Efficacy of an ondansetron orally disintegrating tablet:: A novel oral formulation of this 5-HT3 receptor antagonist in the treatment of fractionated radiotherapy-induced nausea and emesis

被引:19
作者
LeBourgeois, JP
McKenna, CJ
Coster, B
Feyer, P
Franzén, L
Goedhals, L
Marzecki, Z
Souhami, L
Stewart, A
Tonnessen, F
Haigh, C
Mitchell, T
Wilkinson, JR
Graham, E
机构
[1] GlaxoWellcome Res & Dev, Oncol Clin Dev, Greenford UB6 0HE, Middx, England
[2] Hosp Henri Mondor, Creteil, France
[3] Hop St Joseph, Gilly, Belgium
[4] Free Univ Berlin, D-1000 Berlin, Germany
[5] Norrlands Univ Hosp, Umea, Sweden
[6] Natl Hosp, Bloemfontein, South Africa
[7] Pomeranian Med Acad, Szezecin, Poland
[8] Montreal Gen Hosp, Montreal, PQ H3G 1A4, Canada
[9] Christie Hosp NHS Trust, Manchester M20 4BX, Lancs, England
[10] Herlev Hosp, Copenhagen, Denmark
关键词
emesis; 5-HT3 receptor antagonist; nausea; ondansetron; orally disintegrating tablet; radiotherapy;
D O I
10.1053/clon.1999.9077
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A significant number of patients who are receiving radiotherapy experience the distressing side effects of emesis and nausea. Although prophylactic antiemetics are often given to patients who are receiving single-fraction, high-dose radiotherapy to the abdomen, a survey has revealed that antiemetic prophylaxis is not routinely offered to those receiving fractionated radiotherapy. Hence there is a need for an effective treatment of emesis for use in this group of patients. Ondansetron is an effective and well-tolerated antiemetic, which is used for the prevention of both chemotherapy and radiotherapy-induced emesis and nausea. This agent has been developed as a novel freeze-dried oral formulation. Ondansetron orally disintegrating tablets (ondODT) disperse rapidly when placed on the tongue. As the tablet does not need to be swallowed with water, it is a particularly useful formulation for patients who have difficulty with swallowing or who do not feel able to drink. This study was undertaken to investigate the efficacy of ondODT in the treatment of established emesis and nausea induced by radiotherapy. Two doses of ondODT, 8 mg and 16 mg, were compared with placebo in patients who developed emesis and/or moderate/severe nausea after receiving fractionated radiotherapy to sites located between the thorax and the pelvis. The study showed that ondODT was clinically superior to placebo in treating emesis and nausea successfully over a 12-hour period after taking the medication. There were no statistically significant differences between the two doses of ondODT. In the 2 hours after taking the study medication, patients who received ondODT (8 mg and 16 mg) had significantly fewer emetic episodes compared with those who received placebo. They also experienced significantly less nausea. In conclusion, ondODT 8 mg is effective in the treatment of radiotherapy-induced emesis and nausea and provides an effective alternative to the conventional ondansetron tablet.
引用
收藏
页码:340 / 347
页数:8
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