Role of dexamethasone dosage in combination with 5-HT3 antagonists for prophylaxis of acute chemotherapy-induced nausea and vomiting

Citation
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
Citations number
17
Categorie Soggetti
Oncology,"Onconogenesis & Cancer Research
Journal title
BRITISH JOURNAL OF CANCER
ISSN journal
00070920 → ACNP
Volume
79
Issue
3-4
Year of publication
1999
Pages
637 - 639
Database
ISI
SICI code
0007-0920(199902)79:3-4<637:RODDIC>2.0.ZU;2-V
Abstract
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.