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Guidelines for Complications of Cancer Treatment Vol VIII Part B

Guidelines for Complications of Cancer Treatment Vol VIII Part B

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170to those that received placebo. However there wasno difference in the patient’s perception <strong>of</strong>xerostomia <strong>for</strong> patients receiving pilocarpine whencompared to the placebo arm. In two trialsconducted by Johnson and colleagues and LeVequeet al., significantly more patients treated withpilocarpine reported an improvement in xerostomiaas compared to the control group. In addition inthe study by LeVeque, there was a decrease in theuse <strong>of</strong> oral com<strong>for</strong>t agents in patients treated withpilocarpine.Based on the results <strong>of</strong> randomized trials theCCOPG (<strong>Cancer</strong> Care Ontario Practice<strong>Guidelines</strong>) arrived at a few suggestions regardingthe use <strong>of</strong> Pilocarpine in patients on radiotherapy,suffering from post radiotherapy xerostomia,provided there are no medical contra-indicationsto the use <strong>of</strong> pilocarpine. (2.5 – 10mg, bid or tiddosage). The exact duration <strong>of</strong> treatment is notknown. Other cholinergic agents with sialogogicproperties.Cevimeline - Studies are ongoing to evaluate its efficacy inxerostomia in Sjogrens’ syndrome.Radioprotectors like Amifostine:The FDA has approved the use <strong>of</strong> Amifostine <strong>for</strong>prevention <strong>of</strong> xerostomia in patients undergoingradiotherapy <strong>for</strong> the head and neck region. Thisrecommendation was based on the results <strong>of</strong> a phase IIIrandomized trial conducted by Brizel et al., whichrevealed that there was a decrease in the incidence <strong>of</strong>Grade 2 or higher chronic xerostomia from 57% to 34%in patients receiving amifostine. Also, there was no

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