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Updated: May 24, 2026

Testing Targeted Therapies in Cancer using Structural DNA Alteration Analysis and Patient-Derived Xenografts
Published on: July 25, 2020
[Skin manifestations of new targeted treatments]
M Hello1, S Barbarot, J Connault
1Service de médecine interne, CHU Hôtel-Dieu, Nantes, France. muriel.hello@chu-nantes.fr
Abstract:
Many cutaneous adverse events have been identified with recently developed targeted treatments. Some of them are common and specific, like paradoxical psoriasiform eruptions with anti-TNFα, papulopustular eruptions and paronychias with EGFR inhibitors and peculiar hand-foot skin reactions with multitargeted kinase inhibitors sorefenib and sunitinib. Patients treated with these recently available biologics need a careful monitoring.
Insights
Targeted cancer therapies can cause specific skin side effects. Careful patient monitoring is crucial for managing these common cutaneous adverse events associated with new biologic treatments.
Area of Science:
- Dermatology
- Oncology
- Pharmacology
Background:
- Targeted therapies represent a significant advancement in cancer treatment.
- These novel therapies are associated with a range of cutaneous adverse events.
- Understanding these specific dermatologic toxicities is essential for patient management.
Purpose of the Study:
- To review and summarize common and specific cutaneous adverse events linked to emerging targeted cancer treatments.
- To highlight the importance of monitoring patients undergoing these therapies.
Main Methods:
- Literature review of recently developed targeted treatments and their associated skin reactions.
- Categorization of adverse events based on drug class and mechanism of action.
Main Results:
- Anti-tumor necrosis factor-alpha (anti-TNFα) therapies are linked to paradoxical psoriasiform eruptions.
- Epidermal growth factor receptor (EGFR) inhibitors can cause papulopustular eruptions and paronychias.
- Multitargeted kinase inhibitors, such as sorafenib and sunitinib, are associated with hand-foot skin reactions.
Conclusions:
- Specific cutaneous adverse events are characteristic of particular targeted therapies.
- Vigilant dermatological monitoring is necessary for patients receiving these advanced biologic treatments.
- Proactive management of skin toxicities can improve patient outcomes and treatment adherence.
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