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High-Dose Metoclopramide and Dexamethasone as an Antiemetic in Outpatients Receiving Chemotherapy for Breast Cancer
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Forty-six outpatients with breast cancer who had experienced severe emesis as a result of chemotherapy were evaluated for the antiemetic efficacy of high-dose metoclopramide (HD-MCP) and dexamethasone (DXM). Chemotherapy consisted of: cyclophosphamide 600, methotrexate 40 and 5-fluorouracil 600 mg/m2 (CMF) given intravenously every 3 weeks. The dosage of antiemetic drugs was MCP 2 mg/kg and DXM 0.2 mg/kg given by slow intravenous drip 0.5 h before the administration of chemotherapy. 138 courses of combined chemotherapy – HD-MCP and DXM – were administered, with a mean of 3 courses and a range of 1–10 courses per patient. Complete protection – no nausea and no vomiting – was achieved in 17.7% of the courses. Partial protection – no vomiting with mild nausea or 1–3 episodes of vomiting – in 45.3% of the courses. The total antiemetic efficacy was 63%. The most common side effects were: drowsiness, dry mouth, restlessness and diarrhea. Sixteen patients (35%) refused to continue the antiemetic regimen because of the side effects. HD-MCP and DXM have antiemetic efficacy, but because of these side effects, further studies are required to determine the optimal dose of each of these drugs.
Title: High-Dose Metoclopramide and Dexamethasone as an Antiemetic in Outpatients Receiving Chemotherapy for Breast Cancer
Description:
Forty-six outpatients with breast cancer who had experienced severe emesis as a result of chemotherapy were evaluated for the antiemetic efficacy of high-dose metoclopramide (HD-MCP) and dexamethasone (DXM).
Chemotherapy consisted of: cyclophosphamide 600, methotrexate 40 and 5-fluorouracil 600 mg/m2 (CMF) given intravenously every 3 weeks.
The dosage of antiemetic drugs was MCP 2 mg/kg and DXM 0.
2 mg/kg given by slow intravenous drip 0.
5 h before the administration of chemotherapy.
138 courses of combined chemotherapy – HD-MCP and DXM – were administered, with a mean of 3 courses and a range of 1–10 courses per patient.
Complete protection – no nausea and no vomiting – was achieved in 17.
7% of the courses.
Partial protection – no vomiting with mild nausea or 1–3 episodes of vomiting – in 45.
3% of the courses.
The total antiemetic efficacy was 63%.
The most common side effects were: drowsiness, dry mouth, restlessness and diarrhea.
Sixteen patients (35%) refused to continue the antiemetic regimen because of the side effects.
HD-MCP and DXM have antiemetic efficacy, but because of these side effects, further studies are required to determine the optimal dose of each of these drugs.
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