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Updated: May 28, 2026

Monitoring Functionality and Morphology of Vasculature Recruited by Factors Secreted by Fast-growing Tumor-generating Cells
Published on: November 23, 2014
[Dermatologic side effects induced by new angiogenesis inhibitors]
Vincent Sibaud1, Ignacio Garrido-Stowhas, Ewa Cottura
1Institut Claudius-Regaud, Toulouse cedex, France. sibaud.vincent@claudiusregaud.fr
New anticancer angiogenesis inhibitors, while generally safe, can cause skin and hair toxicities. This review details the dermatologic adverse events associated with targeted therapies like sorafenib and bevacizumab.
Area of Science:
- Oncology
- Dermatology
- Pharmacology
Background:
- Targeted anticancer therapies often possess antiangiogenic activity.
- These drugs target signaling pathways and receptors crucial for skin and hair follicle physiology.
- Cutaneous toxicity is a significant concern with these novel agents.
Purpose of the Study:
- To review the primary dermatologic adverse events associated with antiangiogenic targeted therapies.
- To provide an overview of skin and hair-related toxicities induced by specific anticancer drugs.
Main Methods:
- Literature review of dermatologic adverse events.
- Analysis of side effect profiles for key antiangiogenic drugs.
- Synthesis of information on cutaneous toxicities.
Main Results:
- Common dermatologic adverse events include rash, hand-foot syndrome, and hair changes.
- Specific drugs like sorafenib, sunitinib, pazopanib, vandetanib, everolimus, temsirolimus, and bevacizumab are associated with distinct cutaneous toxicities.
- The physiological expression of targeted pathways in the skin contributes to these side effects.
Conclusions:
- Antiangiogenic targeted therapies, despite a favorable safety profile, frequently cause dermatologic adverse events.
- Understanding and managing these cutaneous toxicities is essential for patient care.
- Further research into mitigating these side effects is warranted.
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