Cutaneous toxicities of RAF inhibitors

Lancet Oncol. 2013 Jan;14(1):e11-8. doi: 10.1016/S1470-2045(12)70413-8.

Abstract

The RAF inhibitors vemurafenib and dabrafenib are emerging as the standard of care for Val600 BRAF-mutant metastatic melanoma. These drugs have shown clinical benefit over the standard care (dacarbazine); however, they are associated with frequent cutaneous adverse events, which can be concerning to the patient and their physician. Herein, we review the range of cutaneous disorders that seem to be induced by RAF inhibitors, including cutaneous squamous-cell carcinoma, hyperkeratotic lesions, Grover's disease, keratosis pilaris-like reactions, and photosensitivity. These disorders often affect patients' quality of life; therefore, dermatological assessment and timely management is essential to ensure that patients continue to use RAF inhibitors.

Publication types

  • Review

MeSH terms

  • Abnormalities, Multiple / chemically induced
  • Acantholysis / chemically induced
  • Acantholysis / pathology
  • Acantholysis / therapy
  • Antineoplastic Agents / administration & dosage
  • Antineoplastic Agents / adverse effects
  • Clinical Trials as Topic
  • Darier Disease / chemically induced
  • Eyebrows / abnormalities
  • Humans
  • Ichthyosis / chemically induced
  • Ichthyosis / pathology
  • Ichthyosis / therapy
  • Imidazoles / administration & dosage
  • Imidazoles / toxicity*
  • Indoles / administration & dosage
  • Indoles / toxicity*
  • Keratosis / chemically induced
  • Keratosis / pathology
  • Keratosis / therapy
  • Melanoma* / drug therapy
  • Melanoma* / pathology
  • Oximes / administration & dosage
  • Oximes / toxicity*
  • Photosensitivity Disorders / chemically induced
  • Photosensitivity Disorders / pathology
  • Photosensitivity Disorders / therapy
  • Proto-Oncogene Proteins B-raf* / antagonists & inhibitors
  • Proto-Oncogene Proteins B-raf* / genetics
  • Sulfonamides / administration & dosage
  • Sulfonamides / toxicity*
  • Vemurafenib

Substances

  • Antineoplastic Agents
  • Imidazoles
  • Indoles
  • Oximes
  • Sulfonamides
  • Vemurafenib
  • BRAF protein, human
  • Proto-Oncogene Proteins B-raf
  • dabrafenib

Supplementary concepts

  • Burnett Schwartz Berberian syndrome
  • Grover's disease