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Screening and Identification of Small Peptides Targeting Fibroblast Growth Factor Receptor2 using a Phage Display Peptide Library
Published on: September 30, 2019
Fibroblast growth factor receptor inhibitor-induced hyperphosphatemia: Lessons for the nephrologist
Introduction:
Fibroblast growth factor inhibitors (FGFRi) are novel cancer drugs that offer new hope for patients with advanced biliary tract cancers and metastatic urothelial tumors. Despite their effectiveness, they often cause hyperphosphatemia.
Materials And Methods:
We investigated the incidence and characteristics of hyperphosphatemia in patients treated with FGFRi at Northwell Health, comparing findings with clinical trials and the FDA Adverse Event Reporting System database.
Results:
94% of patients in our series developed hyperphosphatemia, predominantly grade 2. The time-to-onset of hyperphosphatemia was longer than noted in clinical trials. Patients on erdafitinib showed a higher-than-expected incidence and grade of hyperphosphatemia.
Conclusion:
Collaboration between nephrologists and oncologists is crucial for optimizing treatment benefits and managing side effects. Further research is warranted to refine management strategies and to understand the clinical implications of hyperphosphatemia.
Insights
Fibroblast growth factor receptor inhibitors (FGFRi) commonly cause hyperphosphatemia in cancer patients. This study found a high incidence of hyperphosphatemia, emphasizing the need for collaborative management between nephrologists and oncologists.
Area of Science:
- Oncology
- Nephrology
- Pharmacology
Background:
- Fibroblast growth factor receptor inhibitors (FGFRi) represent a novel class of targeted cancer therapies.
- These drugs show promise for advanced biliary tract cancers and metastatic urothelial tumors.
- Hyperphosphatemia is a frequent adverse effect associated with FGFRi treatment.
Purpose of the Study:
- To investigate the incidence and clinical characteristics of hyperphosphatemia in patients receiving FGFRi.
- To compare real-world data with findings from clinical trials and the FDA Adverse Event Reporting System.
- To highlight the importance of multidisciplinary care in managing FGFRi-induced hyperphosphatemia.
Main Methods:
- Retrospective analysis of patients treated with FGFRi at Northwell Health.
- Comparison of observed hyperphosphatemia rates and characteristics against published clinical trial data.
- Review of the FDA Adverse Event Reporting System (FAERS) database for FGFRi-related events.
Main Results:
- A high incidence of hyperphosphatemia (94%) was observed in the study cohort, predominantly Grade 2.
- The time to onset of hyperphosphatemia was longer than reported in clinical trials.
- Patients treated with erdafitinib exhibited a higher incidence and grade of hyperphosphatemia than anticipated.
Conclusions:
- Close collaboration between nephrologists and oncologists is essential for optimizing FGFRi therapy and managing side effects.
- Further research is needed to establish refined management strategies for FGFRi-induced hyperphosphatemia.
- Understanding the clinical implications of hyperphosphatemia is crucial for improving patient outcomes.
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