Evidence map›Paper›PMID 39199681›Full record

ArticleCancers2024

Exploring the Horizon: Anti-Fibroblast Growth Factor Receptor Therapy in Pancreatic Cancer with Aberrant Fibroblast Growth Factor Receptor Expression-A Scoping Review.

Elena Orlandi, Massimo Guasconi, Stefano Vecchia, Serena Trubini, Mario Giuffrida, Manuela Proietto, Elisa Anselmi, Patrizio Capelli, Andrea Romboli

Abstract readScoping Review
In one paragraph

Article in Cancers, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Elena OrlandiDepartment of Oncology-Hematology, Azienda USL of Piacenza, 29121 Piacenza, Italy.ORCID 0000-0002-2559-7558
Massimo GuasconiDepartment of Medicine and Surgery, University of Parma, 43121 Parma, Italy.ORCID 0000-0002-8855-8919
Stefano VecchiaDepartment of Pharmacy, Azienda USL of Piacenza, 29121 Piacenza, Italy.ORCID 0000-0003-0578-0870
Serena TrubiniDepartment of Oncology-Hematology, Azienda USL of Piacenza, 29121 Piacenza, Italy.
Mario GiuffridaDepartment of General Surgery, Azienda USL of Piacenza, 29121 Piacenza, Italy.ORCID 0000-0001-8335-3941
Manuela ProiettoDepartment of Oncology-Hematology, Azienda USL of Piacenza, 29121 Piacenza, Italy.
Elisa AnselmiDepartment of Oncology-Hematology, Azienda USL of Piacenza, 29121 Piacenza, Italy.
Patrizio CapelliDepartment of General Surgery, Azienda USL of Piacenza, 29121 Piacenza, Italy.ORCID 0000-0001-9434-3984
Andrea RomboliDepartment of General Surgery, Azienda USL of Piacenza, 29121 Piacenza, Italy.ORCID 0000-0002-7725-635X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pancreatic cancer is a highly lethal disease, often diagnosed at advanced stages, with a 5-year overall survival rate of around 10%. Current treatments have limited effectiveness, underscoring the need for new therapeutic options. This scoping review aims to identify and summarize preclinical and clinical studies on FGFR (Fibroblast Growth Factor Receptor) inhibitors, including tyrosine kinase inhibitors (TKIs) and FGFR-specific inhibitors, in pancreatic cancer with FGFR alterations. We included studies analyzing efficacy, safety, and survival outcomes in various populations. A comprehensive search across major databases identified 73 relevant studies: 32 preclinical, 16 clinical, and 25 from gray literature. The clinical trials focused primarily on efficacy (20 studies) and safety (14 studies), with fewer studies addressing survival outcomes. FGFR1 was the most studied alteration, followed by FGFR2 and FGFR4. Although FGFR alterations are relatively rare in pancreatic cancer, the available data, including promising real-life outcomes, suggest significant potential for FGFR inhibitors. However, more extensive research is needed to identify the correct genetic drivers and gather robust survival data. Ongoing and future trials are expected to provide more comprehensive insights, potentially leading to improved targeted therapies for pancreatic cancer patients with FGFR alterations.

Indexed as

FGFRFGFR alterationpancreatic cancerscoping reviewtarget therapy

Identifiers

PMID39199681
PMCPMC11352631

What OpenQuestion holds

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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.