mTOR inhibitor-associated stomatitis (mIAS) in three patients with cancer treated with everolimus

Oral Surg Oral Med Oral Pathol Oral Radiol. 2015 Jan;119(1):e13-9. doi: 10.1016/j.oooo.2014.08.023. Epub 2014 Sep 16.

Abstract

Mammalian targets of rapamycin inhibitors (mTOR inhibitors, mTORI) are indicated for the management of several cancer types, including hormone receptor--positive or HER2-negative breast cancer, advanced renal cell carcinoma, advanced neuroendocrine tumors of pancreatic origin, and tuberous sclerosis complex-related tumors. Among the most common adverse events of mTORI medication are discrete, large, solitary or multiple, superficial ulcers, almost exclusively situated on nonkeratinized oral mucosa, described as mTORI-associated stomatitis (mIAS). We describe the clinical presentation, course, and management of mIAS in three patients receiving the mTORI everolimus (Afinitor, Novartis, East Hanover, NJ). In two patients, mIAS manifested 9 and 30 days after first using everolimus, respectively, whereas in the third patient, it recurred 3 months after re-introduction of everolimus. Oral rinses with a "magic mouthwash" solution (dexamethasone oral drops solution 2 mg/mL × 10 mL, lidocaine gel 2% × 30 g, doxycycline suspension 50 mg/5 mL × 60 mL, and sucralfate oral suspension 1000 mg/5 mL × 150 mL, dissolved in sodium chloride 0.9% × 2000 mL) four times daily proved helpful in alleviating the symptoms, and the ulcers healed in 4 to 15 days. No side effects were recorded, and dose reduction or discontinuation of everolimus was not necessitated in two cases.

Publication types

  • Case Reports

MeSH terms

  • Aged
  • Antineoplastic Agents / adverse effects*
  • Breast Neoplasms / drug therapy
  • Carcinoma, Renal Cell / drug therapy
  • Everolimus
  • Female
  • Humans
  • Kidney Neoplasms / drug therapy
  • Male
  • Middle Aged
  • Neoplasm Metastasis / drug therapy
  • Sirolimus / adverse effects
  • Sirolimus / analogs & derivatives*
  • Stomatitis / chemically induced*
  • Stomatitis / therapy

Substances

  • Antineoplastic Agents
  • Everolimus
  • Sirolimus