Comparison of tropisetron and chlorpromazine combinations in the control of nausea and vomiting in patients with advanced cancer
Comparison of tropisetron and chlorpromazine combinations in the control of nausea and vomiting in patients with advanced cancer
This single-institution, prospective, randomized trial was performed to evaluate the efficacy of tropisetron and chlorpromazine in the management of nausea and vomiting of terminal cancer patients. Patients had no recent chemotherapy or radiotherapy, and emesis was not due to bowel obstruction, electrolytic or metabolic disturbances, drug intake, or intracranial disease. One hundred and sixty patients randomly received either (a) chlorpromazine (CLO) (50 mg/day) plus dexamethasone (DEX) (2 mg/day), (b) chlorpromazine (25 mg/day) plus tropisetron (TRO) (5 mg/day), (c) chlorpromazine (25 mg/day) plus tropisetron (5 mg/day) plus dexamethasone (2 mg/day), or (d) tropisetron (TRO) (5 mg/day). Patients were monitored from day 1 to day 15. No nausea or vomiting was defined as “total” control. On day 15, total vomiting control was achieved in 33.3% of the patients receiving CLO + DEX, 84.6% of the patients receiving CLO + TRO, 92.5% of the patients receiving CLO + TRO + DEX, and 78.9% of the patients receiving TRO. Total control of nausea was achieved in 18.0% of the patients receiving CLO + DEX, 74.4% of the patients receiving (CLO + TRO), 85.0% of the patients receiving CLO + TRO + DEX, and 65.8% of the patients receiving TRO. Tropisetron-containing combinations produced significant control of nausea and vomiting from the third day onward. All antiemetic drugs were well tolerated. These data suggest that tropisetron-containing combinations or tropisetron as a single agent are much more effective in the control of emesis in patients with advanced cancer than the conventional antiemetic combination of chlorpromazine plus dexamethasone. Tropisetron is well tolerated and may be the best choice for controlling persistent nausea and vomiting in terminal cancer patients.
nausea, vomiting, emesis, far advanced cancer, tropisetron, chlorpromazine, dexamethasone
176-184
Mystakidou, Kyriaki
68283e0c-b4e5-4e3d-8775-40e48ef7620d
Befon, Sofia
9e9007c1-98fd-486b-9ad2-1e2e10ba7402
Liossi, Christina
fd401ad6-581a-4a31-a60b-f8671ffd3558
Vlachos, Lambros
9b2430fb-4cec-4b6d-b54f-f65dfbcaa89e
1998
Mystakidou, Kyriaki
68283e0c-b4e5-4e3d-8775-40e48ef7620d
Befon, Sofia
9e9007c1-98fd-486b-9ad2-1e2e10ba7402
Liossi, Christina
fd401ad6-581a-4a31-a60b-f8671ffd3558
Vlachos, Lambros
9b2430fb-4cec-4b6d-b54f-f65dfbcaa89e
Mystakidou, Kyriaki, Befon, Sofia, Liossi, Christina and Vlachos, Lambros
(1998)
Comparison of tropisetron and chlorpromazine combinations in the control of nausea and vomiting in patients with advanced cancer.
Journal of Pain and Symptom Management, 15 (3), .
(doi:10.1016/S0885-3924(97)00349-7).
Abstract
This single-institution, prospective, randomized trial was performed to evaluate the efficacy of tropisetron and chlorpromazine in the management of nausea and vomiting of terminal cancer patients. Patients had no recent chemotherapy or radiotherapy, and emesis was not due to bowel obstruction, electrolytic or metabolic disturbances, drug intake, or intracranial disease. One hundred and sixty patients randomly received either (a) chlorpromazine (CLO) (50 mg/day) plus dexamethasone (DEX) (2 mg/day), (b) chlorpromazine (25 mg/day) plus tropisetron (TRO) (5 mg/day), (c) chlorpromazine (25 mg/day) plus tropisetron (5 mg/day) plus dexamethasone (2 mg/day), or (d) tropisetron (TRO) (5 mg/day). Patients were monitored from day 1 to day 15. No nausea or vomiting was defined as “total” control. On day 15, total vomiting control was achieved in 33.3% of the patients receiving CLO + DEX, 84.6% of the patients receiving CLO + TRO, 92.5% of the patients receiving CLO + TRO + DEX, and 78.9% of the patients receiving TRO. Total control of nausea was achieved in 18.0% of the patients receiving CLO + DEX, 74.4% of the patients receiving (CLO + TRO), 85.0% of the patients receiving CLO + TRO + DEX, and 65.8% of the patients receiving TRO. Tropisetron-containing combinations produced significant control of nausea and vomiting from the third day onward. All antiemetic drugs were well tolerated. These data suggest that tropisetron-containing combinations or tropisetron as a single agent are much more effective in the control of emesis in patients with advanced cancer than the conventional antiemetic combination of chlorpromazine plus dexamethasone. Tropisetron is well tolerated and may be the best choice for controlling persistent nausea and vomiting in terminal cancer patients.
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Published date: 1998
Keywords:
nausea, vomiting, emesis, far advanced cancer, tropisetron, chlorpromazine, dexamethasone
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Local EPrints ID: 45056
URI: http://eprints.soton.ac.uk/id/eprint/45056
ISSN: 0885-3924
PURE UUID: bef2baa2-ac5e-4058-acfe-edc50a18cd72
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Date deposited: 26 Mar 2007
Last modified: 16 Mar 2024 03:48
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Author:
Kyriaki Mystakidou
Author:
Sofia Befon
Author:
Lambros Vlachos
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