K. Munstedt et al., Role of dexamethasone dosage in combination with 5-HT3 antagonists for prophylaxis of acute chemotherapy-induced nausea and vomiting, BR J CANC, 79(3-4), 1999, pp. 637-639
Dexamethasone (20 mg) or its equivalent in combination with 5-HT3 antagonis
ts appears to be the gold-standard dose for antiemetic prophylaxis. Additio
nal to concerns about the use of corticosteroids with respect to enhanced t
umour growth or impaired killing of the tumour cells, there is evidence tha
t high-dosage dexamethasone impairs the control of delayed nausea and emesi
s, whereas lower doses appear more beneficial. To come closer to the most a
dequate dose, we started a prospective, single-blind, randomized trial inve
stigating additional dosage of 8 or 20 mg dexamethasone to tropisetron (Nav
oban), a 5-HT3 receptor antagonist, in cis-platinum-containing chemotherapy
. After an interim analysis of 121 courses of chemotherapy in 69 patients,
we have been unable to detect major differences between both treatment alte
rnatives. High-dose dexamethasone (20 mg) had no advantage over medium-dose
dexamethasone with respect to objective and subjective parameters of acute
and delayed nausea and vomiting. In relation to concerns about the use of
corticosteroids in non-haematological cancer chemotherapy, we suggest that
8 mg or its equivalent should be used in combination with 5-HT3 antagonists
until further research proves otherwise.