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Published on: July 25, 2020
Cutaneous adverse reactions resulting from targeted cancer therapies: histopathologic and clinical findings
Dylan Haynes1, Eric E Morgan2, Emily Y Chu1
1Department of Dermatology, Hospital of the University of Pennsylvania, Philadelphia, PA, 19104, USA.
Abstract:
Targeted cancer treatments-designed to interfere with specific molecular signals responsible for tumor survival and progression-have shown benefit over conventional chemotherapies but may lead to diverse cutaneous adverse effects. This review highlights clinically significant dermatologic toxicities and their associated histopathologic findings, resulting from various targeted cancer drugs. Case reports and series, clinical trials, reviews, and meta-analyses are included for analysis and summarized herein. Cutaneous side effects resulting from targeted cancer therapies were reported with incidences as high as 90% for certain medications, and reactions are often predictable based on mechanism(s) of action of a given drug. Common and important reaction patterns included: acneiform eruptions, neutrophilic dermatoses, hand-foot skin reaction, secondary cutaneous malignancies, and alopecia. Clinical and histopathologic recognition of these toxicities remains impactful for patient care.
Insights
Targeted cancer therapies can cause significant skin side effects, with some reactions occurring in up to 90% of patients. Recognizing these predictable dermatologic toxicities is crucial for effective patient care.
Area of Science:
- Oncology
- Dermatology
- Pharmacology
Background:
- Targeted cancer treatments offer an alternative to conventional chemotherapy by interfering with specific molecular pathways.
- While effective, these therapies are associated with a range of adverse cutaneous effects.
- Understanding these dermatologic toxicities is essential for managing patients undergoing targeted cancer therapy.
Purpose of the Study:
- To review and summarize clinically significant dermatologic toxicities associated with targeted cancer drugs.
- To correlate these toxicities with their underlying histopathologic findings.
- To provide a comprehensive overview of predictable cutaneous reactions based on drug mechanisms.
Main Methods:
- Systematic review of case reports and series, clinical trials, reviews, and meta-analyses.
- Analysis and summarization of reported dermatologic side effects and their histopathologic features.
- Focus on common and significant reaction patterns observed with targeted cancer therapies.
Main Results:
- Cutaneous side effects from targeted cancer therapies can occur with incidences as high as 90%.
- Common reaction patterns include acneiform eruptions, neutrophilic dermatoses, hand-foot skin reactions, secondary cutaneous malignancies, and alopecia.
- Many adverse skin reactions are predictable based on the drug's mechanism of action.
Conclusions:
- Targeted cancer therapies frequently cause diverse and predictable dermatologic toxicities.
- Clinical and histopathologic recognition of these side effects is vital for optimal patient management.
- This review underscores the importance of dermatologic monitoring in patients receiving targeted cancer treatments.
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