Sorafenib and sunitinib: A dermatologist's perspective

Vijendran Pragasam1, Rajesh Verma1, Biju Vasudevan1

  • 1Department of Dermatology, Command Hospital, Pune, India.

Insights

Sorafenib and sunitinib, used for cancer treatment, can cause skin toxicities that disrupt patient care. This review covers the causes, effects, and management of these adverse skin reactions.

Area of Science:

  • Oncology
  • Dermatology
  • Pharmacology

Background:

  • Sorafenib and sunitinib are targeted therapies inhibiting tumor angiogenesis.
  • These drugs are used in treating renal cell carcinoma and hepatocellular carcinoma.
  • Cutaneous toxicities are common and can significantly impact treatment adherence.

Purpose of the Study:

  • To review the pathophysiology of drug-induced cutaneous toxicities.
  • To detail the adverse cutaneous effects and their grading.
  • To discuss management strategies for hand-foot skin reactions.

Main Methods:

  • Literature review of studies on sorafenib and sunitinib.
  • Analysis of pathophysiology and clinical presentation of skin toxicities.
  • Evaluation of risk factors and genetic influences.
  • Review of management and prevention strategies.

Main Results:

  • Cutaneous toxicities, including hand-foot skin reaction, are frequent side effects.
  • Severity can necessitate dose modification or treatment interruption.
  • Risk factors and genetic polymorphisms may influence toxicity development.
  • Early recognition and management are crucial.

Conclusions:

  • Understanding the mechanisms of cutaneous toxicity is key.
  • Effective management strategies can improve patient outcomes and treatment continuity.
  • Further research into predictive factors and targeted interventions is warranted.

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