Evidence map›Paper›PMID 28953502›Full record

ArticleInternational journal of gynecological cancer : official journal of the International Gynecological Cancer Society2018

Endometrial Cancers Harboring Mutated Fibroblast Growth Factor Receptor 2 Protein Are Successfully Treated With a New Small Tyrosine Kinase Inhibitor in an Orthotopic Mouse Model.

Sebastien Taurin, Chieh-Hsiang Yang, Maria Reyes, Sungpil Cho, Demetrius M Coombs, Elke A Jarboe, Theresa L Werner, C Matthew Peterson, Margit M Janát-Amsbury

Open access · greenAbstract read
In one paragraph

Article in International journal of gynecological cancer : official journal of the International Gynecological Cancer Society, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 7% 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

59 citing papers in PubMed, 1 synthesis or guideline pooled it, 86 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Trial
  6. Trial
  7. Trial
  8. Trial
  9. Article
  10. Review
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  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

9 authors at 5 institutions in 1 country.

Sebastien Taurin
Chieh-Hsiang Yang
Maria Reyes
Sungpil Cho
Demetrius M Coombs
Elke A Jarboe
Theresa L Werner
C Matthew Peterson
Margit M Janát-Amsbury
University of Utah · USUtah Department of Health · USDrexel University · USHuntsman Cancer Institute · USUniversity of Utah Health Care · US

Funding

Intelligent Polymeric Nanogel Technology Overcoming Drug Resistance in Ovarian CaR01CA140348 · NCI · UNIVERSITY OF UTAH · PI BAE, YOU HAN, JANAT-AMSBURY, MARGIT MARIA · 2009 to 2010
$624k
Multiplexed Ovarian Cancer Microfluidic Tissue MicroarrayR43CA177146 · NCI · CARTERRA, INC. · PI BROOKS, BENJAMIN DELBERT, JANAT-AMSBURY, MARGIT MARIA · 2014 to 2014
$225k
NCI NIH HHS R01 CA140348NCI NIH HHS R43 CA177146
6 · The paper itself

Abstract

objectivesAL3818 (anlotinib) is a receptor tyrosine kinase inhibitor targeting vascular endothelial growth factor receptors (VEGFR1, VEGFR2/KDR, and VEGFR3), stem cell factor receptor (C-kit), platelet-derived growth factor (PDGFβ), and fibroblast growth factor receptors (FGFR1, FGFR2, and FGFR3). This study evaluates the efficacy of AL3818 studying tumor regression in an orthotopic murine endometrial cancer model.

methodsWe tested the cytotoxicity of AL3818 on a panel of 7 human endometrial cancer cell lines expressing either wild-type or mutant FGFR2 and also assessed the in vivo antitumor efficacy in a murine, orthotopic AN3CA endometrial cancer model. AL3818 was administered daily per os either alone or in combination with carboplatin and paclitaxel, which represent the current standard of adjuvant care for endometrial cancer.

resultsAL3818 significantly reduces AN3CA cell number in vitro, characterized by high expression of a mutated FGFR2 protein. Daily oral administration of AL3818 (5 mg/kg) resulted in a complete response in 55% of animals treated and in a reduced tumor volume, as well as decreased tumor weights of AN3CA tumors by 94% and 96%, respectively, following a 29-day treatment cycle. Whereas carboplatin and paclitaxel failed to alter tumor growth, the combination with AL3818 did not seem to exhibit a superior effect when compared with AL3818 treatment alone.

conclusionsAL3818 shows superior efficacy for the treatment of endometrial cancer irresponsive to conventional carboplatin and paclitaxel combination and warrants further investigation.

Indexed as

MutationAnimalsAntineoplastic Combined Chemotherapy ProtocolsCarboplatinCell Growth ProcessesCell Line, TumorEndometrial NeoplasmsFemaleHumansIndolesMiceMice, NudePaclitaxelProtein Kinase InhibitorsQuinolinesRandom AllocationanlotinibCarboplatinFGFR2 protein, humanIndolesPaclitaxelProtein Kinase InhibitorsQuinolinesReceptor, Fibroblast Growth Factor, Type 2

Identifiers

PMID28953502
PMCPMC5735020
OpenAlexW2756743534

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.