Evidence map›Paper›PMID 35054474›Full record

ReviewLife (Basel, Switzerland)2022

FGFR Pathway Inhibition in Gastric Cancer: The Golden Era of an Old Target?

Csongor G Lengyel, Sadaqat Hussain, Andreas Seeber, Sara Jamil Nidhamalddin, Dario Trapani, Baker S Habeeb, Essam Elfaham, Syed Ayub Mazher, Fahmi Seid, Shah Z Khan and 4 more

Open access · goldAbstract readReview
In one paragraph

Review in Life (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

18 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Review
  5. Article
  6. Review
  7. Review
  8. Article
  9. Review
  10. Perioperative Tailored Treatments for Gastric Cancer: Times Are Changing.International journal of molecular sciences · 2023
    Review
  11. Article
  12. Review
  13. Review
  14. Review
  15. Signaling pathways and therapeutic interventions in gastric cancer.Signal transduction and targeted therapy · 2022
    Review
  16. Review
  17. Review
  18. A novel small molecule RK-019 inhibitsFrontiers in pharmacology · 2022
    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

14 authors at 9 institutions in 9 countries.

Csongor G LengyelHead and Neck Surgery, National Institute of Oncology, 1122 Budapest, Hungary.ORCID 0000-0001-7767-516X
Sadaqat HussainOncology Department, University Hospital of Leicester, Leicester LE1 5WW, UK.
Andreas SeeberComprehensive Cancer Center Innsbruck, Department of Hematology and Oncology, Medical University of Innsbruck, 6020 Innsbruck, Austria.ORCID 0000-0001-8529-7824
Sara Jamil NidhamalddinDepartment of Medical Oncology, Hiwa Cancer Hospital, Sulayamaniyah 46001, Iraq.
Dario TrapaniEuropean Institute of Oncology, 20141 Milan, Italy.
Baker S HabeebMedical Oncology, Shaqlawa Teaching Hospital, Erbil 44001, Iraq.ORCID 0000-0001-8070-8532
Essam ElfahamDepartment of Hematoncology, Kuwait Cancer Control Center (KCCC), Kuwait City 20001, Kuwait.
Syed Ayub MazherDivision of Internal Medicine, UT Southwestern Clements University Hospital, Dallas, TX 75390, USA.
Fahmi SeidDepartment of Oncology, College of Medicine and Health Sciences, Hawassa University, Hawassa 1560, Ethiopia.ORCID 0000-0002-4983-890X
Shah Z KhanDepartment of Clinical Oncology, BINOR Cancer Hospital, Bannu 28000, Pakistan.ORCID 0000-0002-3692-6150
Khalid El BairiCancer Biomarkers Working Group, Oujda 60000, Morocco.ORCID 0000-0002-8414-4145
Andrew OdhiamboUnit of Medical Oncology, Department of Clinical Medicine, University of Nairobi, Nairobi 00202, Kenya.ORCID 0000-0002-7275-2186
Sara C AltunaOncomédica C. A., Caracas 1040, Venezuela.
Angelica PetrilloMedical Oncology Unit, Ospedale del Mare, 80147 Naples, Italy.ORCID 0000-0001-5489-5733
Baghdad Medical City · IQEuropean Institute of Oncology · ITHawassa University · ETInnsbruck Medical University · ATKuwait Cancer Control Center · KWLeicester General Hospital · GBNational Institute of Oncology · HUUniversity of Nairobi · KEWilliam P. Clements Jr. University Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gastric cancer (GC) is the third leading cause of cancer-associated death worldwide. The majority of patients are diagnosed at an advanced/metastatic stage of disease due to a lack of specific symptoms and lack of screening programs, especially in Western countries. Thus, despite the improvement in GC therapeutic opportunities, the survival is disappointing, and the definition of the optimal treatment is still an unmet need. Novel diagnostic techniques were developed in clinical trials in order to characterize the genetic profile of GCs and new potential molecular pathways, such as the Fibroblast Growth Factor Receptor (FGFR) pathway, were identified in order to improve patient's survival by using target therapies. The aim of this review is to summarize the role and the impact of FGFR signaling in GC and to provide an overview regarding the potential effectiveness of anti-FGFR agents in GC treatment in the context of precision medicine.

Indexed as

bemarituzumabFGFR fusionsFGFR inhibitorsfibroblast growth factor receptorsfirst linenext generation sequencingprecision medicinetarget therapyTyrosine kinase inhibitors

Identifiers

PMID35054474
PMCPMC8778800
OpenAlexW4205287605

What OpenQuestion 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 OpenQuestion graph.