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Updated: Mar 11, 2026

Testing Targeted Therapies in Cancer using Structural DNA Alteration Analysis and Patient-Derived Xenografts
Published on: July 25, 2020
[Cutaneous side effects of targeted cancer drugs]
J Below1, B Homey1, P A Gerber2
1Klinik für Dermatologie, Universitätsklinikum Düsseldorf, Moorenstr. 5, 40225, Düsseldorf, Deutschland.
Abstract:
In the past decades many new drugs were approved for the treatment of cancer and have been established as essential parts of various therapeutic regimens. In particular targeted therapies and immune checkpoint inhibitors that aim at specific carcinogenic signaling pathways or modulate the tumor-immune response have revolutionized cancer therapy. Despite their targeted actions, these drugs may lead to diverse adverse reactions. In particular, cutaneous toxicities represent a serious threat to patients' quality of life and may lead to dose reduction or therapy cessation. In most cases, basic management is performed by the treating oncologist. Nevertheless, more severe reactions may require the expertise of a dermatologist. In this review, we present specific cutaneous adverse reactions of new drug classes such as epidermal growth factor receptor inhibitors (EGFR-I), multikinase inhibitors (MKI), BRAF inhibitors, MEK inhibitors, and immune checkpoint inhibitors (anti-PD1-, anti-CTLA4-antibodies). Furthermore, we give recommendations concerning the prevention and management of respective cutaneous reactions.
Insights
New cancer therapies like targeted therapies and immune checkpoint inhibitors can cause skin side effects. This review details these adverse reactions and provides management recommendations for oncologists and dermatologists.
Area of Science:
- Oncology
- Dermatology
- Pharmacology
Background:
- Cancer therapeutics have advanced with targeted therapies and immune checkpoint inhibitors.
- These novel drugs, while effective, can cause significant adverse reactions, particularly cutaneous toxicities.
- Skin toxicities impact patient quality of life and may necessitate treatment modification.
Purpose of the Study:
- To review the spectrum of cutaneous adverse reactions associated with new cancer drug classes.
- To provide management and prevention strategies for these drug-induced skin toxicities.
- To guide oncologists and dermatologists in managing dermatologic side effects of cancer therapy.
Main Methods:
- Literature review of cutaneous adverse events linked to specific cancer drug classes.
- Analysis of mechanisms underlying drug-induced dermatologic toxicities.
- Synthesis of current recommendations for prevention and management.
Main Results:
- Detailed descriptions of skin toxicities from epidermal growth factor receptor inhibitors (EGFR-I), multikinase inhibitors (MKI), BRAF inhibitors, MEK inhibitors, and immune checkpoint inhibitors (anti-PD1, anti-CTLA4).
- Identification of common and severe cutaneous reactions.
- Emphasis on the need for multidisciplinary management involving dermatologists.
Conclusions:
- Cutaneous toxicities are common and impactful side effects of modern cancer therapies.
- Early recognition and appropriate management are crucial for patient quality of life and treatment adherence.
- This review offers a practical guide for managing these adverse events.
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