Evidence map›Paper›PMID 39590169›Full record

ArticleCurrent oncology (Toronto, Ont.)2024

Novel Fibroblast Growth Factor Receptor 3-Fatty Acid Synthase Gene Fusion in Recurrent Epithelioid Glioblastoma Linked to Aggressive Clinical Progression.

Miguel A Diaz, Felisa Vázquez-Gómez, Irene Garrido, Francisco Arias, Julia Suarez, Ismael Buño, Álvaro Lassaletta

Abstract readCase Reports
In one paragraph

Article in Current oncology (Toronto, Ont.), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
–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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Miguel A DiazPediatric Hematology/Oncology, Hospital Infantil Universitario "Niño Jesús", Universidad Autónoma de Madrid, 28009 Madrid, Spain.
Felisa Vázquez-GómezPediatric Hematology/Oncology, Hospital Infantil Universitario "Niño Jesús", Universidad Autónoma de Madrid, 28009 Madrid, Spain.ORCID 0000-0003-3100-9561
Irene GarridoNeuro-Radiology, Hospital General Universitario "Gregorio Marañón", 28007 Madrid, Spain.
Francisco AriasPathology Department, Hospital General Universitario "Gregorio Marañón", 28007 Madrid, Spain.
Julia SuarezGenomics Unit, Hospital General Universitario "Gregorio Marañón", 28007 Madrid, Spain.ORCID 0000-0002-4778-7096
Ismael BuñoGenomics Unit, Hospital General Universitario "Gregorio Marañón", 28007 Madrid, Spain.ORCID 0000-0003-4931-9170
Álvaro LassalettaPediatric Hematology/Oncology, Hospital Infantil Universitario "Niño Jesús", Universidad Autónoma de Madrid, 28009 Madrid, Spain.ORCID 0000-0003-2881-1473

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glioblastoma (GBM) is the most common primary malignant brain tumor in adults, with a median overall survival (OS) of 15-18 months despite standard treatments. Approximately 8% of GBM cases exhibit genomic alterations in fibroblast growth factor receptors (FGFRs), particularly FGFR1 and FGFR3. Next-generation sequencing techniques have identified various FGFR3 fusions in GBM. This report presents a novel FGFR3 fusion with fatty acid synthase (FASN) in a 41-year-old male diagnosed with GBM. The patient presented with a persistent headache, and imaging revealed a right frontal lobe lesion. Surgical resection and subsequent histopathology confirmed GBM. Initial NGS analysis showed no mutations in the IDH1, IDH2 or H3F3 genes, but revealed a TERT promoter mutation and CDKN2A/2B and PTEN deletions. Postoperative treatment included radiotherapy and temozolomide. Despite initial management, recurrence occurred four months post-diagnosis, confirmed by MRI and histology. A second surgery identified a novel FGFR3-FASN fusion, alongside increased Ki67 expression. The recurrence was managed with regorafenib and bevacizumab, though complications like hand-foot syndrome and radiation necrosis arose. Despite initial improvement, the patient died 15 months after diagnosis. This case underscores the importance of understanding GBM's molecular landscape for effective treatment strategies. The novel FGFR3-FASN fusion suggests potential implications for GBM recurrence and lipid metabolism. Further studies are warranted to explore FGFR3-FASN's role in GBM and its therapeutic targeting.

Indexed as

Brain NeoplasmsGlioblastomaReceptor, Fibroblast Growth Factor, Type 3AdultDisease ProgressionFatty Acid SynthasesFatty Acid Synthase, Type IGene FusionHumansMaleNeoplasm Recurrence, LocalFASN protein, humanFatty Acid SynthasesFatty Acid Synthase, Type IFGFR3 protein, humanReceptor, Fibroblast Growth Factor, Type 3epithelioidFASNfatty acidFGFR3fusionglioblastomapseudoprogressionradionecrosis

Identifiers

PMID39590169
PMCPMC11592913

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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.