Dermatologic toxicities of antibody-drug conjugates

Christian Gronbeck1, Matthew J Hadfield2, Jane M Grant-Kels3

  • 1Department of Dermatology, University of Connecticut Health Center, Farmington, Connecticut.

Insights

Antibody-drug conjugates (ADCs) offer targeted cancer therapy but can cause unique skin toxicities. Dermatologists must recognize and manage these side effects to ensure patient safety and treatment adherence.

Area of Science:

  • Oncology
  • Dermatology
  • Pharmacology

Background:

  • Antibody-drug conjugates (ADCs) represent an emerging class of cancer therapeutics.
  • ADCs combine monoclonal antibodies for targeted delivery with cytotoxic payloads.
  • Over 80 ADCs are in clinical development, highlighting their growing importance.

Purpose of the Study:

  • To review the mechanisms and indications of approved ADCs.
  • To summarize the cutaneous toxicities associated with ADCs.
  • To provide guidance on recognizing and managing these dermatologic adverse events.

Main Methods:

  • Clinical review of approved ADCs and their associated toxicities.
  • Analysis of data from clinical trials and postmarketing studies.
  • Synthesis of current knowledge on ADC mechanisms and dermatologic side effects.

Main Results:

  • ADCs exhibit diverse mechanisms of action and indications for various cancers.
  • Unique and agent-specific cutaneous toxicities are frequently observed with ADCs.
  • Effective management strategies are crucial for patient tolerance and adherence.

Conclusions:

  • Dermatologists play a critical role in managing ADC-related skin toxicities.
  • Early recognition and appropriate intervention can mitigate adverse events.
  • This review provides essential guidance for clinicians managing patients on ADC therapy.

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