Evidence map›Paper›PMID 30181810›Full record

ArticleOncotarget2018

FGFR3 mRNA overexpression defines a subset of oligometastatic colorectal cancers with worse prognosis.

Julia Elisabeth Fromme, Katja Schmitz, Astrid Wachter, Marius Grzelinski, Dirk Zielinski, Christina Koppel, Lena-Christin Conradi, Kia Homayounfar, Tabea Hugo, Sara Hugo and 8 more

Abstract read
In one paragraph

Article in Oncotarget, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing 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

17 citing papers in PubMed.

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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

18 authors.

Julia Elisabeth FrommeInstitute of Pathology, University Hospital Göttingen, Göttingen, Germany.
Katja SchmitzInstitute of Pathology, University Hospital Göttingen, Göttingen, Germany.
Astrid WachterDepartment of Medical Statistics, University Medical Center Göttingen, Göttingen, Germany.
Marius GrzelinskiTargos Molecular Pathology Inc., Kassel, Germany.
Dirk ZielinskiTargos Molecular Pathology Inc., Kassel, Germany.
Christina KoppelTargos Molecular Pathology Inc., Kassel, Germany.
Lena-Christin ConradiDepartment of General, Visceral and Pediatric Surgery, University Medical Center Göttingen, Georg-August-University, Goettingen, Germany.
Kia HomayounfarDepartment of General, Visceral and Pediatric Surgery, University Medical Center Göttingen, Georg-August-University, Goettingen, Germany.
Tabea HugoInstitute of Pathology, University Hospital Göttingen, Göttingen, Germany.
Sara HugoInstitute of Pathology, University Hospital Göttingen, Göttingen, Germany.
Laura LukatInstitute of Pathology, University Hospital Göttingen, Göttingen, Germany.
Josef RüschoffTargos Molecular Pathology Inc., Kassel, Germany.
Philipp StröbelInstitute of Pathology, University Hospital Göttingen, Göttingen, Germany.
Michael GhadimiDepartment of General, Visceral and Pediatric Surgery, University Medical Center Göttingen, Georg-August-University, Goettingen, Germany.
Tim BeißbarthDepartment of Medical Statistics, University Medical Center Göttingen, Göttingen, Germany.
Kirsten Reuter-JessenInstitute of Pathology, University Hospital Göttingen, Göttingen, Germany.
Annalen BleckmannDepartment of Medical Statistics, University Medical Center Göttingen, Göttingen, Germany.
Hans-Ulrich SchildhausInstitute of Pathology, University Hospital Göttingen, Göttingen, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesMetastatic colorectal cancer (CRC) remains a leading cause of cancer related deaths. Patients with oligometastatic liver disease represent a clinical subgroup with heterogeneous course. Until now, biomarkers to characterize outcome and therapeutic options have not been fully established.

methodsWe investigated the prevalence of FGFR alterations in a total of 140 primary colorectal tumors and 63 liver metastases of 55 oligometastatic CRC patients. FGF receptors (

resultsPrimary tumors showed

conclusionsWe provide the so far most comprehensive analysis of FGFR alterations in primary and metastatic CRC. We describe FGFR3 overexpression in 15% of CRC patients with oligometastatic liver disease as a prognosticator for poor outcome. Recently FGFR3 overexpression has been shown to be a potential therapeutic target. Therefore, we suggest focusing on this subgroup in upcoming clinical trials with FGFR-targeted therapies.

Indexed as

colorectal cancerFGFR3fibroblast growth factor receptorsmetastasesRNA in situ hybridization

Identifiers

PMID30181810
PMCPMC6114946

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Registered trials

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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.