A. Markham et Em. Sorkin, ONDANSETRON - AN UPDATE OF ITS THERAPEUTIC USE IN CHEMOTHERAPY-INDUCED AND POSTOPERATIVE NAUSEA AND VOMITING, Drugs, 45(6), 1993, pp. 931-952
Ondansetron is a selective 5-HT3 receptor antagonist which has previou
sly been reported in the Journal to be a promising new agent for use a
s prophylaxis against nausea and vomiting caused by chemotherapy and r
adiotherapy. Since the publication of this original review, further st
udies have been published that show ondansetron to be an effective ant
iemetic agent in patients receiving chemotherapy and radiotherapy. Sev
eral studies have shown ondansetron to be a more effective antiemetic
agent than high-dose metoclopramide in patients with emesis induced by
high- and low-dose cisplatin treatment, and noncisplatin chemotherapy
-induced emesis. The drug as mono-therapy does not appear to offer any
advantage over alternative therapies against delayed high-dose cispla
tin-induced nausea and vomiting; however, extremely limited data sugge
st that ondansetron plus dexamethasone may be useful in this indicatio
n. Trials have shown combination therapy with ondansetron and dexameth
asone to be significantly more effective than both ondansetron monothe
rapy and a standard antiemetic regimen comprising metoclopramide, dexa
methasone and diphenhydramine against acute high-dose cis-platin-induc
ed emesis. Results from a number of small scale trials suggest that on
dansetron may be an effective treatment for chemotherapy-induced emesi
s refractory to conventional antiemetic therapy. Ondansetron also appe
ars to be more effective against refractory emesis induced by noncispl
atin chemotherapy than that induced by cisplatin chemotherapy. Several
trials have shown ondansetron to be more effective than placebo as pr
ophylaxis against postoperative nausea and vomiting; a further trial h
as shown single-dose ondansetron to be significantly more effective th
an single-dose droperidol or metoclopramide in this indication. In add
ition, several trials have shown ondansetron to be more effective than
placebo as treatment for nausea and vomiting that has commenced posto
peratively. The overall incidence of adverse events in ondansetron rec
ipients during chemotherapy-induced emesis studies was 36%. Headache a
nd constipation are the most common adverse events during ondansetron
therapy. Thus, recent data affirms the efficacy of ondansetron in the
treatment of acute chemotherapy-induced nausea and vomiting and shows
it to be especially efficacious when combined with dexamethasone. It a
ppears that the drug will also have a substantial role in the prophyla
xis and treatment of postoperative nausea and vomiting.