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Published on: January 7, 2015
[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.
Abstract:
While toxicity of targeted anticancer therapies on the oral mucosa seems relatively frequent in clinical practice, it has not been properly characterized to date, apart from aphthous-like lesions due to mTOR inhibitors. Herein, we report the main oral lesions associated with these new therapies, with a description of the most frequent but also the most characteristic clinical manifestations of these drugs, such as anti-EGFR-induced mucositis, BRAF-inhibitor-associated hyperkeratosis, benign migratory glossitis and osteonecrosis of the jaw observed with angiogenesis inhibitors, as well as lesions more specifically linked with imatinib.
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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