Evidence map›Paper›PMID 36497187›Full record

ReviewCells2022

FGFR Inhibitors in Cholangiocarcinoma-A Novel Yet Primary Approach: Where Do We Stand Now and Where to Head Next in Targeting This Axis?

Paulina Chmiel, Katarzyna Gęca, Karol Rawicz-Pruszyński, Wojciech P Polkowski, Magdalena Skórzewska

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.4field-weighted citation impact, top 10% 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

20 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
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  6. Review
  7. Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. New Therapeutic Targets in RAS Wild-type Pancreatic Cancer.Current treatment options in oncology · 2024
    Review
  14. Review
  15. Article
  16. Article
  17. Molecular Profile of Intrahepatic Cholangiocarcinoma.International journal of molecular sciences · 2023
    Review
  18. Review
  19. Review
  20. Mechanisms ofIntegrative cancer therapies
    Review
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

5 authors at 1 institution in 1 country.

Paulina ChmielDepartment of Surgical Oncology, Medical University of Lublin, 20-080 Lublin, Poland.
Katarzyna GęcaDepartment of Surgical Oncology, Medical University of Lublin, 20-080 Lublin, Poland.ORCID 0000-0001-5024-2559
Karol Rawicz-PruszyńskiDepartment of Surgical Oncology, Medical University of Lublin, 20-080 Lublin, Poland.ORCID 0000-0002-2555-2114
Wojciech P PolkowskiDepartment of Surgical Oncology, Medical University of Lublin, 20-080 Lublin, Poland.ORCID 0000-0001-6455-5636
Magdalena SkórzewskaDepartment of Surgical Oncology, Medical University of Lublin, 20-080 Lublin, Poland.
Medical University of Lublin · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cholangiocarcinomas (CCAs) are rare but aggressive tumours with poor diagnosis and limited treatment options. Molecular targeted therapies became a promising proposal for patients after progression under first-line chemical treatment. In light of an escalating prevalence of CCA, it is crucial to fully comprehend its pathophysiology, aetiology, and possible targets in therapy. Such knowledge would play a pivotal role in searching for new therapeutic approaches concerning diseases' symptoms and their underlying causes. Growing evidence showed that fibroblast growth factor/fibroblast growth factor receptor (FGF/FGFR) pathway dysregulation is involved in a variety of processes during embryonic development and homeostasis as well as tumorigenesis. CCA is known for its close correlation with the FGF/FGFR pathway and targeting this axis has been proposed in treatment guidelines. Bearing in mind the significance of molecular targeted therapies in different neoplasms, it seems most reasonable to move towards intensive research and testing on these in the case of CCA. However, there is still a need for more data covering this topic. Although positive results of many pre-clinical and clinical studies are discussed in this review, many difficulties lie ahead. Furthermore, this review presents up-to-date literature regarding the outcomes of the latest clinical data and discussion over future directions of FGFR-directed therapies in patients with CCA.

Indexed as

Bile Duct NeoplasmsCholangiocarcinomaBile Ducts, IntrahepaticHumansProtein Kinase InhibitorsReceptors, Fibroblast Growth FactorProtein Kinase InhibitorsReceptors, Fibroblast Growth FactorCCAcholangiocarcinomaFGFRtargeted therapytherapy resistanceTKIs

Identifiers

PMID36497187
PMCPMC9737583
OpenAlexW4311532817

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.