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Published on: May 7, 2019
Dermatologic Adverse Events Associated with Selective Fibroblast Growth Factor Receptor Inhibitors: Overview,
Mario E Lacouture1, Vincent Sibaud2, Milan J Anadkat3
1Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Abstract:
Fibroblast growth factor receptor (FGFR) tyrosine kinases, which are expressed on the cell membrane, are involved in a wide range of biological functions such as cell proliferation, survival, migration, and differentiation. The identification of FGFR fusions and other alterations in a wide range of solid tumors, including cholangiocarcinoma and bladder cancer, has resulted in the development of several selective FGFR inhibitors for use in these indications, for example, infigratinib, erdafitinib, derazantinib, pemigatinib, and futibatinib. In addition to the typical adverse events associated with tyrosine kinases, the FGFR inhibitors appear to give rise to a number of adverse events affecting the skin. Here we describe these skin events, which include the more common nail adverse events (e.g., onycholysis), palmar-plantar erythrodysesthesia syndrome, and stomatitis, as well as less common reactions such as calciphylaxis. This review aims to provide oncologists with an understanding of these dermatologic events and proposes guidelines for the management of treatment-emergent dermatologic adverse events. Awareness of possible adverse events associated with specific drugs should allow physicians to educate patients as to what to expect and implement effective management plans at the earliest possible opportunity, thereby preventing premature discontinuation while maintaining patient quality of life. IMPLICATIONS FOR PRACTICE: Identification of fibroblast growth factor receptor (FGFR) aberrations in cholangiocarcinoma and bladder cancer led to development of selective FGFR inhibitors for these indications, based on clinical benefit and safety profiles. The most frequent adverse events (AEs) include those affecting skin, hair, and nails, a unique class effect of these agents. These are usually mild to moderate in severity. This work reviewed skin AEs reported with FGFR inhibitors and provides management guidelines for physicians, aiming to increase awareness of skin events and provide effective treatment strategies. Early intervention and effective management may improve treatment adherence, optimize outcomes, and improve quality of life.
Insights
Fibroblast growth factor receptor (FGFR) inhibitors are used for cancers like cholangiocarcinoma and bladder cancer. These drugs can cause skin, hair, and nail side effects, requiring physician awareness and management strategies for better patient outcomes.
Area of Science:
- Oncology
- Dermatology
- Pharmacology
Background:
- Fibroblast growth factor receptor (FGFR) tyrosine kinases regulate cell functions and are implicated in various solid tumors.
- FGFR alterations in cholangiocarcinoma and bladder cancer have led to the development of targeted therapies, including selective FGFR inhibitors.
- These inhibitors, while effective, are associated with unique adverse events, particularly dermatologic toxicities.
Purpose of the Study:
- To review and describe the spectrum of skin-related adverse events associated with FGFR inhibitors.
- To provide oncologists with practical guidelines for managing treatment-emergent dermatologic adverse events.
- To enhance physician and patient understanding of potential side effects to ensure treatment adherence and maintain quality of life.
Main Methods:
- Literature review of adverse events reported with FGFR inhibitors (infigratinib, erdafitinib, derazantinib, pemigatinib, futibatinib).
- Analysis of common and less common dermatologic reactions, including nail changes, palmar-plantar erythrodysesthesia, stomatitis, and calciphylaxis.
- Development of evidence-based management strategies and recommendations for oncologists.
Main Results:
- FGFR inhibitors commonly cause skin, hair, and nail adverse events, which are generally mild to moderate.
- Specific dermatologic toxicities include onycholysis, palmar-plantar erythrodysesthesia syndrome, stomatitis, and rarely, calciphylaxis.
- These events are considered a class effect of FGFR inhibitors.
Conclusions:
- Awareness of FGFR inhibitor-associated dermatologic adverse events is crucial for oncologists.
- Effective management strategies can mitigate side effects, prevent treatment discontinuation, and improve patient quality of life.
- Early recognition and intervention are key to optimizing treatment adherence and outcomes in patients receiving FGFR inhibitors.
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