Related Experiment Video
Updated: Jul 10, 2026

Murine Model of Epicutaneously-Induced Immunomodulation
Published on: June 24, 2025
Cutaneous reactions related to systemic immunomodulators and targeted therapeutics
16126 Amble Trail, San Antonio, TX 78249, USA. lisa.hammond-md@satx.rr.com
Abstract:
The arrival of targeted therapeutics into the oncology clinic, while enthusiastically anticipated, introduced the oncologist to dermatologic events that can pose challenging management issues. The dermatologic effects of these targeted agents appear to be more frequent than those with cytotoxic therapy and are not uniform; that is, different agents have distinct dermatologic toxicities. Interestingly, dermatologic toxicity may correlate with antitumor activity with some of these targeted agents. The correlation of rash with response and survival in particular mandates the development of effective and appropriate management strategies. The nature and challenges of the dermatologic events observed to date with epidermal growth factor receptor inhibitors, multikinase inhibitors, proteosome inhibitors, BCR-ABL tyrosine kinase inhibitors, and immunomodulatory drugs will be addressed in this review.
Insights
Targeted cancer therapies cause unique skin toxicities more often than traditional chemotherapy. Managing these dermatologic side effects is crucial, as rash may indicate treatment effectiveness.
Area of Science:
- Oncology
- Dermatology
- Pharmacology
Background:
- Targeted therapeutics have revolutionized cancer treatment.
- These novel agents are associated with distinct and frequent dermatologic toxicities.
- Understanding these side effects is essential for patient management.
Purpose of the Study:
- To review the dermatologic events associated with targeted cancer therapies.
- To discuss the challenges in managing these toxicities.
- To explore the correlation between dermatologic toxicity and therapeutic efficacy.
Main Methods:
- Literature review of dermatologic events from targeted agents.
- Analysis of specific drug classes including epidermal growth factor receptor inhibitors, multikinase inhibitors, proteasome inhibitors, BCR-ABL tyrosine kinase inhibitors, and immunomodulatory drugs.
- Discussion of management strategies and correlation with clinical outcomes.
Main Results:
- Dermatologic toxicities from targeted agents are common and varied.
- Different targeted therapies present unique skin manifestations.
- Dermatologic adverse events, particularly rash, may correlate with antitumor activity, response, and survival.
Conclusions:
- Effective management strategies for targeted therapy-induced dermatologic events are necessary.
- The correlation between rash and efficacy highlights the importance of monitoring and supportive care.
- This review provides insights into managing skin toxicities for improved patient outcomes in oncology.
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