Evidence map›Paper›PMID 30575985›Full record

ArticleHepatology (Baltimore, Md.)2019

Infigratinib Mediates Vascular Normalization, Impairs Metastasis, and Improves Chemotherapy in Hepatocellular Carcinoma.

Hung Huynh, Liek Yeow Lee, Kah Yong Goh, Richard Ong, Huai-Xiang Hao, Alan Huang, Youzhen Wang, Diana Graus Porta, Pierce Chow, Alexander Chung

Abstract read
In one paragraph

Article in Hepatology (Baltimore, Md.), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

37 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  19. Cellular based immunotherapy for primary liver cancer.Journal of experimental & clinical cancer research : CR · 2021
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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

10 authors.

Hung HuynhLaboratory of Molecular Endocrinology, Division of Molecular and Cellular Research, National Cancer Centre, Singapore.
Liek Yeow LeeLaboratory of Molecular Endocrinology, Division of Molecular and Cellular Research, National Cancer Centre, Singapore.
Kah Yong GohLaboratory of Molecular Endocrinology, Division of Molecular and Cellular Research, National Cancer Centre, Singapore.
Richard OngLaboratory of Molecular Endocrinology, Division of Molecular and Cellular Research, National Cancer Centre, Singapore.
Huai-Xiang HaoNovartis Institutes for Biomedical Research, Cambridge, MA.
Alan HuangNovartis Institutes for Biomedical Research, Cambridge, MA.
Youzhen WangOncology Drug Discovery Pharmacology, Novartis Institutes for Biomedical Research, Cambridge, MA.
Diana Graus PortaOncology Translational Research, Novartis Institutes for Biomedical Research at Basel, Basel, Switzerland.
Pierce ChowDepartment of General Surgery, Singapore General Hospital, Singapore.
Alexander ChungDepartment of General Surgery, Singapore General Hospital, Singapore.

Funding

Singapore National Medical Research Council (NMRC) NMRC/MOHIAFCat1/0009/2014Singapore National Medical Research Council (NMRC) NMRC/MOHIAFCat1/0026/2015Singapore National Medical Research Council (NMRC) NMRC/MOHIAFCAT2/006/2016Singapore National Medical Research Council (NMRC) NRF-CRP17-2017-05
6 · The paper itself

Abstract

The fibroblast growth factor (FGF) signaling cascade is a key signaling pathway in hepatocarcinogenesis. We report high FGF receptor (FGFR) expression in 17.7% (11 of 62) of hepatocellular carcinoma (HCC) models. Infigratinib, a pan-FGFR inhibitor, potently suppresses the growth of high-FGFR-expressing and sorafenib-resistant HCCs. Infigratinib inhibits FGFR signaling and its downstream targets, cell proliferation, the angiogenic rescue program, hypoxia, invasion, and metastasis. Infigratinib also induces apoptosis and vessel normalization and improves the overall survival of mice bearing FGFR-driven HCCs. Infigratinib acts in synergy with the microtubule-depolymerizing drug vinorelbine to promote apoptosis, suppress tumor growth, and improve the overall survival of mice. Increased expression levels of FGFR-2 and FGFR-3 through gene amplification correlate with treatment response and may serve as potential biomarkers for patient selection. Conclusion: Treatments with Infigratinib alone or in combination with vinorelbine may be effective in a subset of patients with HCC with FGFR-driven tumors.

Indexed as

AnimalsBlood VesselsCarcinoma, HepatocellularLiver NeoplasmsMaleMiceMice, SCIDPhenylurea CompoundsPyrimidinesinfigratinibPhenylurea CompoundsPyrimidines

Identifiers

PMID30575985
PMCPMC6635738

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.