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Dermatologic Toxicities of Targeted Therapy and Immunotherapy in Head and Neck Cancers
Maria L Espinosa1, Chelsea Abad2, Yaira Kurtzman2
1Department of Dermatology, University of Chicago Pritzker School of Medicine, Chicago, IL, United States.
Abstract:
Treatment of head and neck cancers requires multidisciplinary collaboration to reduce morbidity and mortality associated with the tumor burden, as well as to preserve function of organs and structures. With the use of various new targeted therapies come new adverse events including dermatologic toxicities, which may consist of xerosis, nail and hair changes, morbilliform or papulopustular rashes, to more severe eruptions such as Stevens-Johnson syndrome. We describe the dermatologic toxicities and corresponding grades of severity and associated pathophysiology resulting from seven therapeutics used to treat head and neck cancers: cetuximab, trastuzumab, pembrolizumab, nivolumab, lentatinib, larotrectinib, and entrectinib. Being familiar with these dermatologic toxicities allows clinicians to provide comprehensive counseling for patients, encourage preventative measures, and to know when it is appropriate to hold therapy or permanently stop treatment.
Insights
New targeted therapies for head and neck cancers can cause various skin side effects, from dryness to severe rashes. Understanding these dermatologic toxicities helps clinicians manage patient care and treatment decisions.
Area of Science:
- Oncology
- Dermatology
- Pharmacology
Background:
- Head and neck cancer treatment involves multidisciplinary collaboration to manage tumor burden and preserve organ function.
- Emerging targeted therapies introduce novel adverse events, particularly dermatologic toxicities.
- These toxicities range from mild xerosis and rash to severe conditions like Stevens-Johnson syndrome.
Purpose of the Study:
- To describe the dermatologic toxicities associated with seven targeted therapeutics used in head and neck cancer treatment.
- To detail the grades of severity and underlying pathophysiology of these skin-related adverse events.
- To equip clinicians with knowledge for comprehensive patient counseling and treatment management.
Main Methods:
- Review and synthesis of literature on dermatologic toxicities.
- Categorization of toxicities by drug and severity grade.
- Description of the pathophysiology for each drug-induced dermatologic event.
Main Results:
- Seven targeted therapeutics (cetuximab, trastuzumab, pembrolizumab, nivolumab, lentatinib, larotrectinib, entrectinib) were analyzed.
- Dermatologic toxicities include xerosis, nail/hair changes, various rashes, and severe eruptions.
- Pathophysiology and grading of severity for each drug's associated skin toxicities were detailed.
Conclusions:
- Clinicians must be familiar with the spectrum of dermatologic toxicities from targeted head and neck cancer therapies.
- Knowledge of these toxicities facilitates patient counseling, preventative strategies, and informed treatment adjustments (holding or stopping therapy).
- Proactive management of dermatologic adverse events is crucial for optimizing patient outcomes and treatment adherence.
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