Targeted agents: management of dermatologic toxicities

Barbara Burtness1

  • 1Presented by Barbara Burtness, MD, Clinical Research Program Leader of the Head and Neck Cancers Program, Smilow Cancer Hospital at Yale-New Haven, and Co-Director, Developmental Therapeutics Research Program, Yale Cancer Center.

Insights

Targeted cancer therapies like epidermal growth factor receptor (EGFR) inhibitors can cause prominent skin side effects. Management focuses on improving these cutaneous complications to maintain anticancer treatment.

Area of Science:

  • Oncology
  • Dermatology
  • Pharmacology

Background:

  • Targeted cancer therapies, including epidermal growth factor receptor (EGFR) inhibitors, BRAF, and mTOR inhibitors, are associated with significant cutaneous toxicity.
  • Dermatologic side effects are a common and prominent concern in patients undergoing treatment with these agents.

Discussion:

  • Dr. Barbara Burtness highlighted common skin complications from targeted therapies at the NCCN 19th Annual Conference.
  • Strategies for managing skin toxicities include prophylactic and reactive approaches, emphasizing local measures for quality of life.
  • Key interventions involve topical and oral antibiotics and topical steroids to address infections and cosmetic issues.

Key Insights:

  • Cutaneous toxicities from targeted therapies require proactive and reactive management strategies.
  • Improving skin complications is crucial for patient quality of life and adherence to cancer treatment.
  • Early intervention with antibiotics and steroids can effectively manage common dermatologic side effects.

Outlook:

  • Further research into optimizing the management of therapy-induced skin conditions is warranted.
  • Developing standardized protocols for managing cutaneous side effects can improve patient outcomes.
  • Continued focus on supportive care is essential to minimize treatment interruptions due to skin toxicity.

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