THE PREVENTION OF RADIOSURGERY-INDUCED NAUSEA AND VOMITING BY ONDANSETRON - EVIDENCE OF A DIRECT EFFECT ON THE CENTRAL-NERVOUS-SYSTEM CHEMORECEPTOR TRIGGER ZONE
S. Bodis et al., THE PREVENTION OF RADIOSURGERY-INDUCED NAUSEA AND VOMITING BY ONDANSETRON - EVIDENCE OF A DIRECT EFFECT ON THE CENTRAL-NERVOUS-SYSTEM CHEMORECEPTOR TRIGGER ZONE, Surgical neurology, 42(3), 1994, pp. 249-252
Nausea and emesis are significant side effects in patients undergoing
stereotactic radiosurgery for brain lesions in the region of the chemo
receptor trigger zone (area postrema of the brain). Even with the curr
ent antiemetic treatment (prochlorperazine +/- corticosteroids), those
side effects remain significant. The purpose of this study is twofold
: [1] to evaluate the efficacy of ondansetron in inhibiting nausea and
emesis in stereotactic radiosurgery patients and [2] to demonstrate t
hat ondansetron's locus of action is the central nervous system (CNS)
chemoreceptor trigger zone in the area postrema. In a pilot study, 10
patients receiving greater than or equal to 350 cGy in a single fracti
on of radiosurgery to the region of the area postrema received 32 mg o
ndansetron iv 1 hour prior to treatment +/- corticosteroids. In a retr
ospective analysis these results were compared to those of patients wi
th similar features (and matched for radiation dose to the area postre
ma and the dose of corticosteroids) who received prochlorperazine +/-
corticosteriods. Nine of 10 patients in the ondansetron group had no n
ausea or emesis within 48 hours after treatment; one patient experienc
ed one episode of emesis. In the prochlorperazine group, eight patient
s had symptoms, three patients needed hospitalization or a physician's
care for emesis within 24 hours, and five had nausea with no specific
treatment. These preliminary results suggest that ondansetron is a sa
fe and efficient drug to prevent nausea and emesis in this patient gro
up. The precise mechanism of action of ondansetron in these patients i
s unknown, but is likely due to the drug's serotonin-blocking effect w
ithin the CNS. A randomized, prospective study has been started at our
institution to confirm these preliminary results.