oncology, First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi Province, 330006, China.
Qinru ZengDepartment of Oncology, First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi Province, 330006, China.
Qin WenDepartment of Oncology, First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi Province, 330006, China.
Jingyi ChenDepartment of Oncology, First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi Province, 330006, China.
Xiaofeng DaiDepartment of Oncology, First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi Province, 330006, China.
Jianping XiongDepartment of Oncology, First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi Province, 330006, China.
Xiaojun XiangDepartment of Oncology, First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi Province, 330006, China. xjxiang_nc@163.com.
Wan LeiDepartment of Oncology, First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi Province, 330006, China. 522569951@qq.com.
Jun DengDepartment of Oncology, First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi Province, 330006, China. dengjun19871106@ncu.edu.cn.
Jiangxi Provincial Cancer Hospital · CNNanchang University · CNFirst Affiliated Hospital of Nanchang University · CN

Funding

Foundation of Jiangxi Educational Commission GJJ190116Government of Jiangxi Province 20194009Government of Jiangxi Province 20202BCD42011Jiangxi Provincial Department of Science and Technology 20202BABL216050National Natural Science Foundation of China 82260491Natural Science Foundation of Jiangxi Province 20192ACB20028Youth Science Foundation of Jiangxi Province 20204BCJ23016
6 · The paper itself

Abstract

backgroundFibroblast growth factors (FGFs) and their receptors (FGFRs) play a crucial role in cell fate and angiogenesis, with dysregulation of the signaling axis driving tumorigenesis. Therefore, many studies have targeted FGF/FGFR signaling for cancer therapy and several FGFR inhibitors have promising results in different tumors but treatment efficiency may still be improved. The clinical use of immune checkpoint blockade (ICB) has resulted in sustained remission for patients. MAIN: Although there is limited data linking FGFR inhibitors and immunotherapy, preclinical research suggest that FGF/FGFR signaling is involved in regulating the tumor microenvironment (TME) including immune cells, vasculogenesis, and epithelial-mesenchymal transition (EMT). This raises the possibility that ICB in combination with FGFR-tyrosine kinase inhibitors (FGFR-TKIs) may be feasible for treatment option for patients with dysregulated FGF/FGFR signaling.

conclusionHere, we review the role of FGF/FGFR signaling in TME regulation and the potential mechanisms of FGFR-TKI in combination with ICB. In addition, we review clinical data surrounding ICB alone or in combination with FGFR-TKI for the treatment of FGFR-dysregulated tumors, highlighting that FGFR inhibitors may sensitize the response to ICB by impacting various stages of the "cancer-immune cycle".

Indexed as

Immune Checkpoint InhibitorsNeoplasmsFibroblast Growth FactorsHumansReceptors, Fibroblast Growth FactorTumor MicroenvironmentFibroblast Growth FactorsImmune Checkpoint InhibitorsReceptors, Fibroblast Growth FactorFibroblast growth factor receptorImmune checkpoint blockadeImmunotherapyTumor microenvironment

Identifiers

PMID36966334
PMCPMC10039534
OpenAlexW4360951491

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read24
table measurements read3
identifiers read34
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.