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Antiemetic activity of high-dose metoclopramide combined with methylprednisolone versus metoclopramide alone in dacarbazine-treated cancer patients. A randomized double-blind study of the Italian Oncology Group for Clinical Research
- Source :
- American journal of clinical oncology. 12(3)
- Publication Year :
- 1989
-
Abstract
- In a double-blind randomized trial, we compared the efficacy and tolerability of high-dose (2 mg/kg X 4) intravenous metoclopramide (MTC) versus metoclopramide plus high-dose (250 mg X 2) intravenous methylprednisolone (MP) administered for the first 2 days in untreated patients submitted to dacarbazine chemotherapy for 5 days. Thirty-four patients entered the study. Complete protection from nausea and vomiting was achieved in the majority of patients all through the study period with both antiemetic treatments, with slightly greater efficacy at day 2 for the combination. However, after suspension of the antiemetic therapy, there was a relapse of vomiting in patients. Side effects were not different between the two treatments, but extrapyramidal reactions were significantly increased on the second day of antiemetic therapy. In conclusion, high-dose MTC with or without MP can give good antiemetic protection and the combination seems to be slightly more efficacious. However, the relapse of vomiting after discontinuing antiemetic treatment and the high incidence of extrapyramidal reactions justify further studies to find a better antiemetic treatment.
- Subjects :
- Male
Cancer Research
Metoclopramide
Nausea
medicine.drug_class
Vomiting
medicine.medical_treatment
Methylprednisolone
law.invention
Random Allocation
Randomized controlled trial
Double-Blind Method
law
medicine
Antiemetic
Humans
Prospective Studies
Chemotherapy
business.industry
Middle Aged
Dacarbazine
Oncology
Tolerability
Anesthesia
Drug Therapy, Combination
Female
medicine.symptom
business
medicine.drug
Subjects
Details
- ISSN :
- 02773732
- Volume :
- 12
- Issue :
- 3
- Database :
- OpenAIRE
- Journal :
- American journal of clinical oncology
- Accession number :
- edsair.doi.dedup.....c3db8fa433bad15f071e67a6ebb90a17