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

Author:

Orlandi Elena1ORCID,Guasconi Massimo23ORCID,Vecchia Stefano4ORCID,Trubini Serena1,Giuffrida Mario5ORCID,Proietto Manuela1,Anselmi Elisa1,Capelli Patrizio5ORCID,Romboli Andrea5ORCID

Affiliation:

1. Department of Oncology-Hematology, Azienda USL of Piacenza, 29121 Piacenza, Italy

2. Department of Medicine and Surgery, University of Parma, 43121 Parma, Italy

3. Department of Health Professions Management, Azienda USL of Piacenza, 29121 Piacenza, Italy

4. Department of Pharmacy, Azienda USL of Piacenza, 29121 Piacenza, Italy

5. Department of General Surgery, Azienda USL of Piacenza, 29121 Piacenza, Italy

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.

Publisher

MDPI AG

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