Evidence map›Paper›PMID 32790011›Full record

ReviewThe oncologist2020

Fibroblast Growth Factor Receptor (FGFR) Inhibitors in Urothelial Cancer.

Rohan Garje, Josiah An, Mohammad Obeidat, Kranthi Kumar, Hesham A Yasin, Yousef Zakharia

Open access · greenAbstract readReview
In one paragraph

Review in The oncologist, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.5field-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

30 citing papers in PubMed, 49 citations in OpenAlex.

  1. Trial
  2. Review
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  8. Review
  9. Article
  10. Article
  11. Emerging molecular therapies in the treatment of bladder cancer.Exploration of targeted anti-tumor therapy · 2024
    Review
  12. Article
  13. Article
  14. Research and development ofRSC medicinal chemistry · 2023
    Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. The Role of Novel Bladder Cancer Diagnostic and Surveillance Biomarkers-What Should a Urologist Really Know?International journal of environmental research and public health · 2022
    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

6 authors at 2 institutions in 2 countries.

Rohan GarjeDivision of Hematology, Oncology, Blood & Marrow Transplantation, University of Iowa, Iowa City, Iowa, USA.ORCID 0000-0002-7244-5602
Josiah AnDivision of Hematology, Oncology, Blood & Marrow Transplantation, University of Iowa, Iowa City, Iowa, USA.
Mohammad ObeidatDepartment of Pathology, University of Iowa, Iowa City, Iowa, USA.
Kranthi KumarDepartment of Pathology and Lab Medicine, AIIMS, Rishikesh, India.
Hesham A YasinDivision of Hematology, Oncology, Blood & Marrow Transplantation, University of Iowa, Iowa City, Iowa, USA.
Yousef ZakhariaDivision of Hematology, Oncology, Blood & Marrow Transplantation, University of Iowa, Iowa City, Iowa, USA.
University of Iowa · USAll India Institute of Medical Sciences Raipur · IN

Funding

Viral VectorP30CA086862 · NCI · UNIVERSITY OF IOWA · PI Douglas Robert Spitz · 2000 to 2026
$70.0M
NCI NIH HHS P30 CA086862
6 · The paper itself

Abstract

Dysregulated fibroblast growth factor receptor (FGFR) signaling is associated with several cancers, including urothelial carcinoma. Preclinical studies with FGFR inhibitors have shown significant antitumor activity, which has led to clinical evaluation of multiple FGFR inhibitors. Recently, erdafitinib was approved by the U.S. Food and Drug Administration for advanced urothelial carcinoma with FGFR gene alterations as the first molecularly targeted therapy. Additional ongoing clinical trials with other types of FGFR inhibitors have shown encouraging results. This review summarizes the oncogenic signaling of FGFR alterations, completed and ongoing clinical trials of FGFR inhibitors, and resistance patterns. IMPLICATIONS FOR PRACTICE: Dysregulated fibroblast growth factor receptor (FGFR) signaling is associated with several cancers, including urothelial carcinoma. Preclinical studies with FGFR inhibitors have shown significant antitumor activity, which has led to clinical evaluation of multiple FGFR inhibitors. Most recently, erdafitinib was approved by the U.S. Food and Drug Administration for advanced urothelial carcinoma with FGFR gene alterations as the first molecularly targeted therapy. Additional ongoing clinical trials with other types of FGFR inhibitors have shown encouraging results. This review summarizes the oncogenic signaling of FGFR alterations, completed and ongoing clinical trials of FGFR inhibitors, and resistance patterns.

Indexed as

Carcinoma, Transitional CellProtein Kinase InhibitorsReceptors, Fibroblast Growth FactorUrologic NeoplasmsHumansMolecular Targeted TherapyOncogenesProtein Kinase InhibitorsReceptors, Fibroblast Growth FactorErdafitinibFGFR alterationsFGFR inhibitorsTargeted therapyUrothelial cancer

Identifiers

PMID32790011
PMCPMC7648343
OpenAlexW3048907562

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.