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Updated: Dec 12, 2025
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Automated Preparation of [68Ga]Ga-3BP-3940 on a Synthesis Module for PET Imaging of the Tumor Microenvironment
Published on: April 25, 2025
Therapeutic implications of fibroblast growth factor receptor inhibitors in a combination regimen for solid tumors
Hong Luo1, Tao Zhang1, Peng Cheng1
1Department of Oncology, General Hospital of Western Theater Command, Chengdu, Sichuan 610083, P.R. China.
Abstract:
A number of novel drugs targeting the fibroblast growth factor receptor (FGFR) signaling pathway have been developed, including mostly tyrosine kinase inhibitors, selective inhibitors or monoclonal antibodies. Multiple preclinical and clinical studies have been conducted worldwide to ascertain their effects on diverse solid tumors. Drugs, such as lenvatinib, dovitinib and other non-specific FGFR inhibitors, widely used in clinical practice, have been approved by the Food and Drug Administration for cancer therapy, although the majority of drugs remain in preclinical tests or clinical research. The resistance to a single agent for FGFR inhibition with synthetic lethal action may be overcome by a combination of therapeutic approaches and FGFR inhibitors, which could also enhance the sensitivity to other therapeutics. Therefore, the aim of the present review is to describe the pharmacological characteristics of FGFR inhibitors that may be combined with other therapeutic agents and the preclinical data supporting their combination. Additionally, their clinical implications and the remaining challenges for FGFR inhibitor combination regimens are discussed.
Insights
Novel fibroblast growth factor receptor (FGFR) inhibitors show promise for cancer therapy. Combining FGFR inhibitors with other treatments may overcome resistance and improve effectiveness in solid tumors.
Area of Science:
- Oncology
- Pharmacology
Background:
- Fibroblast growth factor receptor (FGFR) signaling pathway is a target for novel cancer drugs.
- Approved FGFR inhibitors like lenvatinib and dovitinib are used in clinical practice for cancer therapy.
- Many FGFR inhibitors are still in preclinical or clinical research stages.
Purpose of the Study:
- To review the pharmacological characteristics of FGFR inhibitors for combination therapy.
- To present preclinical data supporting the use of FGFR inhibitors in combination regimens.
- To discuss clinical implications and challenges of FGFR inhibitor combination strategies.
Main Methods:
- Literature review of preclinical and clinical studies on FGFR inhibitors.
- Analysis of pharmacological properties of various FGFR inhibitors.
- Evaluation of data supporting combination therapies involving FGFR inhibitors.
Main Results:
- FGFR inhibitors, including tyrosine kinase inhibitors, selective inhibitors, and monoclonal antibodies, are being developed.
- Combination of FGFR inhibitors with other therapeutic agents may overcome resistance and enhance sensitivity.
- Approved non-specific FGFR inhibitors are available, but most novel agents are in research phases.
Conclusions:
- Combination regimens involving FGFR inhibitors hold potential for enhanced cancer treatment.
- Further research is needed to address clinical implications and challenges for combination therapies.
- Optimizing FGFR inhibitor combinations could improve outcomes for diverse solid tumors.
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