[Oral toxicity of targeted anticancer therapies]

V Sibaud1, F Boralevi2, E Vigarios3

  • 1Dermatologie, consultation pluridisciplinaire de pathologie de la muqueuse buccale, institut universitaire du cancer, Toulouse Oncopole, 1, avenue Irene-Joliot-Curie, 31100 Toulouse cedex, France.

Insights

Targeted anticancer therapies can cause frequent oral side effects, including mucositis and hyperkeratosis. This study characterizes these common oral lesions, such as osteonecrosis of the jaw, associated with novel cancer treatments.

Area of Science:

  • Oncology
  • Oral Medicine
  • Dermatology

Background:

  • Targeted anticancer therapies are increasingly used, but their oral toxicities are not well-characterized.
  • Aphthous-like lesions from mTOR inhibitors are known, but other oral manifestations require detailed description.

Purpose of the Study:

  • To characterize the main oral lesions associated with targeted anticancer therapies.
  • To describe characteristic clinical manifestations of these novel drug classes.

Main Methods:

  • Review of clinical data and literature on oral toxicities of targeted anticancer therapies.
  • Description of specific oral lesions linked to drug classes like anti-EGFR, BRAF inhibitors, angiogenesis inhibitors, and imatinib.

Main Results:

  • Common oral lesions include mucositis (anti-EGFR), hyperkeratosis (BRAF inhibitors), and benign migratory glossitis.
  • Osteonecrosis of the jaw is observed with angiogenesis inhibitors; imatinib is linked to specific oral lesions.

Conclusions:

  • Targeted anticancer therapies induce a spectrum of oral toxicities beyond aphthous-like lesions.
  • Accurate characterization of these lesions is crucial for clinical management and patient care.

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