Effectiveness of cevimeline to improve oral health in patients with postradiation xerostomia

Head Neck. 2012 Aug;34(8):1136-42. doi: 10.1002/hed.21894. Epub 2012 Jan 9.

Abstract

Background: We assessed the effectiveness of cevimeline 30 mg 3 times daily in patient-reported oral health (Oral Health Impact Profile [OHIP-49]) and quality of life (QOL) in patients with xerostomia.

Methods: In our investigator-initiated, multicenter, randomized, double-blind, placebo-controlled study, patients who received >40 Gy of radiation therapy to the head and neck including at least 3 major salivary glands were randomized to cevimeline 30 mg or placebo orally 3 times daily for 6 weeks. Patients had to have grade 1 or 2 xerostomia and be >16 weeks posttreatment. Clinical data were collected and questionnaires administered at baseline and week 6. The primary outcome was change in OHIP-49 total score from baseline to week 6.

Results: No statistically significant differences in oral health or QOL were observed. During the 6 weeks of the study, the severity of xerostomia decreased from baseline.

Conclusions: Xerostomia is a significant sequela of treatment of head and neck cancer that may improve with time. The role of oral parasympathetic muscarinic secretogogues in alleviating patient symptoms and complaints remains unclear.

Publication types

  • Multicenter Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Carcinoma, Squamous Cell / radiotherapy
  • Double-Blind Method
  • Female
  • Head and Neck Neoplasms / radiotherapy
  • Humans
  • Male
  • Muscarinic Agonists / therapeutic use*
  • Oral Health*
  • Quality of Life
  • Quinuclidines / therapeutic use*
  • Radiotherapy / adverse effects*
  • Salivary Glands / radiation effects
  • Severity of Illness Index
  • Thiophenes / therapeutic use*
  • Xerostomia / drug therapy*
  • Xerostomia / etiology

Substances

  • Muscarinic Agonists
  • Quinuclidines
  • Thiophenes
  • cevimeline